| 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 |
| Similar Terms | |
| Downloads & Tools |
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 |
