MeSH Browser

MeSH Supplementary: Hypermethioninemia
Unique ID: C564683
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564683
Entry Term(s): Deficiency of Methionine Adenosyltransferase; GNMT Deficiency; Glycine N-Methyltransferase Deficiency; Hepatic Methionine Adenosyltransferase Deficiency; Hypermethioninemia with Deficiency of S-Adenosylhomocysteine Hydrolase; Hypermethioninemia, Isolated Persistent; Methionine Adenosyltransferase Deficiency; Methioninemia; S-Adenosylhomocysteine Hydrolase Deficiency
Registry Numbers: 0
Heading Mapped to: *Amino Acid Metabolism, Inborn Errors; Glycine N-Methyltransferase / deficiency
Frequency: 46
Note: mutation in GNMT, MAT1A, AHCY
Date of Entry: 2012/11/05
Revision Date: 2015/08/18

Hypermethioninemia MeSH Supplementary Concept Data 2025