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RGD uses the Human Disease Ontology (DO, for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:cataract 39 multiple types
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Accession:DOID:0110236 term browser browse the term
Definition:A cataract that has_material_basis_in heterozygous mutation in the CRYGB gene on chromosome 2q34. (DO)
Synonyms:exact_synonym: CTRCT39;   autosomal dominant cataract 39 multiple types;   autosomal dominant cataract, multiple types 2
 primary_id: OMIM:615188
For additional species annotation, visit the Alliance of Genome Resources.

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cataract 39 multiple types term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Crygb crystallin, gamma B ISO ClinVar Annotator: match by OMIM:615188
ClinVar Annotator: match by term: Cataract 39, multiple types
PMID:23288985 PMID:28492532 NCBI chr 9:66,461,460...66,463,520
Ensembl chr 9:66,461,460...66,463,520
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17205
    sensory system disease 5611
      eye disease 2733
        lens disease 219
          cataract 212
            cataract 39 multiple types 1
Path 2
Term Annotations click to browse term
  disease 17205
    Developmental Disease 10918
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9457
        genetic disease 8960
          monogenic disease 7128
            autosomal genetic disease 6276
              autosomal dominant disease 4460
                cataract 39 multiple types 1
paths to the root