Susceptibility to viral and mycobacterial infections due to STAT1 deficiency

Orpha code: 391311OMIM code: 613796

Definicja

A rare, genetic, primary immunodeficiency due to a defect in innate immunity disorder characterized by impaired intracellular signaling from both type I and type II interferons, leading to early-onset, severe, life-threatening intracellular bacterial (typically mycobacteria) and viral (mainly herpes viruses) infections.

Disease data
Klasyfikacja

Disease

Synonimy
Predisposition to severe viral infection due to STAT1 deficiency
STAT1 deficiency
Predisposition to severe viral infection due to STAT1 deficiency
STAT1 deficiency
Kod ORPHA
391311
Kod OMIM
613796
Kod ICD10
D84.8
Kod ICD11
-

No additional description.

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