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DOID:0070097 - oculocutaneous albinism type III
Disease Ontology Definition:An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the TYRP1 gene on chromosome 9p23.
Synonyms: OCA3, Rufous Oculocutaneous Albinism,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0008747 - oculocutaneous albinism type 3 |
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)