ORPHA:2966

Properdin deficiency

Body system

Immunological diseases

Inheritance pattern

X-linked recessive

Typical age of onset

Adolescent, Adult, Childhood, Infancy

Estimated prevalence

1-9 / 1 000 000 (Worldwide)

Rarity class

1-9 / 1 000 000

ORPHA:2966 is classified under "Immunological diseases" in the Orphanet nomenclature.