Orphanet: Ollier disease

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Ollier disease

Disease definition

A rare primary bone dysplasia disorder characterized by the development of multiple mainly unilateral or asymmetrically distributed enchondromas throughout the metaphyses of the long bones.

ORPHA:296

Classification level: Disorder

Synonym(s):
- Dyschondroplasia
Prevalence: 1-9 / 100 000
Inheritance: Not applicable
Age of onset: Adolescent, Adult, Childhood
ICD-10: Q78.4
OMIM: 166000
UMLS: C0013366 C0014084
MeSH: D004687
GARD: 7251
MedDRA: 10014642

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Ollier disease

ORPHA:296

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