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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 OCA2 on chromosome 15q12-q13.

Synonyms: OCA2; Oculocutaneous Albinism, Tyrosinase-Positive

Referenced OMIM:

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : oca2, mc1r

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): oculocutaneous albinism (is_a)

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