DMGDH

dimethylglycine dehydrogenase
OMIM: 605849, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red DMGDH in Mendeliome


Version 2.0

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 2.0

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 2.0

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