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Hypogammaglobulinemia, X-Linked MeSH Supplementary Concept Data 2022


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