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GENE - TERM ANNOTATION REPORT

279 Annotations Found.

An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11609659 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11593686 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11586736 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151793612 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151876244 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151861471 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126920221 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151880633 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151763770 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:16199547 PMID:16951682 PMID:21911699 PMID:22749724 PMID:23998934 PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11609477 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15146564 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11649366 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127303158 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13474261 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11659777 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15183274 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15135418 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11660978 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11647203 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11602382 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15134021 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12913250 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11602281 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127293740 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15151688 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11658251 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15140192 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11606132 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13504392 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15105607 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151876147 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11663801 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13616368 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26922723 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127275473 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8556047 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:16951682 PMID:20301737


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8556048 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:16951682 PMID:20301737 PMID:21911699


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11591564 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11601598 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8556049 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:16951682 PMID:20301737


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11583148 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151804670 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11607458 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11662827 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11603044 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11653382 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11596079 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11606786 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11654443 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11593232 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11605899 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11605383 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11607755 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11603844 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11611748 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11648544 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11610159 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11609394 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11659351 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11650571 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11598089 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11605064 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11612290 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11654960 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11664019 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11610264 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11611113 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11651749 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11606444 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11583989 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11608641 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11601326 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11610671 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11610731 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11606747 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11657662 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11589582 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11610496 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11663785 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11657093 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11609862 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11663033 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11608335 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11584803 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11645406 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11603883 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11605340 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13480110 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11603156 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8567020 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:17928815 PMID:20301737


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11648476 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11596953 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28869650 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8567021 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127266541 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13616366 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127231196 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13818717 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13821107 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11600222 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15119814 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11607330 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14695696 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:25741868


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12850099 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:25741868


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905463 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28873511 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28867251 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11609149 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28869412 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28873514 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905273 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905281 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910449 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905666 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905670 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905275 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905278 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28873760 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28873505 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910584 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150429470 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150429471 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910589 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910445 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910587 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28869178 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28873764 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905673 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28908242 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910447 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910726 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28908253 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28869410 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28874022 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15139381 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28908240 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910721 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910585 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28908238 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28905461 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13211722 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28873507 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28874024 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28869405 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28869176 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28869407 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156351085 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11601841 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152037001 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11584701 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152109520 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152137978 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152078287 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152059874 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152141227 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152121583 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152036162 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152140588 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152079191 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152148255 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152073980 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152052978 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28869656 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152119052 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152107714 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11605522 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15198169 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152026213 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152109158 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152078138 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152077386 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152036763 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152128982 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152050257 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152069540 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152156548 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152089721 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152140909 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152061805 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156228235 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152977803 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:25741868


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:329846785 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28874250 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28869654 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:329952049 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126743229 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:25741868


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:405030477 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151780559 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13481573 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:21911699 PMID:22749724 PMID:23998934 PMID:25741868 PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151719980 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151764166 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151789453 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151861703 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151709119 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126743225 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151866714 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151844456 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151758047 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11590278 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151836886 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151835537 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151854157 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151839039 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151750928 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:16199547 PMID:21911699 PMID:22749724 PMID:23998934 PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21069490 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15102705 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156018177 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156358477 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156438910 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910724 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156437775 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:18022865 PMID:20513915 PMID:21911699 PMID:22184204 PMID:22749724 PMID:23998934 PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156447003 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156248109 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15114574 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15163896 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156354636 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156097764 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156010290 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:16199547 PMID:21911699 PMID:22749724 PMID:23998934 PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156140790 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156216570 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156039353 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156048614 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155906084 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155935758 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156094852 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156075967 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156409195 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11598815 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155974791 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156413240 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156110089 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:405035100 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155925708 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156094824 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156040170 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155938778 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11604118 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156022450 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11597106 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156139423 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155939321 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156296998 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156113140 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156157643 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151762501 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:21911699 PMID:22749724 PMID:23998934 PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156367493 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156113836 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156294854 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156105486 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156026999 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156379669 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155910372 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127289529 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150491736 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156202378 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156119552 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155957939 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156351930 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156211261 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151348289 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:21911699 PMID:22749724 PMID:23998934 PMID:25741868 PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156284141 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156370545 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155948222 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156143229 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156297071 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156292778 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156111478 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 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
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:405020434 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:405011765 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11606533 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:405023730 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:404977043 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402500667 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402504133 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:402520515 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:405012119 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking HYCC1 and hypomyelinating leukodystrophy 5 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:405025655 (Homo sapiens)
  • 11 RGD objects have been annotated to hypomyelinating leukodystrophy 5  (DOID:0060793)
  • 4 papers in RGD have been used to annotate HYCC1
  • Curation Notes: ClinVar Annotator: match by term: Hypomyelination and Congenital Cataract
  • Original References(s): PMID:28492532


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