Structured Summary
Abstract
An autosomal dominant form of ectodermal dysplasia which is due to mutations in the gene for the EDAR RECEPTOR.
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Synonyms
2 entry terms
- Ectodermal Dysplasia 3, Anhidrotic
- Ectodermal Dysplasia, Hypohidrotic, Autosomal Dominant
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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 (1987-2006)
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References
- National Library of Medicine. Anhidrotic Ectodermal Dysplasia 3. Medical Subject Headings (MeSH). 2026. Unique ID D053359. http://id.nlm.nih.gov/mesh/2026/D053359
- Anhidrotic Ectodermal Dysplasia 3. In: Wikidata. https://www.wikidata.org/wiki/Q69277876