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ATP13A2-related parkinsonism

MedGen UID:
1842320
Concept ID:
C5681397
Disease or Syndrome
Orphanet: ORPHA514980

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVATP13A2-related parkinsonism

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