OnlineIMD

Mitochondrial phosphate carrier deficiency

  • Type
    Disease
  • External link(s)
    • Orphanet
    • IEMbase
  • Gene
    • SLC25A3 / Solute Carrier Family 25 Member 3
      • 12q23.1
      • OMIM
      • GnomAD
      • Ensembl
      • HGNC
      • VMH
      • LOVD
  • Gene product
    • Phosphate carrier protein, mitochondrial
  • Disease group(s)
    • 11.1    Disorders of mitochondrial shuttles and carriers