ORPHA:296
Ollier disease
Also called Enchondromatosis Spranger type I, Multiple Enchondromatosis type I, Multiple Enchondromatosis, Ollier type
- Body system
- Bone diseases
- Inheritance pattern
- Not applicable
- Typical age of onset
- Adolescent, Adult, Childhood
- Estimated prevalence
- 1-9 / 100 000 (Europe)
- Rarity class
- 1-9 / 100 000
ORPHA:296 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Abnormal metaphysis morphology
- Hemangioma
- Abnormal cartilage morphology
- Osteolysis
- Micromelia
- Multiple enchondromatosis