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Ectodermal Dysplasia 1, Anhidrotic MeSH Descriptor Data 2021


MeSH Heading
Ectodermal Dysplasia 1, Anhidrotic
Tree Number(s)
C16.131.077.350.198
C16.131.831.350.198
C16.320.322.116
C16.320.850.250.198
C17.800.804.350.198
C17.800.827.250.198
Unique ID
D053358
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D053358
Scope Note
An X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ECTODYSPLASIN.
Entry Term(s)
Anhidrotic Ectodermal Dysplasia, X-Linked
Anhydrotic Ectodermal Dysplasia, X-Linked
CST Syndrome
Christ-Siemens-Touraine 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
See Also
Ectodysplasins
Public MeSH Note
2007; see ECTODERMAL DYSPLASIA 1993-2006
History Note
2007(1993)
Date Established
2007/01/01
Date of Entry
2006/07/05
Revision Date
2015/06/18
Ectodermal Dysplasia 1, Anhidrotic Preferred
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