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GENE - TERM ANNOTATION REPORT

988 Annotations Found.

An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155710785 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156040105 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156284383 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10448538 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:26463574


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10448537 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:26463574


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13475212 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126727794 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:16199547 PMID:24781755 PMID:25741868 PMID:26463574 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13527853 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156289550 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13704898 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151779434 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15173914 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156085932 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156400596 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156277413 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152108305 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151890092 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151763416 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38458738 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689509 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156204507 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156305097 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24781755 PMID:26463574 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151751029 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151865772 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152047739 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152049841 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11596795 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152118241 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127271861 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9687651 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156000179 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151791567 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151731735 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127313084 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151712546 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151760976 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127335100 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151823770 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14719247 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151762860 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152062116 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151355913 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151730623 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151817042 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151866066 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126764894 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127332307 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151710590 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152109793 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151767202 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26918440 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152113602 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151876308 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152086901 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150494496 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151756251 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152056330 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152131538 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152030344 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151773917 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9690500 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126916875 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13624879 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151712718 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126769499 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15173016 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152034757 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151778034 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156402773 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13624881 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579591 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152111974 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608051 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126766860 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126745534 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152113803 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151757836 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127310171 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151866059 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152055248 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126732943 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152028340 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151842938 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151829597 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151873247 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13806557 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13490857 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26898011 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151806989 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151750242 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151871557 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152083761 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11638797 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152078176 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152026454 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126772398 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126735100 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152058519 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691533 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13473333 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152075347 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11592509 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151736844 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26920779 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151800985 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151834535 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152069919 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38458193 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13539488 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151753567 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152081094 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151831428 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152066385 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151884689 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127304643 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13821100 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127248997 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151872159 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152160984 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151802332 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151731068 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151754136 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151793695 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13473905 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38466423 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152038181 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151834635 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15114072 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151842606 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38467713 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151850425 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38465402 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152118667 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15131902 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151886991 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152168999 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28902563 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152046953 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151783819 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151767634 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151853215 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:16199547 PMID:24781755 PMID:26463574 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151797050 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127263566 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13477473 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127277825 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152105066 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38461738 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152094175 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152169505 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127312121 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152123605 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127276613 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152027438 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151796565 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13487087 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152108882 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151816637 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26888915 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151849383 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38463866 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152051328 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126751272 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608048 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26892972 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152029868 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152106959 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151867592 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14744749 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151884434 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14710806 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13624882 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11596966 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152122475 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38469167 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151783605 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151739616 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11094463 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11584897 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126759543 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152050088 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15158947 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152071646 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126732001 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152116955 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126770805 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126754205 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15202405 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9690264 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38456764 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152065018 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151734710 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151814278 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11652591 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13624872 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15129076 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152088875 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691536 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9690508 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150424914 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152076915 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151754823 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152060749 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9687654 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26916243 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24781755 PMID:26463574 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127303102 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151827107 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38472558 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152164643 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13464734 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151716623 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152056675 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14718507 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127231016 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151826212 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152081602 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152163207 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151761471 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152028483 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151788472 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26903372 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126921675 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126750451 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26920484 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151882474 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152157192 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8559984 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9360932 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151841618 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13491201 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152107468 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151820243 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127271994 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151724630 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38460214 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151733708 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127233102 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151780537 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127249805 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151761564 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13624878 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13624889 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126773168 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14701567 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151827816 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151816324 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152078761 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127271442 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151794526 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126763891 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127248817 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151837606 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26920275 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151753311 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14731169 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26917960 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151834317 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152085587 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151748431 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151851010 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126914377 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152138770 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151831303 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24781755 PMID:26463574 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13536980 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26904674 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151872629 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608050 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127232220 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151727781 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152095649 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151860344 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151819720 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126922725 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152167421 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151885146 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151816025 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152105320 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151746588 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152156323 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152130320 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152074276 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152031121 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151893391 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24781755 PMID:26463574 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13624884 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151807450 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15186803 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126921755 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14704474 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151750826 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127315893 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152035874 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126732735 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152086661 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11093054 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152167484 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152033653 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151849857 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126726727 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152104975 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151755862 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151760237 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152135598 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14704426 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10050358 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152033294 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151854923 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152110881 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151855995 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151758906 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152161744 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152155155 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151858659 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38468073 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151798489 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15125790 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38456180 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152048882 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152034584 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38467278 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13624888 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152109496 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11598248 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152125956 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152132693 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152143638 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14744822 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608049 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13491195 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152170964 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151744687 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152042591 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152148372 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152172825 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152133850 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152054717 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151878103 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152098787 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152109619 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151890683 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151824519 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126745777 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11641725 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152171963 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151779002 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13815730 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152113652 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15174365 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11586134 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15146888 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15188466 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26919750 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15122347 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151767918 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26887491 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38457487 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14745159 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13817671 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127259521 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152061646 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152141401 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152029193 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126736348 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13805175 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127312427 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15133393 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152173955 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151791670 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126747976 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151848159 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151818658 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126757865 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152103377 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151734385 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127239367 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24781755 PMID:26463574 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126910678 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532 PMID:30311386


