Term Name:	Ambras type hypertrichosis universalis congenita
Synonyms:	Ambras syndrome, HTC1
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.
Ontology:	Human Disease [DOID:0111060]   ( DOID:0111060 )