 Ectodermal Dysplasia 3, Anhidrotic
"Ectodermal Dysplasia 3, 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 autosomal dominant form of ectodermal dysplasia which is due to mutations in the gene for the EDAR RECEPTOR.
| Descriptor ID |
D053359
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| MeSH Number(s) |
C16.131.077.350.298 C16.131.831.350.298 C16.320.850.250.298 C17.800.804.350.298 C17.800.827.250.298
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Ectodermal Dysplasia 3, 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 3, Anhidrotic [C16.131.077.350.298]
- Skin Abnormalities [C16.131.831]
- Ectodermal Dysplasia [C16.131.831.350]
- Ectodermal Dysplasia 3, Anhidrotic [C16.131.831.350.298]
- Genetic Diseases, Inborn [C16.320]
- Skin Diseases, Genetic [C16.320.850]
- Ectodermal Dysplasia [C16.320.850.250]
- Ectodermal Dysplasia 3, Anhidrotic [C16.320.850.250.298]
- Skin and Connective Tissue Diseases [C17]
- Skin Diseases [C17.800]
- Skin Abnormalities [C17.800.804]
- Ectodermal Dysplasia [C17.800.804.350]
- Ectodermal Dysplasia 3, Anhidrotic [C17.800.804.350.298]
- Skin Diseases, Genetic [C17.800.827]
- Ectodermal Dysplasia [C17.800.827.250]
- Ectodermal Dysplasia 3, Anhidrotic [C17.800.827.250.298]
Below are MeSH descriptors whose meaning is more specific than "Ectodermal Dysplasia 3, Anhidrotic".
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