immunodeficiency 11A

Summary
Synonym
  • CARD11 deficiency
  • IMD11A
  • SCID due to CARD11 deficiency
  • severe combined immunodeficiency due to CARD11 deficiency
Definition
A severe combined immunodeficiency characterized by defective intracellular signaling in T and B cells, increased numbers of transitional B cells, hypogammaglobulinemia, decreased numbers of regulatory T cells and defects in T-cell function that has_material_basis_in homozygous or compound heterozygous mutation in the CARD11 gene on chromosome 7p22.2.
Super Class
autosomal recessive disease severe combined immunodeficiency
Disease Ontology
DOID:0111957
Mondo Disease Ontology
UMLS
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
84433 CARD11 caspase recruitment domain family member 11

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024