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- B1ce984f98091f24d88a8de1bde174e4f hasDbXref "Orphanet:726" @default.
- B1ce984f98091f24d88a8de1bde174e4f type Axiom @default.
- B1ce984f98091f24d88a8de1bde174e4f annotatedProperty IAO_0000115 @default.
- B1ce984f98091f24d88a8de1bde174e4f annotatedSource MONDO_0008758 @default.
- B1ce984f98091f24d88a8de1bde174e4f annotatedTarget "Alpers Huttenlocher syndrome (AHS) is a cerebrohepatopathy and a rare and severe form of mitochondrial DNA (mtDNA) depletion syndrome characterized by the triad of progressive developmental regression, intractable seizures, and hepatic failure." @default.