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Summary Literature (0)
DOID:0111060 - Ambras type hypertrichosis universalis congenita

Disease Ontology 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.

Synonyms: Ambras syndrome, HTC1,

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007787 - Ambras type hypertrichosis universalis congenita


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hypertrichosis (is_a)