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Summary Literature (0)
DOID:0070100 - oculocutaneous albinism type VII

Disease Ontology Definition:An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of C10orf11 on chromosome 10q22.2-q22.3.

Synonyms: OCA7,

Xenbase Genes : lrmda

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014070 - oculocutaneous albinism type 7


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)