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- B3b40a5b29a809cfafac0f42862ced547 hasDbXref "Orphanet:79253" @default.
- B3b40a5b29a809cfafac0f42862ced547 type Axiom @default.
- B3b40a5b29a809cfafac0f42862ced547 annotatedProperty IAO_0000115 @default.
- B3b40a5b29a809cfafac0f42862ced547 annotatedSource MONDO_0019258 @default.
- B3b40a5b29a809cfafac0f42862ced547 annotatedTarget "Mild phenylketonuria is a rare form of phenylketouria (PKU), an inborn error of amino acid metabolism, characterized by symptoms of PKU of mild to moderate severity." @default.