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- Bd5aa39298948ed1d4efda4f26d3d751a hasDbXref "Orphanet:364063" @default.
- Bd5aa39298948ed1d4efda4f26d3d751a type Axiom @default.
- Bd5aa39298948ed1d4efda4f26d3d751a annotatedProperty IAO_0000115 @default.
- Bd5aa39298948ed1d4efda4f26d3d751a annotatedSource MONDO_0018226 @default.
- Bd5aa39298948ed1d4efda4f26d3d751a annotatedTarget "Infantile epileptic-dyskinetic encephalopathy is a monogenic disease with epilepsy characterized by developmental delay and infantile spasms in the first months of life, followed by chorea and generalized dystonia and progressing to quadriplegic dyskinesia, recurrent status dystonicus, intractable focal epilepsy and severe intellectual disability." @default.