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Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Ectodermal Dysplasia > Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Ectodermal Dysplasia > Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Abnormalities, Multiple > Ectodermal Dysplasia > Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
Skin and Connective Tissue Diseases > Skin Diseases > Skin Abnormalities > Ectodermal Dysplasia > Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Skin Abnormalities > Ectodermal Dysplasia > Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive

Preferred term

Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

  • Anhidridic Ectodermal Dysplasia, Autosomal Recessive
  • Anhidrotic Ectodermal Dysplasia, Autosomal Recessive
  • Anhydridic Ectodermal Dysplasia, Autosomal Recessive
  • Autosomal Recessive Anhidrotic Ectodermal Dysplasia
  • Autosomal Recessive Anhydrotic Ectodermal Dysplasia
  • Ectodermal Dysplasia, Anhidrotic, Autosomal Recessive
  • Ectodermal Dysplasia, Hypohydrotic, Autosomal Recessive

Scope note

  • An autosomal recessive form of ectodermal dysplasia which is due to mutations in the gene for the EDAR RECEPTOR or EDAR-ASSOCIATED DEATH DOMAIN PROTEIN.

History note

  • 2007

In other languages

URI

http://www.yso.fi/onto/mesh/D053360

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