OnlineIMD

CLPP deficiency

  • Synonym(s)
    • Perrault syndrome type 3
  • Type
    Disease
  • External link(s)
    • IEMbase
  • Gene
    • CLPP / CLPP mitochondrial peptidase
      • 19p13.3
      • OMIM
      • GnomAD
      • Ensembl
      • HGNC
      • VMH
      • LOVD
  • Gene product
    • Mitochondrial matrix peptidase
  • Disease group(s)
    • 11.3    Disorders of mitochondrial protein quality control