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... > 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
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Genetic Diseases, X-Linked > Hyper-IgM Immunodeficiency Syndrome, Type 1

Preferred term

Hyper-IgM Immunodeficiency Syndrome, Type 1  

Type

  • mesh:Descriptor

Definition

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

Broader concept

Entry terms

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

Allowable Qualifier(s)

In other languages

  • Syndrome d'hyper-IgM lié à l'X

    French

  • HIGM1
  • Hyperimmunoglobulinémie M liée à l'X
  • Syndrome d'HIGM1
  • Syndrome d'hyper IgM de type 1
  • Syndrome d'hyper-IgM de type 1
  • Syndrome d'hyper-IgM de type I
  • Syndrome HIGM1

URI

http://data.loterre.fr/ark:/67375/JVR-XP0SKMMB-8

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RDF/XML TURTLE JSON-LD Created 7/5/06, last modified 6/17/19