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.
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
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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Below are the most recent publications written about "Ectodermal Dysplasia 3, Anhidrotic" by people in Profiles.