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.

Also known as: IMD91, immunodeficiency, autosomal recessive, due to ZNFX1 deficiency:

0 clinical trials for this condition and its sub-types, 0 tagged with Immunodeficiency 91 and hyperinflammation itself.