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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.
推出的年份: 2000(1966)
副标题
树号: C16.320.382.625
MeSH 单一 ID: D010505
进入的组:
  • Polyserositis, Familial Paroxysmal
  • Familial Paroxysmal Polyserositides
  • Paroxysmal Polyserositides, Familial
  • Paroxysmal Polyserositis, Familial
  • Polyserositides, Familial Paroxysmal
  • Polyserositis, Recurrent
  • Polyserositides, Recurrent
  • Recurrent Polyserositides
  • Recurrent Polyserositis
  • Wolff Periodic Disease
  • Disease, Wolff Periodic
  • Periodic Disease, Wolff
  • Periodic Disease, Wolff's
  • Periodic Disease, Wolffs
  • Benign Paroxysmal Peritonitis
  • Benign Paroxysmal Peritonitides
  • Paroxysmal Peritonitides, Benign
  • Paroxysmal Peritonitis, Benign
  • Peritonitides, Benign Paroxysmal
  • Peritonitis, Benign Paroxysmal
  • Familial Mediterranean Fever, Autosomal Recessive
  • Familial Paroxysmal Polyserositis
  • Mediterranean Fever, Familial
  • Periodic Disease
  • Disease, Periodic
  • Diseases, Periodic
  • Periodic Diseases
  • Periodic Peritonitis
  • Periodic Peritonitides
  • Peritonitides, Periodic
  • Peritonitis, Periodic
  • Wolff's Periodic Disease
  • Disease, Wolff's Periodic
  • Wolffs Periodic Disease
  • Familial Mediterranean Fever, Autosomal Dominant

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