| Descriptor English: | Familial Mediterranean Fever | ||||||
| Descriptor Spanish: |
Fiebre Mediterránea Familiar
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| Descriptor Portuguese: | Febre Familiar do Mediterrâneo | ||||||
| Descriptor French: | Fièvre méditerranéenne familiale | ||||||
| Entry term(s): |
Benign Paroxysmal Peritonitides Benign Paroxysmal Peritonitis Disease, Periodic Disease, Wolff Periodic Disease, Wolff's Periodic Diseases, Periodic Familial Mediterranean Fever, Autosomal Dominant Familial Mediterranean Fever, Autosomal Recessive Familial Paroxysmal Polyserositides Familial Paroxysmal Polyserositis Mediterranean Fever, Familial Paroxysmal Peritonitides, Benign Paroxysmal Peritonitis, Benign Paroxysmal Polyserositides, Familial Paroxysmal Polyserositis, Familial Periodic Disease Periodic Disease, Wolff Periodic Disease, Wolff's Periodic Disease, Wolffs Periodic Diseases Periodic Peritonitides Periodic Peritonitis Peritonitides, Benign Paroxysmal Peritonitides, Periodic Peritonitis, Benign Paroxysmal Peritonitis, Periodic Polyserositides, Familial Paroxysmal Polyserositides, Recurrent Polyserositis, Familial Paroxysmal Polyserositis, Recurrent Recurrent Polyserositides Recurrent Polyserositis Wolff Periodic Disease Wolff's Periodic Disease Wolffs Periodic Disease |
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| Tree number(s): |
C16.320.382.625 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D010505 | ||||||
| Scope note: | 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. |
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| Annotation: | a specific disease entity: do not use entry term PERIODIC DISEASE for periodically occurring disease (= PERIODICITY (IM) + disease (IM)) |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 2000; see PERIODIC DISEASE 1966-1999; for FAMILIAL MEDITERRANEAN FEVER see PERIODIC DISEASE 1966-1999 |
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| History Note: | 2000 (1966) |
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| DeCS ID: | 10696 | ||||||
| Unique ID: | D010505 | ||||||
| NLM Classification: | WB 720 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2000/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2013/07/08 |
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Familial Mediterranean Fever
- Preferred
Familial Mediterranean Fever, Autosomal Dominant
- Related but not broader or narrower
| Concept UI |
M0016320 |
| Scope note | 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. |
| Preferred term | Familial Mediterranean Fever |
| Entry term(s) |
Benign Paroxysmal Peritonitides Benign Paroxysmal Peritonitis Disease, Periodic Disease, Wolff Periodic Disease, Wolff's Periodic Diseases, Periodic Familial Mediterranean Fever, Autosomal Recessive Familial Paroxysmal Polyserositides Familial Paroxysmal Polyserositis Mediterranean Fever, Familial Paroxysmal Peritonitides, Benign Paroxysmal Peritonitis, Benign Paroxysmal Polyserositides, Familial Paroxysmal Polyserositis, Familial Periodic Disease Periodic Disease, Wolff Periodic Disease, Wolff's Periodic Disease, Wolffs Periodic Diseases Periodic Peritonitides Periodic Peritonitis Peritonitides, Benign Paroxysmal Peritonitides, Periodic Peritonitis, Benign Paroxysmal Peritonitis, Periodic Polyserositides, Familial Paroxysmal Polyserositides, Recurrent Polyserositis, Familial Paroxysmal Polyserositis, Recurrent Recurrent Polyserositides Recurrent Polyserositis Wolff Periodic Disease Wolff's Periodic Disease Wolffs Periodic Disease |
| Concept UI |
M0565321 |
| Preferred term | Familial Mediterranean Fever, Autosomal Dominant |
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