Structured Summary
Abstract
A clinically and genetically heterogeneous group of mast cell disorders in which there is aberrant release of mast cell mediators with little to no accompanying proliferation of MAST CELLS.
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Synonyms
9 entry terms
- Idiopathic Mast Cell Activation Disorder
- Mast Cell Activation Syndromes
- Non-Clonal Mast Cell Activation Disorder
- Non-Clonal Mast Cell Activation Syndrome
- Nonclonal Mast Cell Activation Syndrome
- nc-MCAS
- Non Clonal Mast Cell Activation Disorder
- Non Clonal Mast Cell Activation Syndrome
- nc MCAS
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
History Note
2022; for MAST CELL ACTIVATION SYNDROME use MASTOCYTOSIS 2018-2021
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AMA Style
References
- National Library of Medicine. Mast Cell Activation Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D000090267. http://id.nlm.nih.gov/mesh/2026/D000090267
- Mast Cell Activation Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/Mast_cell_activation_syndrome
- Mast Cell Activation Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q24238949