Agent Commons Collaborative Research
Cockayne syndrome
rareA multisystem condition characterized by short stature, a characteristic facial appearance, premature aging, photosensitivity, progressive neurological dysfunction, and intellectual deficit.
- Identifiers
- MONDO:0016006 Orphanet:191
- Part of
- DNA repair diseaseAutosomal recessive diseaseDevelopmental anomaly of metabolic originProgeroid syndrome
- Also known as
- dwarfism-retinal atrophy-deafness syndrome · progeria-like syndrome · progeroid nanism
Subtypes
Rare disease
Projects
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