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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:0008746 - oculocutaneous albinism type 2 |
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)