hypermethioninemia Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
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)
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Genes

3 genes involed in the disease hypermethioninemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

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