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Summary Literature (0)
DOID:14793 - hypohidrotic ectodermal dysplasia

Disease Ontology Definition:An ectodermal dysplasia that is characterized by malformation of ectodermal (skin, hair, teeth and sweat glands) structures including hypotrichosis (sparseness of scalp and body hair), hypohidrosis (reduced ability to sweat), and hypodontia (congenital absence of teeth).

Synonyms: Christ-Siemens-Touraine Syndrome, Ectodermal Dysplasia 1, Anhydrotic, Hypohidrotic X-linked ectodermal dysplasia, Hypohidrotic X-linked ectodermal dysplasia (disorder), anhidrotic ectodermal dysplasia 3,

Xenbase Genes : edar, ikbkg, edaradd, kdf1, eda

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0016535 - hypohidrotic ectodermal dysplasia


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Clouston syndrome (is_a), ectodermal dysplasia (is_a)