MeSH Browser

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

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urine (UR)

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Ectodermal Dysplasia 1, Anhidrotic MeSH Descriptor Data 2025