MeSH Browser

MeSH Supplementary: Agammaglobulinemia, non-Bruton type
Unique ID: C538056
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538056
Entry Term(s): Agammaglobulinemia due to early proB cell defect; Agammaglobulinemia, Non-Bruton Type, Autosomal Recessive; Agammaglobulinemia, autosomal recessive
Registry Numbers: 0
Heading Mapped to: *Agammaglobulinemia
Frequency: 11
Date of Entry: 2010/06/25
Revision Date: 2012/08/24

Agammaglobulinemia, non-Bruton type MeSH Supplementary Concept Data 2025