Agammaglobulinemia, Non-Bruton Type, Autosomal Dominant MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Agammaglobulinemia, Non-Bruton Type, Autosomal Dominant
Unique ID: C563305
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563305
Registry Numbers: 0
Heading Mapped to: *Agammaglobulinemia
Frequency: 0
Note: this form caused by mutation in mu immunoglobulin heavy-chain gene
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Agammaglobulinemia, Non-Bruton Type, Autosomal Dominant Preferred

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