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- B05d7c36da9a95d63a7d816210ec5f5f7 hasDbXref "Orphanet:1440" @default.
- B05d7c36da9a95d63a7d816210ec5f5f7 type Axiom @default.
- B05d7c36da9a95d63a7d816210ec5f5f7 annotatedProperty IAO_0000115 @default.
- B05d7c36da9a95d63a7d816210ec5f5f7 annotatedSource MONDO_0014708 @default.
- B05d7c36da9a95d63a7d816210ec5f5f7 annotatedTarget "Ring chromosome 14 syndrome is characterized by intellectual deficit, retinal and skin pigmentation disorders, seizures, and dysmorphic features, including flat occiput, epicanthal folds, downward slanting eyes, flat nasal bridge, upturned nostrils, short neck, and large low set ears." @default.