DMGDH

dimethylglycine dehydrogenase
OMIM: 605849, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red DMGDH in Mendeliome


Version 1.3512

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Red
Phenotypes
  • Dimethylglycine dehydrogenase deficiency MIM#605850

Red DMGDH in Miscellaneous Metabolic Disorders


Level 2: Metabolic disorders
Version 1.57

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • 2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Dimethylglycine dehydrogenase deficiency MIM#605850

    Red DMGDH in Aminoacidopathy


    Level 2: Metabolic disorders
    Version 1.137

    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