Ectodermal Dysplasia 1, Anhidrotic
An X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ECTODYSPLASIN.
Year introduced: 2007(1993)
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Subheadings:
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
MeSH Unique ID: D053358
Entry Terms:
- X-Linked Hypohydridic Ectodermal Dysplasia
- X Linked Hypohydridic Ectodermal Dysplasia
- Ectodermal Dysplasia 1
- Dysplasia 1, Ectodermal
- Ectodermal Dysplasia 1s
- Ectodermal Dysplasia, Anhidrotic, X-Linked
- Ectodermal Dysplasia, Hypohidrotic, X-Linked
- Hypohidrotic Ectodermal Dysplasia
- CST Syndrome
- CST Syndromes
- Syndrome, CST
- Syndromes, CST
- Christ-Siemens-Touraine Syndrome
- Christ Siemens Touraine Syndrome
- Ectodermal Dysplasia, Hypohydridic, X-Linked
- Anhidrotic Ectodermal Dysplasia, X-Linked
- Anhidrotic Ectodermal Dysplasia, X Linked
- Anhydrotic Ectodermal Dysplasia, X-Linked
- Anhydrotic Ectodermal Dysplasia, X Linked
- Ectodermal Dysplasia 1, Anhydrotic
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