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Disease Ontology Browser
oculocutaneous albinism type III (DOID:0070097)
Alliance: disease page
Synonyms: OCA3; Rufous Oculocutaneous Albinism
Alt IDs: OMIM:203290
Definition: An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the TYRP1 gene on chromosome 9p23.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory