hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase
AHCY Causal
31957987 20852937 30121674
ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase.
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S-adenosylhomocysteine hydrolase deficiency 1 shared geneAHCY Related via 1 shared gene including AHCY. Sulfur amino acid metabolism disorder 1 shared geneAHCY Related via 1 shared gene including AHCY. Hepatic methionine adenosyltransferase deficiency 1 shared geneAHCY Related via 1 shared gene including AHCY. Amino acid metabolism disorder 1 shared geneAHCY Related via 1 shared gene including AHCY. Hepatolenticular degeneration 1 shared geneAHCY Related via 1 shared gene including AHCY.