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Intermittent hydrarthrosis
2 associated genes
No signs/symptoms info
COMMON GENES: 1
Familial Mediterranean fever
2 OMIM references -
1 associated gene
39 signs/symptoms
Intermittent hydrarthrosis
Familial Mediterranean fever

MEFV
(UniProt - OMIM)
 MEFV
(UniProt - OMIM)
TNFRSF1A
(UniProt - OMIM)

COMMON
GENES 		MEFV


Citations in the biomedical literature:


Intermittent hydrarthrosis
MEFV TNFRSF1A
Familial Mediterranean fever



Intermittent hydrarthrosis
Familial Mediterranean fever

Synonym(s):
(no synonyms)

Synonym(s):
- Benign paroxysmal peritonitis
- Benign recurrent polyserositis
- FMF
- Familial paroxysmal polyserositis
- Periodic disease
Classification (Orphanet):
- Rare genetic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
- Rare renal disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
External references:
2 OMIM references -
1 MeSH reference: D010505
Familial Mediterranean fever

Very frequent
- Acute abdominal pain / colic
- Articular / joint pain / arthralgia
- Autosomal recessive inheritance
- Constipation
- Fever / chilling
- Myalgia / muscular pain
- Nausea / vomiting / regurgitation / merycism / hyperemesis

Frequent
- Abnormal pleura / hydrothorax / pleuresia / pleural effusion / chylothorax
- Acute diarrhea
- Arthritis / synovitis / synovial proliferation
- Enanthema / aphtosa / aphta / leukoplakia
- Erysipela
- Erythema / erythematous lesions / erythroderma / polymorphous erythema
- Proteinuria
- Seizures / epilepsy / absences / spasms / status epilepticus
- Thoracic / chest pain

Occasional
- Acute hepatic failure
- Acute ischemic syndrome
- Angor pectoris / myocardial infarction
- Ascitis
- Biological inflammatory syndrome / increased erythrocyte sedimentation rate / CRP
- Cardiac rhythm disorder / arrhythmia
- Cutaneous rash
- Edema of the legs / lower limbs
- Intestinal obstruction / ileus
- Lymphadenopathy / polyadenopathies
- Malabsorption / chronic diarrhea / steatorrhea
- Meningitis / meningeal syndrome
- Mesenteric / intestinal infarction
- Motor deficit / trouble
- Nephrotic syndrome
- Osteoarthritis
- Pancreatitis
- Pericardium anomalies / pericarditis / absence / cysts / pericardial effusion
- Renal disease / nephropathy
- Renal / kidney calcifications / nephrocalcinosis
- Splenomegaly
- Testes inflammation / orchitis
- Vascularitis / vasculitides / arteritis


Intermittent hydrarthrosis

(no data available)