Hypoammonemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A decreased concentration of ammonia in the blood. (Human Phenotype Ontology, HP_0100493)
External Link https://www.disgenet.org/browser/0/1/0/C4022041
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Genes

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

Symbol Name
OCRL oculocerebrorenal syndrome of Lowe