MeSH Browser

MeSH Supplementary: Bruton type agammaglobulinemia
Unique ID: C537409
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537409
Entry Term(s): Agammaglobulinemia, BTK; Agammaglobulinemia, Bruton tyrosine kinase; Agammaglobulinemia, X-Linked; Agammaglobulinemia, X-Linked, Type I; Bruton's Agammaglobulinemia; Bruton-Type Agammaglobulinemia; Bruton-type (congenital X-linked) agammaglobulinemia; Congenital Agammaglobulinemia; Immunodeficiency 1; X-linked agammaglobulinemia
Heading Mapped to: *Agammaglobulinemia; *Genetic Diseases, X-Linked
Frequency: 330
Note: A hereditary immunodeficiency due to the failure of B-LYMPHOCYTES to mature and rearrangement failure of IG HEAVY CHAINS. Mutations in Agammaglobulinaemia tyrosine kinase (BTK gene) can cause X-linked AGAMMAGLOBULINEMIA type 1 (XLA). OMIM: 300755
Date of Entry: 2010/08/25
Revision Date: 2015/08/17

Bruton type agammaglobulinemia MeSH Supplementary Concept Data 2024