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Summary Literature (0)
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


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

Xenbase Genes : edar, edaradd

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant disease (is_a), hypohidrotic ectodermal dysplasia (is_a)