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Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Ectodermal Dysplasia > Ectodermal Dysplasia 3, Anhidrotic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Ectodermal Dysplasia > Ectodermal Dysplasia 3, Anhidrotic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Skin Abnormalities > Ectodermal Dysplasia > Ectodermal Dysplasia 3, Anhidrotic
Skin and Connective Tissue Diseases > Skin Diseases > Skin Abnormalities > Ectodermal Dysplasia > Ectodermal Dysplasia 3, Anhidrotic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Abnormalities, Multiple > Ectodermal Dysplasia > Ectodermal Dysplasia 3, Anhidrotic

Preferred term

Ectodermal Dysplasia 3, Anhidrotic  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

  • Ectodermal Dysplasia, Hypohidrotic, Autosomal Dominant

Scope note

  • An autosomal dominant form of ectodermal dysplasia which is due to mutations in the gene for the EDAR RECEPTOR.

History note

  • 2007

In other languages

URI

http://www.yso.fi/onto/mesh/D053359

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