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Disease Ontology Browser
Ambras type hypertrichosis universalis congenita (DOID:0111060)
Alliance: disease page
Synonyms: Ambras syndrome; HTC1
Alt IDs: OMIM:145701, ICD10CM:Q84.2, MESH:C536605, ORDO:1023
Definition: A hypertrichosis characterized by autosomal dominant inheritance of the presence of vellus-type hair on the entire body, especially on the face, ears and shoulders, with the exception of palms, soles, and mucous membranes that has_material_basis_in chromosomal abnormalities in the region 8q22.

Disease References using Mouse Models (1)
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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12/10/2024
MGI 6.24 		The Jackson Laboratory