|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Hepatic failure refers to the inability of the liver to perform its normal synthetic and metabolic functions, which can result in coagulopathy and alteration in the mental status of a previously healthy individual. Hepatic failure is defined as fulminant if there is onset of encephalopathy within 4 weeks of the onset of symptoms in a patient with a previously healthy liver. (Human Phenotype Ontology, HP_0004448)|
|Downloads & Tools|
3 genes associated with the fulminant hepatic failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.