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Disease Ontology Browser
hypotrichosis 10 (DOID:0110707)
Alliance: disease page
Synonyms: Hypt10
Alt IDs: OMIM:614238
Definition: A hypotrichosis that has_material_basis_in an autosomal recessive mutation on chromosome 7p22.3-p21.3.

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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last database update
MGI 6.22
The Jackson Laboratory