Glycine n-methyltransferase deficiency

Log in to bookmark this disease

Bookmark This Disease

Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
GLYCINE N-METHYLTRANSFERASE DEFICIENCY
606664MONDO:0011698
GNMT Causal
11810299 14739680 17937387 26990548 27207470
ClinGen, ClinVar, GWAS catalog, HPO
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Glycine n-methyltransferase deficiency.
5 View disease cluster →
S-adenosylhomocysteine hydrolase deficiency 1 shared geneGNMT Related via 1 shared gene including GNMT. Sulfur amino acid metabolism disorder 1 shared geneGNMT Related via 1 shared gene including GNMT. Hepatic methionine adenosyltransferase deficiency 1 shared geneGNMT Related via 1 shared gene including GNMT. Hyperhomocysteinemia 1 shared geneGNMT Related via 1 shared gene including GNMT. Peroxisome biogenesis disorder 1 shared geneGNMT Related via 1 shared gene including GNMT.