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Summary Literature (0)
DOID:0070096 - oculocutaneous albinism type II

Disease Ontology Definition:An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the OCA2 gene on chromosome 15q12-q13.

Synonyms: OCA2, Oculocutaneous Albinism, Tyrosinase-Positive

Xenbase Genes : oca2, mc1r

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008746 - oculocutaneous albinism type 2

MIM:
MIM:203200 - ALBINISM, OCULOCUTANEOUS, TYPE II; OCA2

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): oculocutaneous albinism (is_a)