LD24.K0 Osteogenesis imperfecta
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2026-01
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.
inclusions
- Fragilitas ossium
- Osteopsathyrosis
synonyms
- Osteogenesis imperfecta
- Fragilitas ossium
- OI - [osteogenesis imperfecta]
- Osteopsathyrosis
- blue sclera with fragility of bone and deafness
- bony fragility
- brittle bone disease
- brittle bone syndrome
- ossium fragility
- osteitis fragilitans
- white blue sclera - fragility of bone - deafness
- Osteogenesis imperfecta type 1
- Adair Dighton syndrome
- Eddowes syndrome
- Ekman syndrome
- Ekman-Lobstein syndrome
- Lobstein syndrome
- Spurway syndrome
- Spurway-Eddowes syndrome
- van der Hoeve syndrome
- van der Hoeve-de Kleyn syndrome
- Osteogenesis imperfecta type 2
- Vrolik disease
- Osteogenesis imperfecta type 3
- Osteogenesis imperfecta type 4
- Osteogenesis imperfecta type 5
Thank you for choosing Find-A-Code, please Sign In to remove ads.
Quick, Current, Complete - www.findacode.com