ORPHA:200418

Immunodeficiency with factor I anomaly

Also called Complete factor I deficiency

Body system

Immunological diseases

Inheritance pattern

Autosomal recessive

Typical age of onset

Adolescent, Adult, Childhood

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:200418 is classified under "Immunological diseases" in the Orphanet nomenclature.