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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 the EDARADD gene on chromosome 1q42-q43.

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

Xenbase Genes : edaradd


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

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), hypohidrotic ectodermal dysplasia (is_a)