Agent Commons Collaborative Research
Immunodeficiency 92
rareAn autosomal recessive primary immunodeficiency characterized by the onset of recurrent infections in infancy or early childhood. Infectious agents are broad, including bacterial, viral, fungal, and parasitic, including Cryptosporidium and Mycobacteria. Patient lymphocytes show defects in both T- and B-cell proliferation, cytokine secretion, and overall function, and there is also evidence of dysfunction of NK, certain antigen-presenting cells, and myeloid subsets. Hematopoietic stem cell transplantation may be curative.
- Identifiers
- MONDO:0030498 OMIM:619652Orphanet:697394
- Causal genes
- REL
- Part of
- Immunodeficiency disease
- Also known as
- IMD92 · immunodeficiency due to REL deficiency
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