An X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ECTODYSPLASIN.
Also Known As:
Ectodermal Dysplasia 1, Anhidrotic; Anhidrotic Ectodermal Dysplasia, X-Linked; Anhydrotic Ectodermal Dysplasia, X-Linked; CST Syndrome; Ectodermal Dysplasia 1; Ectodermal Dysplasia 1, Anhydrotic; Ectodermal Dysplasia, Anhidrotic, X-Linked; Ectodermal Dysplasia, Hypohidrotic, X-Linked; Ectodermal Dysplasia, Hypohydridic, X-Linked; Hypohidrotic Ectodermal Dysplasia; X-Linked Hypohydridic Ectodermal Dysplasia; Anhidrotic Ectodermal Dysplasia, X Linked; Anhydrotic Ectodermal Dysplasia, X Linked; CST Syndromes; Christ Siemens Touraine Syndrome; Dysplasia 1, Ectodermal; Ectodermal Dysplasia 1s; Syndrome, CST; Syndromes, CST; X Linked Hypohydridic Ectodermal Dysplasia; Christ-Siemens-Touraine Syndrome