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- B4de623a3747f4e8ac506b156df229ee8 hasDbXref "Orphanet:178509" @default.
- B4de623a3747f4e8ac506b156df229ee8 type Axiom @default.
- B4de623a3747f4e8ac506b156df229ee8 annotatedProperty IAO_0000115 @default.
- B4de623a3747f4e8ac506b156df229ee8 annotatedSource MONDO_0008201 @default.
- B4de623a3747f4e8ac506b156df229ee8 annotatedTarget "Perry syndrome is a rare inherited neurodegenerative disorder characterized by rapidly progressive early-onset parkinsonism, central hypoventilation, weight loss, insomnia and depression." @default.