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.