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Summary Literature (0)
DOID:0111653 - ectodermal dysplasia 11A


Disease Ontology Definition:A hypohidrotic ectodermal dysplasia that has_material_basis_in heterozygous mutation in EDARADD on chromosome 1q42-q43.

Synonyms: ECTD11A, ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant

In OMIM:
OMIM:614940 - ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT; ECTD11A


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

Xenbase Genes : edaradd

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