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Intermittent hydrarthrosis

2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Budd-Chiari syndrome

1 OMIM reference -
2 associated genes
20 signs/symptoms

Intermittent hydrarthrosis

Budd-Chiari syndrome

MEFV	(UniProt - OMIM)		F5	(UniProt - OMIM)
TNFRSF1A	(UniProt - OMIM)		JAK2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TNFRSF1A	(0.88)	JAK2

Citations in the biomedical literature:

Intermittent hydrarthrosis		Budd-Chiari syndrome

	Classification (Orphanet): - Rare genetic disease - Rare systemic or rheumatologic disease		Classification (Orphanet): - Rare hepatic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the circulatory system -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: variable Average age of death: any age Type of inheritance: multigenic/multifactorial

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D006502

Budd-Chiari syndrome
	Very frequent - Ascitis - Portal hypertension - Splenomegaly Frequent - Abnormal hepatic enzymes / transaminases - Acute abdominal pain / colic - Cirrhosis - Esophageal varices - Fever / chilling - Hepatocellular liver disease / hepatic failure - Hepatomegaly / liver enlargement (excluding storage disease) Occasional - Acute hepatic failure - Acute ischemic syndrome - Biliary / gallbladder stones / lithiasis / cholecystitis - Gastrointestinal bleeding / hemorrhage / hematemesis / melena / rectorrhagia - Hepatitis / icterus / cholestasis - Intestinal obstruction / ileus - Malabsorption / chronic diarrhea / steatorrhea - Mesenteric / intestinal infarction - Peritonitis / peritoneal abscess - Weight loss / loss of appetite / break in weight curve / general health alteration
Intermittent hydrarthrosis
(no data available)