Familial Mediterranean Fever

A group of HEREDITARY AUTOINFLAMMATION DISEASES, characterized by recurrent fever, abdominal pain, headache, rash, PLEURISY; and ARTHRITIS. ORCHITIS; benign MENINGITIS; and AMYLOIDOSIS may also occur. Homozygous or compound heterozygous mutations in marenostrin gene encoding PYRIN result in autosomal recessive transmission; simple heterozygous, autosomal dominant form of the disease also exists with mutations in the same gene.

Also Known As:

Periodic Disease; Mediterranean Fever, Familial; Wolff Periodic Disease; Benign Paroxysmal Peritonitis; Familial Mediterranean Fever, Autosomal Dominant; Familial Mediterranean Fever, Autosomal Recessive; Familial Paroxysmal Polyserositis; Periodic Peritonitis; Polyserositis, Familial Paroxysmal; Polyserositis, Recurrent; Recurrent Polyserositis; Benign Paroxysmal Peritonitides; Disease, Periodic; Disease, Wolff Periodic; Disease, Wolff's Periodic; Diseases, Periodic; Familial Paroxysmal Polyserositides; Paroxysmal Peritonitides, Benign; Paroxysmal Peritonitis, Benign; Paroxysmal Polyserositides, Familial; Paroxysmal Polyserositis, Familial; Periodic Disease, Wolff; Periodic Disease, Wolffs; Periodic Diseases; Periodic Peritonitides; Peritonitides, Benign Paroxysmal; Peritonitides, Periodic; Peritonitis, Benign Paroxysmal; Peritonitis, Periodic; Polyserositides, Familial Paroxysmal; Polyserositides, Recurrent; Recurrent Polyserositides; Wolffs Periodic Disease; Periodic Disease, Wolff's; Wolff's Periodic Disease

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Hereditary Autoinflammatory Diseases: 43
    - Familial Mediterranean Fever: 1604

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Disease

Drug/Important Bio-Agent (IBA)