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- NCIT_C129741 IAO_0000115 "Monogenic diabetes caused by inactivating mutation(s) in the GCK gene, encoding glucokinase. Heterozygous GCK mutations may manifest as mild hyperglycemia, which is not progressive, and usually requires no treatment. Homozygous GCK mutations result in permanent neonatal diabetes." @default.
- NCIT_C129741 NCIT_NHC0 "C129741" @default.
- NCIT_C129741 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C129741 NCIT_P108 "Glucokinase-Associated Diabetes Mellitus" @default.
- NCIT_C129741 NCIT_P207 "C0342277" @default.
- NCIT_C129741 NCIT_P322 "Cellosaurus" @default.
- NCIT_C129741 NCIT_P322 "NICHD" @default.
- NCIT_C129741 NCIT_P325 "Monogenic diabetes caused by inactivating mutation(s) in the GCK gene, encoding glucokinase. Heterozygous GCK mutations may manifest as mild hyperglycemia, which is not progressive, and usually requires no treatment. Homozygous GCK mutations result in permanent neonatal diabetes." @default.
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- NCIT_C129741 referenceCount "1" @default.
- NCIT_C129741 hasExactSynonym "GCK-Associated Diabetes Mellitus" @default.
- NCIT_C129741 hasExactSynonym "Glucokinase-Associated Diabetes Mellitus" @default.
- NCIT_C129741 hasExactSynonym "MODY2" @default.
- NCIT_C129741 hasExactSynonym "Maturity-Onset Diabetes of the Young, Type 2" @default.
- NCIT_C129741 inSubset NCIT_C118467 @default.
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- NCIT_C129741 type Class @default.
- NCIT_C129741 isDefinedBy ncit.owl @default.
- NCIT_C129741 label "Glucokinase-Associated Diabetes Mellitus" @default.
- NCIT_C129741 subClassOf NCIT_C114769 @default.
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