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- B48ec6ccd14de56f3709e21c436f5fab4 hasDbXref "Orphanet:171829" @default.
- B48ec6ccd14de56f3709e21c436f5fab4 type Axiom @default.
- B48ec6ccd14de56f3709e21c436f5fab4 annotatedProperty IAO_0000115 @default.
- B48ec6ccd14de56f3709e21c436f5fab4 annotatedSource MONDO_0015749 @default.
- B48ec6ccd14de56f3709e21c436f5fab4 annotatedTarget "Deletion 6q16 syndrome is a Prader-Willi like syndrome characterized by obesity, hyperphagia, hypotonia, small hands and feet, eye/vision anomalies, and global developmental delay." @default.