ORPHA:342

Familial Mediterranean fever

Also called Benign paroxysmal peritonitis, Benign recurrent polyserositis, FMF, Familial paroxysmal polyserositis, Periodic disease

Body system

Immunological diseases

Inheritance pattern

Autosomal dominant, Autosomal recessive

Typical age of onset

Adolescent, Adult, Childhood, Infancy

Estimated prevalence

>1 / 1000 (Turkey)

Rarity class

>1 / 1000

ORPHA:342 is classified under "Immunological diseases" in the Orphanet nomenclature.