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- Bf9df91254f81dacc4ee95a0c0693e8f5 hasDbXref "Orphanet:2802" @default.
- Bf9df91254f81dacc4ee95a0c0693e8f5 type Axiom @default.
- Bf9df91254f81dacc4ee95a0c0693e8f5 annotatedProperty IAO_0000115 @default.
- Bf9df91254f81dacc4ee95a0c0693e8f5 annotatedSource MONDO_0010524 @default.
- Bf9df91254f81dacc4ee95a0c0693e8f5 annotatedTarget "A rare syndromic, inherited form of sideroblastic anemia in which the cause of the disease is a mutation in the ABCB7 gene and is characterized by mild to moderate anemia (with hypochromia and microcytosis) and early-onset, non- or slowly progressive spinocerebellar ataxia." @default.