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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 TYRP1 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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last database update
10/15/2019
MGI 6.14
The Jackson Laboratory