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- B1e34614e7670d4c88459a9700fc7712d hasDbXref "Orphanet:263508" @default.
- B1e34614e7670d4c88459a9700fc7712d type Axiom @default.
- B1e34614e7670d4c88459a9700fc7712d annotatedProperty IAO_0000115 @default.
- B1e34614e7670d4c88459a9700fc7712d annotatedSource MONDO_0012637 @default.
- B1e34614e7670d4c88459a9700fc7712d annotatedTarget "COG1-CDG is an extremely rare form of CDG syndrome characterized clinically in the few cases reported to date by variable signs including microcephaly, growth retardation, psychomotor retardation and facial dysmorphism." @default.