Oculocutaneous albinism type 1B Gene Set

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
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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