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GENE - TERM ANNOTATION REPORT

55 Annotations Found.

An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by OMIM:300088


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by OMIM:300088
  • Original References(s): PMID:18414213


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by OMIM:300088
  • Original References(s): PMID:25741868


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by OMIM:300088
  • Original References(s): PMID:19752159


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by OMIM:300088
  • Original References(s): PMID:19214208


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: JUBERG-HELLMAN SYNDROME
  • Original References(s): PMID:18414213, PMID:26467025, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:22267240, PMID:22946748, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:28492532, PMID:29377098


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:25741868, PMID:28492532, PMID:28669061


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:18414213, PMID:25741868, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:25499160, PMID:26467025, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532, PMID:30287595


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:26467025, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:21480887, PMID:26993267, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:18234694, PMID:18469813, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: JUBERG-HELLMAN SYNDROME
  • Original References(s): PMID:23334464, PMID:25741868, PMID:26467025, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:28492532, PMID:30828795


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:28492532, PMID:29056246


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:25741868, PMID:28492532, PMID:30311386


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:20713952, PMID:21777234, PMID:22848613, PMID:28492532, PMID:29933521


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:28492532, PMID:29655203


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: JUBERG-HELLMAN SYNDROME
  • Original References(s): PMID:18414213, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:25326635, PMID:25741868


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: JUBERG-HELLMAN SYNDROME
  • Original References(s): PMID:18414213, PMID:19377476, PMID:22267240, PMID:26467025, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:18414213, PMID:25741868


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:22050978, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:21053371, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:20713952, PMID:22946748, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:26954813, PMID:28492532, PMID:29377098


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:22946748, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:18414213, PMID:19214208, PMID:19752159, PMID:20713952, PMID:25741868, PMID:26467025, PMID:28492532, PMID:29358611


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:21053371, PMID:22946748, PMID:27179713, PMID:27787195, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:22946748, PMID:27527380, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:26765483, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:23334464, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: JUBERG-HELLMAN SYNDROME
  • Original References(s): PMID:23066759, PMID:25741868, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: JUBERG-HELLMAN SYNDROME
  • Original References(s): PMID:22267240, PMID:25741868, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: JUBERG-HELLMAN SYNDROME
  • Original References(s): PMID:18469813, PMID:22267240, PMID:22946748, PMID:23334464, PMID:25741868, PMID:27143072, PMID:27527380, PMID:28492532, PMID:5116697


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:26544041, PMID:27527380, PMID:28492532, PMID:28837158, PMID:29377098, PMID:29655203


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: JUBERG-HELLMAN SYNDROME
  • Original References(s): PMID:22267240, PMID:22946748, PMID:23808377, PMID:25741868, PMID:27179713, PMID:27527380, PMID:28492532, PMID:29377098, PMID:29933145, PMID:30530412


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:20713952, PMID:25741868


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:25741868, PMID:31319225


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:22504056, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: JUBERG-HELLMAN SYNDROME
  • Original References(s): PMID:23334464, PMID:27527380, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:20713952, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: JUBERG-HELLMAN SYNDROME
  • Original References(s): PMID:23712037


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:23712037, PMID:27179713, PMID:28492532, PMID:29377098


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:20713952, PMID:21053371, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:23712037, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: JUBERG-HELLMAN SYNDROME
  • Original References(s): PMID:19214208, PMID:20713952, PMID:21480887, PMID:21519002, PMID:2267240, PMID:22848613, PMID:22946748, PMID:22949144, PMID:23334464, PMID:27527380, PMID:27787195, PMID:28492532


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:18234694, PMID:18469813


  • An association has been curated linking Pcdh19 and early infantile epileptic encephalopathy 9 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with PCDH19 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to early infantile epileptic encephalopathy 9  (DOID:0060848)
  • 4 papers in RGD have been used to annotate Pcdh19
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 9
  • Original References(s): PMID:22946748, PMID:25741868, PMID:27527380, PMID:28492532


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.