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Disease Ontology Browser
hypotrichosis 13 (DOID:0110710)
Alliance: disease page
Synonyms: hypotrichosis with woolly hair; Hypt13
Alt IDs: OMIM:615896
Definition: A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the KRT71 gene on chromosome 12q13.13.

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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Send questions and comments to User Support. 		last database update
04/09/2024
MGI 6.23 		The Jackson Laboratory