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DO Term : Ambras type hypertrichosis universalis congenita [DOID:0111060] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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:
  • OMIM:145701,
  • Ambras syndrome,
  • HTC1,
  • GARD:8206,
  • 145701,
  • ICD10CM:Q84.2,
  • ORDO:1023,
  • MESH:C536605
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents