decreased csf homovanillic acid (hva) Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Decreased concentration of homovanillic acid (HVA) in the cerebrospinal fluid. HVA is a metabolite of dopamine. (Human Phenotype Ontology, HP_0003785)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003785
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Genes

3 genes associated with the decreased csf homovanillic acid (hva) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DDC dopa decarboxylase (aromatic L-amino acid decarboxylase)
PNPO pyridoxamine 5'-phosphate oxidase
TH tyrosine hydroxylase