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DO Term : hypotrichosis 12 [DOID:0110709] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the RPL21 gene on chromosome 13q12.2.

synonyms:
615885,
OMIM:615885,
HYPT12

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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