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Summary Literature (2)
DOID:0050632 - oculocutaneous albinism

Disease Ontology Definition:A syndrome characterized by abnormal pigmentation of the skin, hair and eyes.

Synonyms:

Xenbase Genes : slc24a5, slc45a2, lrmda, tyr, oca2, tyrp1, mc1r, abcc6

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018910 - oculocutaneous albinism


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), syndrome (is_a)