| Corneodermatoosseous syndrom | |
| Synonyms: | CDO syndrome[1] |
| Field: | Medical genetics |
Corneodermatosseous syndrome is an autosomal dominant condition with onset in infancy, characterized by corneal dystrophy, photophobia, diffuse palmoplantar keratoderma, distal onycholysis, skeletal abnormalities, with brachydactyly, short stature, and medullary narrowing of digits.