Rare Zebra

Rare disease search prototype built on Orphanet data

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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