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Disease Ontology Browser
hypotrichosis 2 (DOID:0110699)
Alliance: disease page
Synonyms: Htss1; hypotrichosis simplex of the scalp 1; Hypt2; Spanish type hypotrichosis
Alt IDs: OMIM:146520
Definition: A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the CDSN gene on chromosome 6p21.33.

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
04/16/2024
MGI 6.23 		The Jackson Laboratory