chronic hepatic failure Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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8 genes associated with the chronic hepatic failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AKR1D1 aldo-keto reductase family 1, member D1
ALMS1 Alstrom syndrome protein 1
CC2D2A coiled-coil and C2 domain containing 2A
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3
GALT galactose-1-phosphate uridylyltransferase
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
TMEM67 transmembrane protein 67