fulminant hepatic failure Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004448
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Genes

3 genes associated with the fulminant hepatic failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GFM1 G elongation factor, mitochondrial 1
HADH hydroxyacyl-CoA dehydrogenase
SH2D1A SH2 domain containing 1A