Osteogenesis imperfecta (Q46605)
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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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD24.K0 |
||
| English | 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. |
Statements
CID11:LD24.K0
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dki-india-LD24.K0
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Concluído
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13 August 2026
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