Hyper-IgM Immunodeficiency Syndrome, Type 1

History

Walker, Jacob

Morton, John

Westheimer, Bryce

Human motor unit recor

Hyper-IgM Immunodefici

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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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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".

Diseases [C]
Hemic and Lymphatic Diseases [C15]
Hematologic Diseases [C15.378]
Blood Protein Disorders [C15.378.147]
Dysgammaglobulinemia [C15.378.147.333]
Hyper-IgM Immunodeficiency Syndrome [C15.378.147.333.249]
Hyper-IgM Immunodeficiency Syndrome, Type 1 [C15.378.147.333.249.500]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Genetic Diseases, X-Linked [C16.320.322]
Hyper-IgM Immunodeficiency Syndrome, Type 1 [C16.320.322.237]
Immune System Diseases [C20]
Immunologic Deficiency Syndromes [C20.673]
Dysgammaglobulinemia [C20.673.430]
Hyper-IgM Immunodeficiency Syndrome [C20.673.430.249]
Hyper-IgM Immunodeficiency Syndrome, Type 1 [C20.673.430.249.500]

Below are MeSH descriptors whose meaning is related to "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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