Structured Summary
Abstract
A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposition to a lowered threshold for pruritus. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. In infants it is known as infantile eczema.
MeSH Record
Classification
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MeSH Record
Synonyms
9 entry terms
- Dermatitis, Atopic
- Eczema, Atopic
- Neurodermatitis, Atopic
- Neurodermatitis, Disseminated
- Atopic Eczema
- Atopic Neurodermatitis
- Disseminated Neurodermatitis
- Eczema, Infantile
- Infantile Eczema
MeSH Record
Aspects Covered
35 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, 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.
MeSH Record
Indexing Annotation
a type of immediate hypersensitivity
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MeSH Record
NLM Classification
WR 160
AMA Style
References
- National Library of Medicine. Atopic Dermatitis. Medical Subject Headings (MeSH). 2026. Unique ID D003876. http://id.nlm.nih.gov/mesh/2026/D003876
- Atopic Dermatitis. In: Wikipedia. https://en.wikipedia.org/wiki/Atopic_dermatitis
- Atopic Dermatitis. In: Wikidata. https://www.wikidata.org/wiki/Q268667