Hypermethioninemia (MET)

Alias:
Hepatic Methionine Adenosyltransferase Deficiency
Glycine N-Methyltransferase Deficiency
Met
Deficiency of Methionine Adenosyltransferase
S-Adenosylhomocysteine Hydrolase Deficiency
Deficiency of Acetyl-Coa Acetyltransferase
Methionine Adenosyltransferase Deficiency
Gnmt Deficiency
Mat Deficiency
Methioninemia
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hypermethioninemia, also known as hepatic methionine adenosyltransferase deficiency, is related to methionine adenosyltransferase i/iii deficiency and glycine n-methyltransferase deficiency, and has symptoms including vomiting An important gene associated with Hypermethioninemia is MAT1A (Methionine Adenosyltransferase 1A), and among its related pathways/superpathways are Metabolism and Regulation of expression of SLITs and ROBOs. The drugs Lecithin and Racemethionine have been mentioned in the context of this disorder. Affiliated tissues include liver and eye, and related phenotypes are Decreased shRNA abundance and liver/biliary system
Related ID:
MESH:C564683

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Antenatal
--
17
103
28

Medical Symptom

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Gene & Mutation

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Disease Model

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References Literature

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