MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expand
liver disease (MONDO:0005154)
Parent Node:
expand
syndromic disease (MONDO:0002254)
..Starting node
..expand
hepatorenal syndrome ()

       Child Nodes:



 Sister Nodes: 
..expandAchard syndrome ()
..expandAchenbach syndrome ()
..expandacute chest syndrome ()
..expandacute coronary syndrome ()
..expandadult respiratory distress syndrome ()
..expandanterior spinal artery syndrome ()
..expandantiphospholipid syndrome ()
..expandautosomal dominant chondrodysplasia punctata ()
..expandBarre-Lieou syndrome ()
..expandbrachydactyly-nystagmus-cerebellar ataxia syndrome ()
..expandBrown-Sequard syndrome ()
..expandburning mouth syndrome ()
..expandCADASIL ()
..expandCapgras syndrome ()
..expandcapillary leak syndrome ()
..expandcarcinoid syndrome ()
..expandcauda equina syndrome ()
..expandcentral sleep apnea syndrome ()
..expandcleidocranial dysplasia ()
..expandcompartment syndrome ()
..expanddiffuse infiltrative lymphocytosis syndrome ()
..expanddry eye syndrome ()
..expandDuane retraction syndrome ()
..expanddumping syndrome ()
..expandempty sella syndrome ()
..expandeuthyroid sick syndrome ()
..expandFanconi syndrome ()
..expandFG syndrome ()
..expandfibrogenesis imperfecta ossium ()
..expandfibromyalgia ()
..expandFroelich syndrome ()
..expandFuchs' heterochromic uveitis ()
..expandGorham disease ()
..expandhepatorenal syndrome ()
..expandhypoplastic left heart syndrome ()
..expandinclusion body myopathy with Paget disease of bone and frontotemporal dementia ()
..expandirritable bowel syndrome ()
..expandKluver-Bucy syndrome ()
..expandlateral medullary syndrome ()
..expandlong QT syndrome ()
..expandLown-Ganong-Levine syndrome ()
..expandmedian arcuate ligament syndrome ()
..expandmetabolic syndrome ()
..expandmiliaria ()
..expandmultiple chemical sensitivity ()
..expandmyalgic encephalomeyelitis/chronic fatigue syndrome ()
..expandnephrotic syndrome ()
..expandobstructive sleep apnea syndrome ()
..expandpalindromic rheumatism ()
..expandPatau syndrome ()
..expandpersian gulf syndrome ()
..expandPotter syndrome ()
..expandReye syndrome ()
..expandsick sinus syndrome ()
..expandsubclavian steal syndrome ()
..expandsubstance withdrawal syndrome ()
..expandsuperior mesenteric artery syndrome ()
..expandsyndromic intellectual disability ()
..expandtarsal tunnel syndrome ()
..expandtethered spinal cord syndrome ()
..expandthoracic outlet syndrome ()
..expandTietze syndrome ()
..expandtoxic shock syndrome ()
..expandvertebral artery insufficiency ()
..expandWaterhouse-Friderichsen syndrome ()
..expandWissler syndrome ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:1382
Name:hepatorenal syndrome
Definition:Hepatorenal syndrome is a form of impaired kidney function that occurs in individuals with advanced chronic liver disease. As many as 40% of individuals with cirrhosis and ascites will develop hepatorenal syndrome. Symptoms may include fatigue, abdominal pain, and a general feeling of ill health ( malaise ). There are two distinct types of hepatorenal syndrome. Type I progresses quickly (within days), leading to kidney failure . Individuals with type I typically have dramatically reduced urine output, edema , and jaundice , and often suffer from hepatic encephalopathy . Type II progresses more slowly, over weeks or months, and the symptoms are less severe. The cause of hepatorenal syndrome is unknown. A contributing factor seems to be a narrowing of the blood vessels that connect into the kidneys. This causes a decrease in blood flow to the kidneys, impairing their function. In some cases, triggers or precipitating factors (infections, blood loss from the gastrointestinal tract, low blood pressure) are involved. Treatment is aimed at helping the liver work better and maintaining kidney function. In many cases, a liver transplant is needed. In some cases, individuals also need a kidney transplant .
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:hepato-renal syndrome
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal