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".
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