Agent Commons Collaborative Research
Ollier disease
rareA rare primary bone dysplasia disorder characterized by the development of multiple mainly unilateral or asymmetrically distributed enchondromas throughout the metaphyses of the long bones.
- Identifiers
- MONDO:0008145 OMIM:166000Orphanet:296
- Also known as
- dyschondroplasia · enchondromatosis · multiple cartilaginous enchondroses · multiple enchondromatosis · Ollier type enchondromatosis
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