immunodeficiency 41

Summary
Synonym
  • CD25 deficiency
  • IL2RA deficiency
  • IMD41
  • immunodeficiency 41 with lymphoproliferation and autoimmunity
  • immunodeficiency due to CD25 deficiency
  • interleukin-2 receptor alpha chain deficiency
Definition
A combined immunodeficiency characterized by a defect in T cell regulation with proliferation of CD8+ T cells, impaired antibody specific responses, and elevated cytokines resulting in recurrent viral, fungal, and bacterial infections, lymphadenopathy, and variable autoimmune features that has_material_basis_in homozygous or compound heterozygous mutation in the IL2RA gene on chromosome 10p15.1.
Super Class
autosomal recessive disease combined immunodeficiency
Disease Ontology
DOID:0111968
Mondo Disease Ontology
MeSH
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
3559 IL2RA interleukin 2 receptor subunit alpha
Displaying 1 entry
Gene ID Gene Symbol Description Source
16184 Il2ra interleukin 2 receptor, alpha chain
Displaying 1 entry
Gene ID Gene Symbol Description Source
25704 Il2ra interleukin 2 receptor subunit alpha

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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