| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Type 1 oculocutaneous albinism (OCA1) describes a group of tyrosine related OCAs (see this term) that includes OCA1A, OCA1B, type 1 minimal pigment oculocutaneous albinism (OCA1-MP) and type 1 temperature sensitive oculocutaneous albinism (OCA1-TS) (see these terms). (Orphanet Rare Disease Ontology, Orphanet_352731) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C537728 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Oculocutaneous albinism type 1 from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| TYR | tyrosinase | 2.88009 |
