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DO Term : hypotrichosis 1 [DOID:0110698] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the APCDD1 gene on chromosome 18p11.22.

synonyms:
HHS,
605389,
hereditary generalized hypotrichosis simplex,
OMIM:605389,
HYPT1,
HTS

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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