Osteogenesis imperfecta
ICD-10 Code
Q78.0
Osteogenesis imperfecta
Definition
Osteogenesis imperfecta (OI) comprises a heterogeneous group of genetic disorders characterized by increased bone fragility, low bone mass, and susceptibility to bone fractures with variable severity.
Also known as brittle bone disease, glass bone disease, Lobstein disease, OI, Osteopsathyrosis, Porak and Durante disease — per MONDO
Also identified as
- DOID 12347 per MONDO
- ICD10CM Q78.0 per MONDO
- ICD9 756.51 per MONDO
- MESH D010013 per MONDO
- NCIT C26837 per MONDO
- Orphanet 666 per MONDO
- SCTID 78314001 per MONDO
- UMLS C0029434 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 |
| 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 |