LD24.K0 Osteogenesis imperfecta
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
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
- Osteopsathyrosis
- brittle bone disease
- brittle bone syndrome
- OI - [osteogenesis imperfecta]
- ossium fragility
- osteitis fragilitans
- bony fragility
- blue sclera with fragility of bone and deafness
- white blue sclera - fragility of bone - deafness
- Osteogenesis imperfecta type 1
- van der Hoeve syndrome
- Ekman-Lobstein syndrome
- van der Hoeve-de Kleyn syndrome
- Ekman syndrome
- Lobstein syndrome
- Eddowes syndrome
- Spurway-Eddowes syndrome
- Spurway syndrome
- Adair Dighton syndrome
- Osteogenesis imperfecta type 2
- Vrolik disease
- Osteogenesis imperfecta type 3
- Osteogenesis imperfecta type 4
- Osteogenesis imperfecta type 5
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