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Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion

MedGen UID:
1826105
Concept ID:
C5680920
Disease or Syndrome
Monarch Initiative: MONDO:0016478
Orphanet: ORPHA231130

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVBeckwith-Wiedemann syndrome due to 11p15 translocation/inversion

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    Genetic Testing Registry

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