Hyperphenylalaninemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An increased concentration of L-phenylalanine in the blood. (Human Phenotype Ontology, HP_0004923)
External Link https://www.disgenet.org/browser/0/1/0/C4017280
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Genes

2 genes associated with the disease Hyperphenylalaninemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
DNAJC12 DnaJ (Hsp40) homolog, subfamily C, member 12
PTS 6-pyruvoyltetrahydropterin synthase