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Mitochondrial DNA depletion syndrome, hepatocerebral form

ORPHA:254871

Classification level: Group of disorders
  • Synonym(s):
    • Deoxyguanosine kinase deficiency
    • mtDNA depletion syndrome, hepatocerebral form
  • Prevalence: -
  • Inheritance: Autosomal recessive 
  • Age of onset: Infancy, Neonatal
  • ICD-10: -
  • OMIM: -
  • UMLS: C3711385
  • MeSH: -
  • GARD: -
  • MedDRA: -

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