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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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.11
The Jackson Laboratory