Structured Summary
Abstract
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.
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Synonyms
8 entry terms
- Anhidridic Ectodermal Dysplasia, Autosomal Recessive
- Anhidrotic Ectodermal Dysplasia, Autosomal Recessive
- Anhydridic Ectodermal Dysplasia, Autosomal Recessive
- Autosomal Recessive Anhidrotic Ectodermal Dysplasia
- Autosomal Recessive Anhydrotic Ectodermal Dysplasia
- Ectodermal Dysplasia, Anhidrotic, Autosomal Recessive
- Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
- Ectodermal Dysplasia, Hypohydrotic, Autosomal Recessive
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Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
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History Note
2007
MeSH Record
Previous Indexing
- Ectodermal Dysplasia (1971-2006)
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AMA Style
References
- National Library of Medicine. Hypohidrotic Autosomal Recessive Ectodermal Dysplasia. Medical Subject Headings (MeSH). 2026. Unique ID D053360. http://id.nlm.nih.gov/mesh/2026/D053360
- Hypohidrotic Autosomal Recessive Ectodermal Dysplasia. In: Wikidata. https://www.wikidata.org/wiki/Q54911667