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Familial Mediterranean fever

MONDO:0018088

Familial Mediterranean fever (FMF) is an autoinflammatory disorder characterized by recurrent short episodes of fever and serositis resulting in pain in the abdomen, chest, joints and muscles.

Also known as: FMF, Fiebre mediterránea familiar, benign paroxysmal peritonitis, benign recurrent polyserositis, familial paroxysmal polyserositis, periodic disease

59 clinical trials for this condition and its sub-types.

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Sub-types

Autosomal recessive familial Mediterranean fever (0) Familial Mediterranean fever, autosomal dominant (0)

Broader categories

Disease (618) Hereditary disease (172) Immune system disorder (140) Rheumatic disorder (80) Connective tissue disorder (67) Syndromic disease (24) Autoinflammatory syndrome (18) Human disease (14) Hereditary periodic fever syndrome (5) Disease of genetic or genomic mechanism (2)

Trials to join now! 27 Not yet recruiting 7 Not yet finished but already full! 8 Completed 17