Ocular Albinism type 1 Gene Set

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
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Genes

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