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- B4179196b44d4f8a06c27302a92ce1685 hasDbXref "Orphanet:193" @default.
- B4179196b44d4f8a06c27302a92ce1685 type Axiom @default.
- B4179196b44d4f8a06c27302a92ce1685 annotatedProperty IAO_0000115 @default.
- B4179196b44d4f8a06c27302a92ce1685 annotatedSource MONDO_0008999 @default.
- B4179196b44d4f8a06c27302a92ce1685 annotatedTarget "Cohen syndrome (CS) is a rare genetic developmental disorder characterized by microcephaly, characteristic facial features, hypotonia, non-progressive intellectual deficit, myopia and retinal dystrophy, neutropenia and truncal obesity." @default.