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Parkinsonism due to ATP13A2 deficiency

ORPHA:314632

  • Synonym(s):
    • CLN12 disease
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal recessive 
  • Age of onset: Childhood
  • ICD-10: E75.4
  • OMIM: 606693
  • UMLS: -
  • MeSH: -
  • GARD: -
  • MedDRA: -

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