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DO Term : ectodermal dysplasia 12 [DOID:0111652] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hypohidrotic ectodermal dysplasia that has_material_basis_in heterozygous mutation in the KDF1 gene on chromosome 1p36.11.

synonyms:
617337,
ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type,
OMIM:617337,
ECTD12

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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