About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory