phenylalanine hydroxylase deficiency Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A reduction in phenylalanine 4-monooxygenase activity. (Human Phenotype Ontology, HP_0005982)
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Genes

1 genes associated with the disease phenylalanine hydroxylase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
PAH phenylalanine hydroxylase