low plasma citrulline Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A decreased concentration of citrulline in the blood. (Human Phenotype Ontology, HP_0003572)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003572
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Genes

2 genes associated with the low plasma citrulline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CPS1 carbamoyl-phosphate synthase 1, mitochondrial
OTC ornithine carbamoyltransferase