|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes/proteins associated with the disease Oculocutaneous albinism type 1B from the curated CTD Gene-Disease Associations dataset.