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Summary Literature (0)
DOID:0111664 - ectodermal dysplasia 1

Disease Ontology Definition:A hypohidrotic ectodermal dysplasia that has_material_basis_in X-linked recessive mutation in EDA on chromosome Xq13.1.

Synonyms: CST syndrome, ectodermal dysplasia 1, anhidrotic, ED1, HED1, hypohidrotic ectodermal dysplasia, X-Linked, X-linked anhidrotic ectodermal dysplasia, XHED, Christ-Siemens-Touraine syndrome, ectodermal dysplasia 1, hypohidrotic, X-linked, ectodermal dysplasia 1, hypohidrotic/hair/tooth type, X-linked, XLHED

Xenbase Genes : eda


MIM:
MIM:305100 - ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): hypohidrotic ectodermal dysplasia (is_a), X-linked recessive disease (is_a)