About   Help   FAQ
Disease Ontology Browser
hypotrichosis 8 (DOID:0110705)
Alliance: disease page
Synonyms: hypotrichosis, localized, autosomal recessive 3; Hypt8; Lah3
Alt IDs: OMIM:278150
Definition: A hypotrichosis has_material_basis_in a autosomal recessive mutation of LPAR6 on chromosome 13q14.2.

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