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DO Term : hypotrichosis 4 [DOID:0110701] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hypotrichosis that has_material_basis_in a autosomal dominant mutation of HR on chromosome 8p21.3.

synonyms:
MUHH1,
Hypotrichosis, Marie Unna Type, 1,
OMIM:146550,
HYPT4,
Marie Unna Hereditary Hypotrichosis 1,
146550

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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