Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
"Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive" 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 recessive form of ectodermal dysplasia which is due to mutations in the gene for the EDAR RECEPTOR or EDAR-ASSOCIATED DEATH DOMAIN PROTEIN.
MeSH Number(s)
C16.131.077.350.348
C16.131.831.350.348
C16.320.850.250.348
C17.800.804.350.348
C17.800.827.250.348
Concept/Terms
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive- Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
- Anhidrotic Ectodermal Dysplasia, Autosomal Recessive
- Ectodermal Dysplasia, Hypohydrotic, Autosomal Recessive
- Autosomal Recessive Anhidrotic Ectodermal Dysplasia
- Autosomal Recessive Anhydrotic Ectodermal Dysplasia
- Ectodermal Dysplasia, Anhidrotic, Autosomal Recessive
- Anhidridic Ectodermal Dysplasia, Autosomal Recessive
- Anhydridic Ectodermal Dysplasia, Autosomal Recessive
Below are MeSH descriptors whose meaning is more general than "Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive".
- 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, Hypohidrotic, Autosomal Recessive [C16.131.077.350.348]
- Skin Abnormalities [C16.131.831]
- Ectodermal Dysplasia [C16.131.831.350]
- Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive [C16.131.831.350.348]
- Genetic Diseases, Inborn [C16.320]
- Skin Diseases, Genetic [C16.320.850]
- Ectodermal Dysplasia [C16.320.850.250]
- Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive [C16.320.850.250.348]
- Skin and Connective Tissue Diseases [C17]
- Skin Diseases [C17.800]
- Skin Abnormalities [C17.800.804]
- Ectodermal Dysplasia [C17.800.804.350]
- Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive [C17.800.804.350.348]
- Skin Diseases, Genetic [C17.800.827]
- Ectodermal Dysplasia [C17.800.827.250]
- Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive [C17.800.827.250.348]
Below are MeSH descriptors whose meaning is more specific than "Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive".
This graph shows the total number of publications written about "Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive" by people in Harvard Catalyst Profiles by year, and whether "Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive" was a major or minor topic of these publication.
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Below are the most recent publications written about "Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive" by people in Profiles.