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- B5fe553dc8849e0be1570e315d47f0684 hasDbXref "Orphanet:2332" @default.
- B5fe553dc8849e0be1570e315d47f0684 type Axiom @default.
- B5fe553dc8849e0be1570e315d47f0684 annotatedProperty IAO_0000115 @default.
- B5fe553dc8849e0be1570e315d47f0684 annotatedSource MONDO_0007846 @default.
- B5fe553dc8849e0be1570e315d47f0684 annotatedTarget "KBG syndrome is a rare condition characterized by a typical facial dysmorphism, macrodontia of the upper central incisors, skeletal (mainly costovertebral) anomalies and developmental delay." @default.