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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 the LPAR6 gene 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)
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last database update
MGI 6.22
The Jackson Laboratory