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- B429c76f2df30ee88f323bb0db8c3b20c NCIT_P378 "NCI" @default.
- B429c76f2df30ee88f323bb0db8c3b20c type Axiom @default.
- B429c76f2df30ee88f323bb0db8c3b20c annotatedProperty IAO_0000115 @default.
- B429c76f2df30ee88f323bb0db8c3b20c annotatedSource NCIT_C185241 @default.
- B429c76f2df30ee88f323bb0db8c3b20c annotatedTarget "A chromosomal anomaly characterized by the partial duplication of the short arm of chromosome 2. The phenotype is highly variable but principally characterized by growth failure, global developmental delay, facial dysmorphism and ocular anomalies." @default.