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methionine adenosyltransferase deficiency

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Hypermethioninemia due to methionine adenosyltransferase deficiency is a very rare metabolic disorder resulting in isolated hepatic hypermethioninemia that is usually benign due to partial inactivation of enzyme activity. Rarely patients have been found to have an odd odor or neurological disorders such as brain demyelination.
Uniprot Description An inborn error of metabolism resulting in isolated hypermethioninemia. Most patients have no clinical abnormalities, although some neurologic symptoms may be present in rare cases with severe loss of methionine adenosyltransferase activity.
Mondo Term and Equivalent IDs
MONDO:0009607:  methionine adenosyltransferase deficiency
GARD:0008397: 
NCIT:C123435: 
Orphanet:168598: