About   Help   FAQ
Disease Ontology Browser
hypotrichosis 7 (DOID:0110704)
Alliance: disease page
Synonyms: hypotrichosis, localized, autosomal recessive 2; Hypt7; Lah2; total Mari type hypotrichosis,
Alt IDs: OMIM:604379
Definition: A hypotrichosis that has_material_basis_in a autosomal recessive mutation of the LIPH gene on chromosome 3q27.2.


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, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory