ORPHA:574918

Predisposition to severe viral infection due to IRF7 deficiency

Body system

Immunological diseases

Inheritance pattern

Autosomal recessive

Typical age of onset

All ages

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:574918 is classified under "Immunological diseases" in the Orphanet nomenclature.