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DO Term : hypotrichosis 2 [DOID:0110699] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the CDSN gene on chromosome 6p21.33.

synonyms:
Spanish type hypotrichosis,
146520,
OMIM:146520,
HTSS1,
HYPT2,
hypotrichosis simplex of the scalp 1

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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