Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Ectodermal Dysplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Skin Abnormalities
Ectodermal Dysplasia
Preferred term
Ectodermal Dysplasia 1, Anhidrotic
Type
-
Topical Descriptor
Broader concept
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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