Ollier disease
ICD-10 Code
Q78.4
Ollier 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.
Also known as dyschondroplasia, Ollier disease, Ollier type enchondromatosis, Ollier's disease, osteochondromatosis — per MONDO
Also identified as
- DOID 4624 per MONDO
- ICD10CM Q78.4 per MONDO
- NCIT C3008 per MONDO
- OMIM 166000 per MONDO
- Orphanet 296 per MONDO
- SCTID 268274005 per MONDO
- UMLS C0014084 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Bone element | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Bone element | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Cartilage | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Connective tissue | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Musculoskeletal system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Musculoskeletal system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |