| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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://ctdbase.org/detail.go?type=disease&acc=MESH:C537731 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Oculocutaneous albinism type 3 from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| TYRP1 | tyrosinase-related protein 1 | 2.88009 |
