OnlineIMD

Mitochondrial DNA depletion syndromes

(MDDS)
  • Type
    Phenotype
  • External link(s)
    • Orphanet
  • Parent entry
    • 12.1    Syndromic mitochondrial disorders
  • Child entries
    • MDDS, hepatocerebral form
    • Navajo neurohepatopathy
    • MDDS, cerebrorenal form
    • MDDS, hepatocerebrorenal form
    • MDDS with progressive myopathy
    • MDDS with myopathy and cardiomyopathy
    • MDDS with encephalomyopathy