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- B92838621a491945dca2db5bdd13a3c11 hasDbXref "Orphanet:739" @default.
- B92838621a491945dca2db5bdd13a3c11 type Axiom @default.
- B92838621a491945dca2db5bdd13a3c11 annotatedProperty IAO_0000115 @default.
- B92838621a491945dca2db5bdd13a3c11 annotatedSource MONDO_0008300 @default.
- B92838621a491945dca2db5bdd13a3c11 annotatedTarget "Prader-Willi syndrome is a rare genetic disorder characterized by hypothalamic-pituitary abnormalities with severe hypotonia during the neonatal period and first two years of life and the onset of hyperphagia with a risk of morbid obesity during infancy and adulthood, learning difficulties and behavioral problems or severe psychiatric problems." @default.