Ectodermal Dysplasia 1, Anhidrotic
"Ectodermal Dysplasia 1, Anhidrotic" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ECTODYSPLASIN.
| Descriptor ID |
D053358
|
| MeSH 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
|
| Concept/Terms |
Ectodermal Dysplasia 1, Anhidrotic- Ectodermal Dysplasia 1, Anhidrotic
- Ectodermal Dysplasia, Hypohydridic, X-Linked
- Anhidrotic Ectodermal Dysplasia, X-Linked
- Anhidrotic Ectodermal Dysplasia, X Linked
- Ectodermal Dysplasia 1, Anhydrotic
- CST Syndrome
- CST Syndromes
- Syndrome, CST
- Syndromes, CST
- 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
- Christ-Siemens-Touraine Syndrome
- Christ Siemens Touraine Syndrome
- Anhydrotic Ectodermal Dysplasia, X-Linked
- Anhydrotic Ectodermal Dysplasia, X Linked
|
Below are MeSH descriptors whose meaning is more general than "Ectodermal Dysplasia 1, Anhidrotic".
- Diseases [C]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Congenital Abnormalities [C16.131]
- Abnormalities, Multiple [C16.131.077]
- Ectodermal Dysplasia [C16.131.077.350]
- Ectodermal Dysplasia 1, Anhidrotic [C16.131.077.350.198]
- Skin Abnormalities [C16.131.831]
- Ectodermal Dysplasia [C16.131.831.350]
- Ectodermal Dysplasia 1, Anhidrotic [C16.131.831.350.198]
- Genetic Diseases, Inborn [C16.320]
- Genetic Diseases, X-Linked [C16.320.322]
- Ectodermal Dysplasia 1, Anhidrotic [C16.320.322.116]
- Skin Diseases, Genetic [C16.320.850]
- Ectodermal Dysplasia [C16.320.850.250]
- Ectodermal Dysplasia 1, Anhidrotic [C16.320.850.250.198]
- Skin and Connective Tissue Diseases [C17]
- Skin Diseases [C17.800]
- Skin Abnormalities [C17.800.804]
- Ectodermal Dysplasia [C17.800.804.350]
- Ectodermal Dysplasia 1, Anhidrotic [C17.800.804.350.198]
- Skin Diseases, Genetic [C17.800.827]
- Ectodermal Dysplasia [C17.800.827.250]
- Ectodermal Dysplasia 1, Anhidrotic [C17.800.827.250.198]
Below are MeSH descriptors whose meaning is more specific than "Ectodermal Dysplasia 1, Anhidrotic".
This graph shows the total number of publications written about "Ectodermal Dysplasia 1, Anhidrotic" by people in this website by year, and whether "Ectodermal Dysplasia 1, Anhidrotic" was a major or minor topic of these publications.
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Below are the most recent publications written about "Ectodermal Dysplasia 1, Anhidrotic" by people in Profiles.
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Twin boys with abnormal facies, atopy, and reduced ability to sweat. Pediatr Ann. 2007 Mar; 36(3):140-2.