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Disease Ontology Browser
piebaldism (DOID:3263)
Alliance: disease page
Synonyms: Partial albinism; PIEBALD TRAIT
Alt IDs: OMIM:172800, ICD10CM:E70.39, MESH:D016116, NCI:C85009, ORDO:2884, UMLS_CUI:C0080024
Definition: An integumentary system disease characterized by congenital absence of melanocytes in areas of the skin and hair that has_material_basis_in heterozygous mutation in either KIT or SNAI2 on chromosome 4q12 or 8q11.21, respectively.

Disease References using Mouse Models (1)

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
11/15/2022
MGI 6.22
The Jackson Laboratory