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".
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