|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes/proteins associated with the disease Ocular Albinism type 1 from the curated CTD Gene-Disease Associations dataset.
|GPR143||G protein-coupled receptor 143||2.88009|