Familial Mediterranean Fever (FMF)

Familial Mediterranean Fever(来自ICD-11)

别称:

Benign Paroxysmal Peritonitis

Periodic Disease

Fmf

Familial Paroxysmal Polyserositis

Familial Mediterranean Fever, Autosomal Recessive

Familial Mediterranean Fever, Ar

Benign Recurrent Polyserositis

Recurrent Polyserositis

Periodic Fever

Fever, Mediterranean, Familial, Autosomal Recessive

Autosomal Recessive Familial Mediterranean Fever

Hereditary Autoinflammatory Diseases

Fmf - [familial Mediterranean Fever]

Familial Non-Neuropathic Amyloidosis

Polyserositis, Familial Paroxysmal

Familial Recurrent Polyserositis

Periodic Familial Polyserositis

Hereditary Amyloid Nephropathy

Mediterranean Fever, Familial

Periodic Familial Peritonitis

Siegal-Cattan-Mamou Disease

Siegal Cattan Mamou Disease

Polyserositis, Recurrent

Reimann Periodic Disease

Paroxysmal Polyserositis

Riemann Periodic Disease

Periodic Fever Syndrome

Wolff Periodic Disease

Periodic Polyserositis

Armenian Disease

Arfmf

Mef

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Familial Mediterranean Fever, also known as benign paroxysmal peritonitis, is related to familial mediterranean fever, autosomal dominant and brucellosis, and has symptoms including abdominal pain, arthralgia and fever. An important gene associated with Familial Mediterranean Fever is MEFV (MEFV Innate Immunity Regulator, Pyrin), and among its related pathways/superpathways are Infectious disease and Innate Immune System. The drugs Tubulin Modulators and Antirheumatic Agents have been mentioned in the context of this disorder. Affiliated tissues include spinal cord and kidney, and related phenotypes are nausea and vomiting and constipation

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