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- Bcf316fb58d3afd56a739dbbc5f4c54ef NCIT_P378 "NCI" @default.
- Bcf316fb58d3afd56a739dbbc5f4c54ef type Axiom @default.
- Bcf316fb58d3afd56a739dbbc5f4c54ef annotatedProperty IAO_0000115 @default.
- Bcf316fb58d3afd56a739dbbc5f4c54ef annotatedSource NCIT_C114769 @default.
- Bcf316fb58d3afd56a739dbbc5f4c54ef annotatedTarget "A rare autosomal dominant form of diabetes mellitus affecting young people with a positive family history. MODY is a form of monogenic diabetes, resulting from mutations in a single gene. The most common forms are HNF1alpha-MODY (MODY3) and GCK-MODY (MODY2), due to mutations in the HNF1A and GCK genes, respectively." @default.