1. Genes and Genomic Entities
  2. DMGDH

DMGDH

dimethylglycine dehydrogenase
OMIM: 605849, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red DMGDH in Undiagnosed metabolic disorders

Level 3: Specific metabolic abnormalities
Level 2: Metabolic disorders
Version 1.617

review Unknown
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Dimethylglycinuria (Disorders and variants of enzymes that oxidise xenobiotics other than cytochrome P450)
  • Dimethylglycine dehydrogenase deficiency 605850
Red DMGDH in Likely inborn error of metabolism - targeted testing not possible


Version 4.137
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood

    		•  review Unknown
    Sources
    • London North GLH
    • NHS GMS
    • Expert Review Red
    Phenotypes
    • Dimethylglycine dehydrogenase deficiency 605850
    • Dimethylglycinuria (Disorders and variants of enzymes that oxidise xenobiotics other than cytochrome P450)