Hepatic methionine adenosyltransferase deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
HEPATIC METHIONINE ADENOSYLTRANSFERASE DEFICIENCY
C0268621
MAT1A Causal — ClinVar, Disgenet
AHCY Unknown — Disgenet
GNMT Unknown — Disgenet
All3 Causal1 Unknown2
Related Diseases Diseases that share the most curated genes with Hepatic methionine adenosyltransferase deficiency.
5 View disease cluster →
S-adenosylhomocysteine hydrolase deficiency 3 shared genesAHCY, MAT1A, GNMT Related via 3 shared genes including AHCY, MAT1A, GNMT. Sulfur amino acid metabolism disorder 2 shared genesAHCY, GNMT Related via 2 shared genes including AHCY, GNMT. hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase 1 shared geneAHCY Related via 1 shared gene including AHCY. methionine adenosyltransferase deficiency 1 shared geneMAT1A Related via 1 shared gene including MAT1A. Glycine n-methyltransferase deficiency 1 shared geneGNMT Related via 1 shared gene including GNMT.