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- Bf822e5e561a00248448cecce3cc86572 hasDbXref "NCIT:C129741" @default.
- Bf822e5e561a00248448cecce3cc86572 type Axiom @default.
- Bf822e5e561a00248448cecce3cc86572 annotatedProperty IAO_0000115 @default.
- Bf822e5e561a00248448cecce3cc86572 annotatedSource MONDO_0007453 @default.
- Bf822e5e561a00248448cecce3cc86572 annotatedTarget "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.