OnlineIMD

11.1    Disorders of mitochondrial shuttles and carriers

  • Type
    Group
  • Disease group(s)
    • 11    Other disorders of mitochondrial function
  • Child entries
    • Mitochondrial pyruvate carrier deficiency
    • Mitochondrial citrate carrier deficiency
    • Mitochondrial phosphate carrier deficiency
    • Mitochondrial thiamine pyrophosphate transporter deficiency
    • Adenine nucleotide translocator deficiency
    • Mitochondrial dicarboxylate transporter deficiency
    • Carnitine-acylcarnitine translocase deficiency
    • Mitochondrial flavin adenine dinucleotide transporter deficiency
    • Mitochondrial coenzyme A transporter deficiency
    • Mitochondrial oxoglutarate/malate carrier deficiency
    • Cytosolic glycerol-3-phosphate dehydrogenase deficiency
    • Mitochondrial ornithine transporter deficiency
    • Mitochondrial oxodicarboxylate carrier deficiency
    • Aralar deficiency
    • Mitochondrial glutamate transporter deficiency
    • Mitochondrial ATP-Mg/phosphate transporter deficiency
    • Citrin deficiency
    • Cytosolic malate dehydrogenase deficiency
    • S-adenosylmethionine carrier deficiency
    • Mitochondrial aspartate aminotransferase deficiency
    • Mitochondrial pyrimidine nucleotide carrier deficiency
    • Mitochondrial glycine transporter deficiency
    • UGO-1 like protein deficiency
    • Mitochondrial calcium uniporter deficiency
    • Mitochondrial calcium uniporter 2 deficiency