Oculocutaneous albinism type 3 Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Type 3 oculocutaneous albinism (OCA3) is a form of oculocutaneous albinism (OCA; see this term) characterized by rufous or brown albinism and occurring mainly in the African population. (Orphanet Rare Disease Ontology, Orphanet_79433)
External Link http://www.omim.org/entry/203290
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Genes

1 genes associated with the Oculocutaneous albinism type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
TYRP1 tyrosinase-related protein 1