respiratory alkalosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Alkalosis due to excess loss of carbon dioxide from the body. (Human Phenotype Ontology, HP_0001950)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001950
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Genes

5 genes associated with the respiratory alkalosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ASL argininosuccinate lyase
ASS1 argininosuccinate synthase 1
CA5A carbonic anhydrase VA, mitochondrial
CPS1 carbamoyl-phosphate synthase 1, mitochondrial
OTC ornithine carbamoyltransferase