ORPHA:528623

Hereditary angioedema with C1Inh deficiency

Also called HAE with C1 inhibitor deficiency, HAE with C1Inh deficiency, Hereditary angioneurotic edema with C1 inhibitor deficiency, Hereditary angioneurotic edema with C1Inh deficiency

Body system

Immunological diseases

Inheritance pattern

Not applicable

Typical age of onset

Adult, Elderly

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:528623 is classified under "Immunological diseases" in the Orphanet nomenclature.