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Disease Ontology Browser
hypotrichosis 1 (DOID:0110698)
Alliance: disease page
Synonyms: hereditary generalized hypotrichosis simplex; Hhs; Hts; Hypt1
Alt IDs: OMIM:605389
Definition: A hypotrichosis that has_material_basis_in a autosomal dominant mutation of APCDD1 on chromosome 18p11.22.


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
01/31/2023
MGI 6.22
The Jackson Laboratory