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Summary Literature (0)
DOID:0070098 - oculocutaneous albinism type IV

Disease Ontology Definition:An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the SLC45A2 gene on chromosome 5p13.2.

Synonyms: OCA4

Xenbase Genes : slc45a2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011683 - oculocutaneous albinism type 4


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)