|
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, Christ-Siemens-Touraine syndrome, ED1, HED1, X-linked anhidrotic ectodermal dysplasia, XHED, XLHED, ectodermal dysplasia 1, anhidrotic, ectodermal dysplasia 1, hypohidrotic, X-linked, ectodermal dysplasia 1, hypohidrotic/hair/tooth type, X-linked, hypohidrotic ectodermal dysplasia, X-Linked,
Xenbase Genes
:
eda
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hypohidrotic ectodermal dysplasia (is_a)