ORPHA:331190

Immunodeficiency due to ficolin3 deficiency

Body system

Immunological diseases

Inheritance pattern

Autosomal recessive

Typical age of onset

Childhood

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:331190 is classified under "Immunological diseases" in the Orphanet nomenclature.