Disease: Hypermethioninemia due to deficiency of glycine N-methyltransferase ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hypermethioninemia due to deficiency of glycine N-methyltransferase
CUI: C1847720
Disease: Hypermethioninemia due to deficiency of glycine N-methyltransferase
0.800 GeneticVariation UNIPROT Glycine N -methyltransferase deficiency: a new patient with a novel mutation. 14739680 2003
Hypermethioninemia due to deficiency of glycine N-methyltransferase
CUI: C1847720
Disease: Hypermethioninemia due to deficiency of glycine N-methyltransferase
0.800 GeneticVariation UNIPROT Mutations in human glycine N-methyltransferase give insights into its role in methionine metabolism. 11810299 2002
Hypermethioninemia due to deficiency of glycine N-methyltransferase
CUI: C1847720
Disease: Hypermethioninemia due to deficiency of glycine N-methyltransferase
0.800 CausalMutation CLINVAR