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Disease Ontology Browser
hypotrichosis 6 (DOID:0110703)
Alliance: disease page
Synonyms: autosomal recessive localized hypotrichosis; Hypotrichosis, Localized, Autosomal Recessive 1; Hypt6; Lah1; Monilethrix-like hypotrichosis
Alt IDs: OMIM:607903
Definition: A hypotrichosis that has_material_basis_in a autosomal recessive mutation of DSG4 on chromosome 18q12.1.

Disease References using Mouse Models (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
02/18/2020
MGI 6.14
The Jackson Laboratory