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Congenital intestinal disease due to an enzymatic defect

MedGen UID:
1843338
Concept ID:
C5681744
Disease or Syndrome
Orphanet: ORPHA104006

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVCongenital intestinal disease due to an enzymatic defect

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