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- B017d521bc50b1b27d099b5b3119fdd4e NCIT_P378 "NCI" @default.
- B017d521bc50b1b27d099b5b3119fdd4e type Axiom @default.
- B017d521bc50b1b27d099b5b3119fdd4e annotatedProperty IAO_0000115 @default.
- B017d521bc50b1b27d099b5b3119fdd4e annotatedSource NCIT_C131837 @default.
- B017d521bc50b1b27d099b5b3119fdd4e annotatedTarget "Hyperinsulinism due to inactivating mutation(s) in the gene HADH, encoding mitochondrial (short-chain) hydroxyacyl-coenzyme A dehydrogenase, resulting in loss of inhibition of glutamate dehydrogenase (GDH). This condition is also characterized by protein-induced hypoglycemia, but in contrast to GLUD1-associated hyperinsulinism, hyperammonemia is absent." @default.