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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Genetic Diseases, X-Linked > Ectodermal Dysplasia 1, Anhidrotic
Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Ectodermal Dysplasia > Ectodermal Dysplasia 1, Anhidrotic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Ectodermal Dysplasia > Ectodermal Dysplasia 1, Anhidrotic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Skin Abnormalities > Ectodermal Dysplasia > Ectodermal Dysplasia 1, Anhidrotic
Skin and Connective Tissue Diseases > Skin Diseases > Skin Abnormalities > Ectodermal Dysplasia > Ectodermal Dysplasia 1, Anhidrotic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Abnormalities, Multiple > Ectodermal Dysplasia > Ectodermal Dysplasia 1, Anhidrotic

Preferred term

Ectodermal Dysplasia 1, Anhidrotic  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

  • Anhidrotic Ectodermal Dysplasia, X Linked
  • Anhidrotic Ectodermal Dysplasia, X-Linked
  • Anhydrotic Ectodermal Dysplasia, X Linked
  • Anhydrotic Ectodermal Dysplasia, X-Linked
  • Christ Siemens Touraine Syndrome
  • Christ-Siemens-Touraine Syndrome
  • CST Syndrome
  • CST Syndromes
  • Dysplasia 1, Ectodermal
  • Ectodermal Dysplasia 1
  • Ectodermal Dysplasia 1, Anhydrotic
  • Ectodermal Dysplasia 1s
  • Ectodermal Dysplasia, Anhidrotic, X-Linked
  • Ectodermal Dysplasia, Hypohidrotic, X-Linked
  • Ectodermal Dysplasia, Hypohydridic, X-Linked
  • Hypohidrotic Ectodermal Dysplasia
  • Syndrome, CST
  • Syndromes, CST
  • X Linked Hypohydridic Ectodermal Dysplasia
  • X-Linked Hypohydridic Ectodermal Dysplasia

Scope note

  • An X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ECTODYSPLASIN.

History note

  • 2007(1993)

In other languages

URI

http://www.yso.fi/onto/mesh/D053358

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