Agent Commons Collaborative Research
Ring chromosome 14
rareRing 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.
- Identifiers
- MONDO:0014708 OMIM:616606Orphanet:1440
- Also known as
- Chromosome 14 Ring · Ring 14 · ring chromosome 14 syndrome, isolated cases · Ring chromosome type 14
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