familial mediterranean fever

Preferred Label : familial mediterranean fever;

MeSH definition : 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 result in autosomal recessive transmission; simple heterozygous, autosomal dominant form of the disease.; 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.;

MeSH synonym : periodic disease; diseases, periodic; periodic diseases; wolffs periodic disease; mediterranean fever, familial; periodic disease, wolff's; disease, wolff's periodic; periodic disease, wolffs; disease, periodic; disease, wolff periodic; periodic disease, wolff; wolff's periodic disease; wolff periodic disease; periodic peritonitis; periodic peritonitides; peritonitides, periodic; peritonitis, periodic; benign paroxysmal peritonitis; benign paroxysmal peritonitides; paroxysmal peritonitides, benign; paroxysmal peritonitis, benign; peritonitides, benign paroxysmal; peritonitis, benign paroxysmal; familial paroxysmal polyserositis; familial paroxysmal polyserositides; paroxysmal polyserositides, familial; paroxysmal polyserositis, familial; polyserositides, familial paroxysmal; polyserositis, familial paroxysmal; recurrent polyserositis; polyserositides, recurrent; polyserositis, recurrent; recurrent polyserositides;

CISMeF synonym : periodic fever syndromes, hereditary; fever, familial mediterranean; familial mediterranean fever, autosomal recessive;

MeSH annotation : a specific disease entity: do not use entry term PERIODIC DISEASE for periodically occurring disease ( PERIODICITY (IM) disease (IM));

Wikipedia link : https://en.wikipedia.org/wiki/Familial Mediterranean fever;

Details

Origin ID

D010505;

UMLS CUI

C0031069;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Congestive Heart Failure [NCIt concept]
- Familial recurrent polyserositis [MedDRA LLT]
- Hepatorenal syndrome [ICD-11 Subcategory]
- Non-neuropathic heredofamilial amyloidosis [ICD-10 Sub-category]
- Non-neuropathic heredofamilial amyloidosis [ICD-10 Sub-category (who)]
- periodic disease [TUV Concept]
Currated CISMeF NLP mapping
- Familial Mediterranean Fever [NCIt concept]
- Familial Mediterranean fever [ICD-11 Subcategory]
- Familial Mediterranean fever [ICD-9 code]
- Familial Mediterranean fever [ORDO Disease]
- Familial Mediterranean fever (disorder) [SNOMED CT concept]
- Familial mediterranean fever [MedDRA Preferred Term]
- Familial mediterranean fever [OMIM Phenotype]
- Familial recurrent polyseritis [PASCAL descriptor]
- Hereditary periodic fever (disorder) [SNOMED CT concept]
- Hereditary periodic fever syndrome [ORDO Disease]
- Periodic fever [MedDRA LLT]
- familial Mediterranean fever [DO Concept]
- familial mediterranean fever [Disease (Nov.)]
- hereditary periodic fever syndrome [Disease (Nov.)]
- periodic disease [SNOMED Notion]
DO Cross reference
- familial Mediterranean fever [DO Concept]
Manual NTBT mappings (CISMeF)
- Blau syndrome [ORDO Disease]
- CINCA syndrome [ORDO Disease]
- Granulomatous arthritis of childhood [ORDO Disease]
- Juvenile chronic recurrent multifocal osteomyelitis [ORDO Disease]
- Majeed syndrome [ORDO Disease]
- Periodic fever syndrome [ORDO Disease]
- Primary immunodeficiency due to a defect in innate immunity [ORDO Disease]
- Pyogenic arthritis-pyoderma gangrenosum-acne syndrome [ORDO Disease]
- Rare systemic disease [ORDO Disease]
- Sterile multifocal osteomyelitis with periostitis and pustulosis [ORDO Disease]
- Tumor necrosis factor receptor 1 associated periodic syndrome [ORDO Disease]
Ne pas confondre avec
- periodicity [MeSH Descriptor]
ORDO relation(s)
- Familial Mediterranean fever [ORDO Disease]
Record concept(s)
- Familial Mediterranean Fever, Autosomal Recessive [MeSH concept]
- familial mediterranean fever [MeSH concept]
- familial mediterranean fever, autosomal dominant [MeSH concept]
See also (suggested by CISMeF)
- fever [MeSH Descriptor]
- relapsing fever [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial Mediterranean Fever [NCIt concept]
- Familial Mediterranean fever [ICD-9 code]
- Familial Mediterranean fever (disorder) [SNOMED CT concept]
- Familial mediterranean fever [OMIM Phenotype]
- Familial mediterranean fever [MedDRA Preferred Term]
- Familial recurrent polyserositis [MedDRA LLT]
- familial Mediterranean fever [DO Concept]
- familial mediterranean fever [Disease (Nov.)]
- periodic disease [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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