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Disease Ontology Browser
oculocutaneous albinism (DOID:0050632)
Alliance: disease page
Alt IDs: ICD10CM:E70.3, MESH:D016115, OMIM:PS203100, ORDO:55
Definition: An autosomal recessive disease characterized by abnormal pigmentation of the skin, hair and eyes.

Disease References using Mouse Models (6)

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
10/08/2019
MGI 6.14
The Jackson Laboratory