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Diseases
INTERMEDIARY METABOLISM: NUTRIENTS
1 Disorders of amino acid metabolism
1.5 Disorders of the metabolism of sulfur-containing amino acids
Methionine adenosyltransferase I/III deficiency
Methionine adenosyltransferase II deficiency
Glycine N-methyltransferase deficiency
S-Adenosylhomocysteine hydrolase deficiency
Methionine synthase deficiency
Homocystinuria
Homocystinuria, classical
Cystathioninuria
Genes
Gene products
Pathways
Multimers
More information
About Online IMD
OnlineIMD
Home
Diseases
INTERMEDIARY METABOLISM: NUTRIENTS
1 Disorders of amino acid metabolism
1.5 Disorders of the metabolism of sulfur-containing amino acids
Methionine adenosyltransferase I/III deficiency
Methionine adenosyltransferase II deficiency
Glycine N-methyltransferase deficiency
S-Adenosylhomocysteine hydrolase deficiency
Methionine synthase deficiency
Homocystinuria
Homocystinuria, classical
Cystathioninuria
Genes
Gene products
Pathways
Multimers
More information
About Online IMD
Glycine N-methyltransferase deficiency
(GNMT deficiency)
Type
Disease
External link(s)
Orphanet
IEMbase
VMH
Gene
GNMT
/ Glycine N-methyltransferase
6p21.1
OMIM
GnomAD
Ensembl
HGNC
VMH
LOVD
Gene product
Glycine N-methyltransferase
Pathway
Metabolism of sulfur-containing amino acids and hydrogen sulfide
Disease group(s)
1.5 Disorders of the metabolism of sulfur-containing amino acids