Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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 http://www.omim.org/entry/613752
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Genes

1 genes associated with the Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
AHCY adenosylhomocysteinase