Hyper-IgM Immunodeficiency Syndrome, Type 1
"Hyper-IgM Immunodeficiency Syndrome, Type 1" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An X-linked hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 LIGAND.
| Descriptor ID |
D053307
|
| MeSH Number(s) |
C15.378.147.333.249.500 C16.320.322.237 C20.673.430.249.500
|
| Concept/Terms |
Hyper-IgM Immunodeficiency Syndrome, Type 1- Hyper-IgM Immunodeficiency Syndrome, Type 1
- Hyper IgM Immunodeficiency Syndrome, Type 1
- Hyper-IgM Syndrome 1
- Hyper IgM Syndrome 1
- X-Linked Hyper IgM Syndrome
- X Linked Hyper IgM Syndrome
- Immunodeficiency with Hyper-IgM, Type 1
- Immunodeficiency with Hyper IgM, Type 1
- HIGM1
- HIGM1 Syndrome
- HIGM1 Syndromes
- Syndrome, HIGM1
- Syndromes, HIGM1
- Hyper-IgM Immunodeficiency, X-Linked
- Hyper IgM Immunodeficiency, X Linked
- Hyper-IgM Immunodeficiencies, X-Linked
- Immunodeficiencies, X-Linked Hyper-IgM
- Immunodeficiency, X-Linked Hyper-IgM
- X-Linked Hyper-IgM Immunodeficiencies
- X-Linked Hyper-IgM Immunodeficiency
|
Below are MeSH descriptors whose meaning is more general than "Hyper-IgM Immunodeficiency Syndrome, Type 1".
Below are MeSH descriptors whose meaning is more specific than "Hyper-IgM Immunodeficiency Syndrome, Type 1".
This graph shows the total number of publications written about "Hyper-IgM Immunodeficiency Syndrome, Type 1" by people in this website by year, and whether "Hyper-IgM Immunodeficiency Syndrome, Type 1" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hyper-IgM Immunodeficiency Syndrome, Type 1" by people in Profiles.
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50 Years Ago in The Journal of Pediatrics: Familial Granulocytopenia and Associated Immunoglobulin Abnormality: Report of 3 Cases in Young Brothers. J Pediatr. 2018 03; 194:39.
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X-linked hyper IgM syndrome: a novel sequence variant associated with an atypical mild phenotype. J Pediatr Hematol Oncol. 2012 Jul; 34(5):e212-4.