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Bryant-Li-Bhoj neurodevelopmental syndrome

MedGen UID:
Concept ID:
Disease or Syndrome
Related genes: H3-3B, H3-3A
Monarch Initiative: MONDO:0031200
OMIM® Phenotypic series: PS619720

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  

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