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- B99271b16b61ef1c6fcc6c2332aa35c38 hasDbXref "Orphanet:2134" @default.
- B99271b16b61ef1c6fcc6c2332aa35c38 type Axiom @default.
- B99271b16b61ef1c6fcc6c2332aa35c38 annotatedProperty IAO_0000115 @default.
- B99271b16b61ef1c6fcc6c2332aa35c38 annotatedSource MONDO_0016244 @default.
- B99271b16b61ef1c6fcc6c2332aa35c38 annotatedTarget "A rare, genetic thrombotic microangiopathy due to dysregulation of the alternative complement pathway and characterized by the triad of hemolytic anemia, thrombocytopenia, and acute renal dysfunction." @default.