| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Oculocutaneous albinism type 1B (OCA1B) is a type of OCA1 (see this term) characterized by skin and hair hypopigmentation, nystagmus, reduced iris and retinal pigment and misrouting of the optic nerves. (Orphanet Rare Disease Ontology, Orphanet_79434) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C537729 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Oculocutaneous albinism type 1B from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| TYR | tyrosinase | 2.88009 |
