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DO Term : hypotrichosis 5 [DOID:0110702] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hypotrichosis that has_material_basis_in a mutation on chromosome 1p21.1-q21.3.
  • synonyms:
  • HYPT5,
  • MUHH2,
  • 612841,
  • OMIM:612841,
  • MESH:C567554,
  • Marie Unna Hereditary Hypotrichosis 2
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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





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