About   Help   FAQ
Disease Ontology Browser
hypotrichosis 9 (DOID:0110706)
Alliance: disease page
Synonyms: Hypt9
Alt IDs: OMIM:614237
Definition: A hypotrichosis that has_material_basis_in an autosomal recessive mutation on chromosome 10q11.23-q22.3.

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 & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.17
The Jackson Laboratory