| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | X-linked recessive ocular albinism (XLOA) is a rare disorder characterized by ocular hypopigmentation, foveal hypoplasia, nystagmus, photodysphoria, and reduced visual acuity in males. (Orphanet Rare Disease Ontology, Orphanet_54) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C537863 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Ocular Albinism type 1 from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| GPR143 | G protein-coupled receptor 143 | 2.88009 |
