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- B87346318e978cefb8a56f1c72171afb0 hasDbXref "NCIT:C131647" @default.
- B87346318e978cefb8a56f1c72171afb0 type Axiom @default.
- B87346318e978cefb8a56f1c72171afb0 annotatedProperty IAO_0000115 @default.
- B87346318e978cefb8a56f1c72171afb0 annotatedSource MONDO_0009865 @default.
- B87346318e978cefb8a56f1c72171afb0 annotatedTarget "A rare, autosomal recessive, inherited disorder caused by mutation of the PGAM2 gene. It is characterized by non-spherocytic hemolytic anemia, exercise-induced cramping, myoglobinuria, and presence of tubular aggregates on muscle biopsy." @default.