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Echinobase
Summary Literature (0)
DOID:0070097 - oculocutaneous albinism type III

Disease Ontology Definition:An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of TYRP1 on chromosome 9p23.

Synonyms: OCA3, Rufous Oculocutaneous Albinism,

Echinobase Genes :


OMIM:
MIM:203290 - albinism, oculocutaneous, type iii; oca3

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

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