Structured Summary
Abstract
An X-linked hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 LIGAND.
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Classification
Broader headings
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MeSH Record
Synonyms
18 entry terms
- HIGM1
- HIGM1 Syndrome
- Hyper-IgM Immunodeficiency Syndrome, Type 1
- Hyper-IgM Immunodeficiency, X-Linked
- Hyper-IgM Syndrome 1
- Immunodeficiency with Hyper-IgM, Type 1
- X-Linked Hyper IgM Syndrome
- HIGM1 Syndromes
- Hyper IgM Immunodeficiency Syndrome, Type 1
- Hyper IgM Immunodeficiency, X Linked
- Hyper IgM Syndrome 1
- Hyper-IgM Immunodeficiencies, X-Linked
- Immunodeficiencies, X-Linked Hyper-IgM
- Immunodeficiency with Hyper IgM, Type 1
- Immunodeficiency, X-Linked Hyper-IgM
- X Linked Hyper IgM Syndrome
- X-Linked Hyper-IgM Immunodeficiencies
- X-Linked Hyper-IgM Immunodeficiency
MeSH Record
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.
MeSH Record
History Note
2007
MeSH Record
Previous Indexing
- CD40 Ligand (2000-2006)
- Immunologic Deficiency Syndromes (1995-2006)
MeSH Hierarchy
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AMA Style
References
- National Library of Medicine. Type 1 Hyper-IgM Immunodeficiency Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D053307. http://id.nlm.nih.gov/mesh/2026/D053307
- Type 1 Hyper-IgM Immunodeficiency Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q54945742