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38470618 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127302653 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151855527 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156137528 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126727777 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152071366 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151808983 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13445893 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532 PMID:30311386


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151799821 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152129440 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150540664 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126745213 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126919760 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151744345 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152122222 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152122815 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691531 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15141642 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152161798 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127309507 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13624876 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151756500 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689750 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151818584 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13801414 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126733644 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26912086 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13808593 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151769151 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127237049 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127322392 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151757982 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151734296 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13472062 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11094926 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11584065 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15155297 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151724667 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11587329 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152127032 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152114882 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151752803 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151736954 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11593493 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:23804846 PMID:24033266 PMID:26011067 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151777539 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11092248 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152067739 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127263918 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13473926 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15107057 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151737941 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152147308 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151765666 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15125795 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152049385 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151710289 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689508 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126743368 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126755915 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151884858 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151847935 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152159516 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151864994 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127331354 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152143435 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151824087 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14723478 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15181619 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152135937 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13486121 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152038436 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151717828 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152049880 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152038009 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152032397 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127306583 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152161503 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14736254 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14705631 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151865439 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127293159 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152132934 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151771693 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151871308 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24781755 PMID:26463574 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152169943 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152092822 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11585515 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:22938506 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151871374 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127274901 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26918528 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151878705 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152101533 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38459267 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152133440 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38466921 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151747625 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127306707 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126753558 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127245069 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13808020 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38456176 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13813425 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152155421 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127276191 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38468891 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151722639 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152100621 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152174816 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13624874 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8608047 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38472658 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14726271 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151835755 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14734051 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151790798 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15135785 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152125801 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15115000 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151831869 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151855967 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151734065 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152123267 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13475661 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26892384 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127298747 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127273198 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24781755 PMID:26463574 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15179193 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14729227 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151846238 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151789999 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151736010 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127255190 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126919121 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28902773 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13811668 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127336493 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11641381 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126746572 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8625944 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11595890 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152027810 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151874068 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152135904 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26921790 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151790374 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38468802 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28888605 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151726408 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532 PMID:35307828


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151852425 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127304185 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38457332 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15125736 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151852048 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152153734 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151798418 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151736972 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38457410 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127262708 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152071998 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151755972 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127325940 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38465022 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38459565 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14733343 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28891867 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127256572 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14701581 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13537896 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152146237 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150424954 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126732889 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151760113 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151783936 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152126149 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26914277 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151868053 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152108519 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151870250 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151856669 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13624880 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38468598 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151868098 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152136941 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127282827 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151832261 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151773884 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151773037 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127287179 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151782215 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152168911 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152035759 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11597803 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15129210 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152085053 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11592201 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151805301 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151727152 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152062949 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13624873 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151738515 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151838158 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151877933 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151854198 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151881910 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13216061 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151810799 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127269631 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152033081 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152072218 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11590479 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151848561 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127252326 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689749 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151833341 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9687652 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127288952 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151716918 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151774696 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13470783 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126728415 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152113951 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151876488 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24781755 PMID:26463574 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152162479 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13624930 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152135051 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127334583 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13624887 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26906854 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151872435 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11092854 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151782351 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13624883 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151848596 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11588290 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151740828 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14729007 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38469033 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127332124 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152056697 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152141398 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127281264 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152121312 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152090794 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151875785 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152137473 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151784423 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152174071 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151796047 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127319253 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151877159 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13624885 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151737134 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151859791 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151742883 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152118210 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11093269 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127273339 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126754974 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151870774 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152174684 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11088841 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:23804846 PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156194084 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151874820 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151749540 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151804832 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151831720 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13817871 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126752605 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152161296 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151892738 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152169074 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14716480 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11581681 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13537904 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150488263 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26890516 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24781755 PMID:26463574 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156386822 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156244648 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13818315 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152978282 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13487744 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532 PMID:30896630


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155931371 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155992291 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156287914 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11547259 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156403149 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156159147 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9850355 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24781755 PMID:25558065 PMID:25741868


