PanelApp (staging)
  1. Genes and Genomic Entities
  2. DMGDH

DMGDH

dimethylglycine dehydrogenase
OMIM: 605849, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber DMGDH in Mendeliome


Version 1.2302

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Dimethylglycine dehydrogenase deficiency MIM#605850
  • Disorders and variants of other enzymes that oxidise xenobiotics

Amber DMGDH in Miscellaneous Metabolic Disorders


Level 2: Metabolic disorders
Version 1.48

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Dimethylglycine dehydrogenase deficiency MIM#605850
    • Disorders and variants of other enzymes that oxidise xenobiotics

    Red DMGDH in Aminoacidopathy


    Level 2: Metabolic disorders
    Version 1.133

    Component of the following Super Panels:

  • Metabolic Disorders Superpanel

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • ClinGen
    Phenotypes
    • dimethylglycine dehydrogenase deficiency MONDO:0011610