hyperoxaluria Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increased excretion of oxalates in the urine. (Human Phenotype Ontology, HP_0003159)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003159
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Genes

4 genes associated with the hyperoxaluria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGXT alanine-glyoxylate aminotransferase
GRHPR glyoxylate reductase/hydroxypyruvate reductase
HOGA1 4-hydroxy-2-oxoglutarate aldolase 1
PEX1 peroxisomal biogenesis factor 1