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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Genetic Diseases, X-Linked > Hyper-IgM Immunodeficiency Syndrome, Type 1
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Protein Disorders > Dysgammaglobulinemia > Hyper-IgM Immunodeficiency Syndrome > Hyper-IgM Immunodeficiency Syndrome, Type 1
Immune System Diseases > Immunologic Deficiency Syndromes > Dysgammaglobulinemia > Hyper-IgM Immunodeficiency Syndrome > Hyper-IgM Immunodeficiency Syndrome, Type 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Primary Immunodeficiency Diseases > Hyper-IgM Immunodeficiency Syndrome > Hyper-IgM Immunodeficiency Syndrome, Type 1
Immune System Diseases > Immunologic Deficiency Syndromes > Primary Immunodeficiency Diseases > Hyper-IgM Immunodeficiency Syndrome > Hyper-IgM Immunodeficiency Syndrome, Type 1

Preferred term

Hyper-IgM Immunodeficiency Syndrome, Type 1  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • HIGM1
  • HIGM1 Syndrome
  • HIGM1 Syndromes
  • Hyper-IgM Immunodeficiencies, X-Linked
  • Hyper IgM Immunodeficiency, X Linked
  • Hyper-IgM Immunodeficiency, X-Linked
  • Hyper IgM Syndrome 1
  • Hyper-IgM Syndrome 1
  • Immunodeficiencies, X-Linked Hyper-IgM
  • Immunodeficiency with Hyper IgM, Type 1
  • Immunodeficiency with Hyper-IgM, Type 1
  • Immunodeficiency, X-Linked Hyper-IgM
  • X-Linked Hyper-IgM Immunodeficiencies
  • X-Linked Hyper-IgM Immunodeficiency
  • X Linked Hyper IgM Syndrome
  • X-Linked Hyper IgM Syndrome

Scope note

  • An X-linked hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 LIGAND.

History note

  • 2007

In other languages

URI

http://www.yso.fi/onto/mesh/D053307

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