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EGF-related primary hypomagnesemia with intellectual disability

MedGen UID:
1843381
Concept ID:
C5681825
Disease or Syndrome
Monarch Initiative: MONDO:0850088
Orphanet: ORPHA620368

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVEGF-related primary hypomagnesemia with intellectual disability

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