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| Term | Ambras type hypertrichosis universalis congenita | ID (Ontology) | DOID:0111060 (Human Disease) |
| 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. | ||
| Also Known As | "Ambras syndrome" ; "HTC1" | ||
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hair disease |__hypertrichosis |__Ambras type hypertrichosis universalis congenita |
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| Is a | hypertrichosis | ||
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GARD:8206 ICD10CM:Q84.2 MESH:C536605 MIM:145701 ORDO:1023 |
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