Hypogammaglobulinemia, X-Linked MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Hypogammaglobulinemia, X-Linked
Unique ID: C562478
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562478
Registry Numbers: 0
Heading Mapped to: *Agammaglobulinemia; *Genetic Diseases, X-Linked
Frequency: 3
Note: mutation in Bruton tyrosine kinase
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Hypogammaglobulinemia, X-Linked Preferred

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