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Disease Ontology Browser
hypotrichosis 5 (DOID:0110702)
Alliance: disease page
Synonyms: HYPT5; Marie Unna Hereditary Hypotrichosis 2; MUHH2
Alt IDs: OMIM:612841, MESH:C567554
Definition: A hypotrichosis that has_material_basis_in a mutation on chromosome 1p21.1-q21.3.

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
12/10/2024
MGI 6.24 		The Jackson Laboratory