Hypermethioninemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An amino acid metabolic disorder that involves an excess of the amino acid methionine, in the blood. This condition can occur when methionine is not broken down properly in the body. (Human Disease Ontology, DOID_0050544)
External Link https://www.disgenet.org/browser/0/1/0/C1847720
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Genes

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

Symbol Name
AHCY adenosylhomocysteinase
GNMT glycine N-methyltransferase
MAT1A methionine adenosyltransferase I, alpha