ICD-11 classes
20 Developmental anomalies
Multiple developmental anomalies or syndromes
LD24 — Syndromes with skeletal anomalies as a major feature
LD24.2 — Bone diseases with disorganised development of skeletal...
LD24.K0 — Osteogenesis imperfecta
ICD-11 LD24.K0 — Osteogenesis imperfecta
Osteogenesis imperfecta (OI) comprises a heterogeneous group of genetic disorders characterised by increased bone fragility, low bone mass, and susceptibility to bone fractures with variable severity. The most clinically relevant characteristic of all types of OI is bone fragility, which manifests as multiple spontaneous fractures.
It includes 2 items.
- Fragilitas ossium
- Osteopsathyrosis
The diagnosis excludes nothing.
It has no clarifying diagnoses.
The diagnosis is coded elsewhere:
- Certain specified disorders of bone density or structure #17974
- Genetic bone diseases with decreased bone density #18039
- Bone diseases with disorganised development of skeletal components #18074
- Bone diseases with disorganised development of skeletal components #18749
- Genetic bone diseases with decreased bone density #18798
- Genetic bone diseases with decreased bone density #23289