ectodermal dysplasia 10A

Summary

DOID:0111663 - ectodermal dysplasia 10A

Disease Ontology Definition:A hypohidrotic ectodermal dysplasia that has_material_basis_in heterozygous mutation in EDAR on chromosome 2q13.

Synonyms: ECTD10A, ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant

In OMIM:

OMIM:129490 - ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT; ECTD10A

OMIM:129490 - ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT; ECTD10A

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: edar, edaradd

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Parent(s): autosomal dominant disease (is_a), hypohidrotic ectodermal dysplasia (is_a)