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- Be210697f1134f3f5b67b3cdd8abd5c89 hasDbXref "Orphanet:718" @default.
- Be210697f1134f3f5b67b3cdd8abd5c89 type Axiom @default.
- Be210697f1134f3f5b67b3cdd8abd5c89 annotatedProperty IAO_0000115 @default.
- Be210697f1134f3f5b67b3cdd8abd5c89 annotatedSource MONDO_0009869 @default.
- Be210697f1134f3f5b67b3cdd8abd5c89 annotatedTarget "Pierre-Robin syndrome (or Pierre-Robin sequence) is characterized by triad of orofacial morphological anomalies consisting of retrognathism, glossoptosis and a posterior median velopalatal cleft." @default.