ORPHA:1458
CODAS syndrome
Also called Cerebrooculodentoauriculoskeletal syndrome
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:1458 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Epicanthus
- Overfolded helix
- Anteverted nares
- Cataract
- Abnormality of dental enamel
- Delayed eruption of teeth