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13821912 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156022290 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155943157 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402513230 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155910574 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24781755 PMID:26463574 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156440607 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156128862 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156234867 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155977496 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156149952 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155997884 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14742470 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156382642 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156114613 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155709352 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155709401 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155709612 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155709485 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155711032 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155710882 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155710866 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155708876 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155709938 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155709830 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155710296 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155709527 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155708631 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155709004 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155710990 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155710917 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155709638 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155708988 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155710705 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156438489 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156136201 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24781755 PMID:26463574 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156023141 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156323009 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156364428 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156436041 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156436740 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156440195 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126919478 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156447008 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127335623 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38598630 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13801525 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13537295 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127313231 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156411298 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156372867 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156441898 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156204937 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156157339 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155975215 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155964471 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156091961 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156153320 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156078346 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156270737 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156441511 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156246300 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156039888 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156124481 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156153657 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156195161 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155953060 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156315346 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156175925 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156212970 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156191077 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156286027 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155944673 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156176056 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156220230 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156297568 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156269469 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155992961 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156378314 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156058509 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156075121 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156021027 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156168222 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156252141 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156241865 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156033248 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156043043 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156362211 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156415482 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156068236 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156143104 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156285909 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156206332 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156403426 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155910011 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156313121 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156155615 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156268523 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156110444 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156184670 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156325717 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155913030 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156151094 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156118032 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156148724 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156088302 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156131247 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156187614 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156382834 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156006534 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155990334 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11594739 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156031320 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156352616 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156342183 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155942804 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156299952 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156358854 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156107014 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156360895 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156302343 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156021648 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156308199 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156084911 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156232377 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156319430 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156394935 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156221599 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156373287 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155992840 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155992552 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156190046 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156025949 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156264553 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156055235 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156121939 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156291941 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11090437 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26912466 PMID:27707755 PMID:27808407 PMID:27911912 PMID:28492532 PMID:28815995 PMID:28983057 PMID:32678080


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156127175 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156379313 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155981200 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156290584 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155934825 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150548574 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156311574 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156299389 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156352935 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156109413 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156236911 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156228099 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156181123 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156281005 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156340027 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156016742 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155978916 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15176078 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155942787 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156011706 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156233288 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155998371 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156356650 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156161732 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155922030 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156344375 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156294715 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155949847 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156278099 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155998963 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156079379 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156314087 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155921730 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156379485 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156005438 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156205825 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156299194 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156326055 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156012169 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156011729 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156037830 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156014805 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155924703 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156095367 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156265926 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156384705 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156268321 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156394304 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15185677 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155991156 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155977171 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156159359 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156134432 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155913314 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155986622 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156265359 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156217528 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156407046 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155996883 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156108781 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155974922 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155934062 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156365153 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155909756 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156208905 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156393840 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156267479 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156322211 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155992296 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156238811 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11595766 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156190515 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:16199547 PMID:24781755 PMID:26463574 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156026279 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156381775 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13525053 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:24033266 PMID:28492532 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156389375 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156413914 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155946887 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155956874 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156122139 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151888263 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:16199547 PMID:24781755 PMID:26463574 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156309606 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156051986 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155947527 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156294877 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156006173 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155949956 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151828897 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:16199547 PMID:24781755 PMID:26463574 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155942778 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156220122 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155981917 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156005441 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156113089 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156073291 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150549404 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156374100 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155959383 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156190175 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155901414 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156218082 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11643530 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156200124 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156364055 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155936864 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156385659 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24781755 PMID:26463574 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156090307 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155944704 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11641602 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156217339 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155975247 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156123609 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156220797 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150553743 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156115161 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156040276 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156073637 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156065846 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38460383 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156334530 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156355769 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155926780 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155935539 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155931530 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156309776 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24781755 PMID:26463574 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156326319 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156215612 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156174492 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156194682 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156402939 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155912407 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155800581 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred from experiment (EXP)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155266814 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9687653 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151777444 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14711236 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13471429 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25342930 PMID:25741868 PMID:27808407 PMID:28492532 PMID:34279089


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151876703 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28898597 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21404697 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532 PMID:30311386


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402498057 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38456319 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24781755 PMID:26463574 PMID:28492532 PMID:29758562


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402490606 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151823975 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24781755 PMID:26463574 PMID:28492532 PMID:33176815


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:401860958 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402496846 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402508366 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402487265 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402492158 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402502726 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28888267 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402497444 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402490725 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402494669 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402514073 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402515675 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402522426 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402510352 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402516241 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402509106 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402515287 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38462939 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402509301 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402520323 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402513522 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402509646 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28896434 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402491212 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402516255 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151735033 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532 PMID:33229591


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11646992 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402502399 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402504645 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402492185 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402498835 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402515588 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402515823 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402523559 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402520344 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28898600 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402496855 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402504478 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402506313 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402505938 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402484244 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402504881 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691532 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402495958 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking DIAPH1 and Seizures, Cortical Blindness, and Microcephaly Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402508536 (Homo sapiens)
  • 3 RGD objects have been annotated to Seizures, Cortical Blindness, and Microcephaly Syndrome  (DOID:9005489)
  • 8 papers in RGD have been used to annotate DIAPH1
  • Curation Notes: ClinVar Annotator: match by term: Seizures, cortical blindness, and microcephaly syndrome
  • Original References(s): PMID:28492532


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