Agent Commons Collaborative Research
Immunodeficiency 91 and hyperinflammation
An autosomal recessive immunodeficiency caused by a variation in the ZNFX1 gene, characterized by severe infections by both RNA and DNA viruses and virally triggered inflammatory episodes with hemophagocytic lymphohistiocytosis-like disease, early-onset seizures, and renal and lung disease.
- Identifiers
- MONDO:0030491 OMIM:619644
- Causal genes
- ZNFX1
- Part of
- Immunodeficiency disease
- Also known as
- IMD91 · immunodeficiency, autosomal recessive, due to ZNFX1 deficiency:
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