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DOID:0070099 - oculocutaneous albinism type V
Disease Ontology Definition:An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the OCA5 gene on chromosome 4q24.
Synonyms: OCA5,
Xenbase Genes :
MONDO:0014127 - oculocutaneous albinism type 5 |
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)