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- NCIT_C122923 IAO_0000115 "A genetic condition caused by mutation(s) in the ABCC8 gene, encoding ATP-binding cassette sub-family C member 8." @default.
- NCIT_C122923 NCIT_NHC0 "C122923" @default.
- NCIT_C122923 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C122923 NCIT_P108 "Persistent Hyperinsulinemic Hypoglycemia of Infancy" @default.
- NCIT_C122923 NCIT_P207 "C3888018" @default.
- NCIT_C122923 NCIT_P322 "Cellosaurus" @default.
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- NCIT_C122923 NCIT_R104 NCIT_C13055 @default.
- NCIT_C122923 NCIT_R104 NCIT_C21599 @default.
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- NCIT_C122923 NCIT_R176 NCIT_C21295 @default.
- NCIT_C122923 NCIT_R176 NCIT_C28533 @default.
- NCIT_C122923 normalizedInformationContent "100" @default.
- NCIT_C122923 referenceCount "1" @default.
- NCIT_C122923 hasExactSynonym "Familial Hyperinsulinemic Hypoglycemia-1" @default.
- NCIT_C122923 hasExactSynonym "HHF1" @default.
- NCIT_C122923 hasExactSynonym "PHHI" @default.
- NCIT_C122923 hasExactSynonym "Persistent Hyperinsulinemic Hypoglycemia of Infancy" @default.
- NCIT_C122923 inSubset NCIT_C165258 @default.
- NCIT_C122923 inSubset NCIT_C192842 @default.
- NCIT_C122923 type Class @default.
- NCIT_C122923 isDefinedBy ncit.owl @default.
- NCIT_C122923 label "Persistent Hyperinsulinemic Hypoglycemia of Infancy" @default.
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- NCIT_C122923 subClassOf NCIT_C7057 @default.