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Summary Literature (0)
DOID:2121 - ectodermal dysplasia


Disease Ontology Definition:A syndrome characterized by abnormal development in 2 or more ectodermal structures (hair, nails, teeth, and sweat glands) without other systemic findings.

Synonyms: Congenital ectodermal defect, Congenital ectodermal defect (disorder), Congenital ectodermal dysplasia, Ectodermal dysplasia (disorder)

Xenbase Genes : wnt10a, hoxc13, tp63, kremen1, cdh3, smarcad1, ctsc, edar, ikbkg, edaradd, kdf1, kctd1, eda, col11a1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019287 - ectodermal dysplasia syndrome


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

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