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Echinobase
Summary Literature (0)
DOID:0080614 - oculocutaneous albinism type VI

Disease Ontology Definition:An oculocutaneous albinism that has_material_basis_in an autosomal recessive null mutation of the SLC24A5 gene on chromosome 15q21.1.

Synonyms:

Echinobase Genes :


OMIM:
MIM:113750 - skin/hair/eye pigmentation, variation in, 4; shep4

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)