LB73.25ICD-11 MMS 2026-01
Congenital scoliosis due to congenital bony malformation
Description
A condition caused by malformation of the ribs or spine. This condition is characterised by abnormal curving of the spine.
Index terms
- Congenital scoliosis due to congenital bony malformation
- congenital scoliosis due to anomalies of vertebra
- Congenital scoliosis with failure of hemivertebra segmentation
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- congenital scoliosis with failure of segmentation
- failure of hemivertebra segmentation with scoliosis
- Hemivertebra fusion or failure of segmentation with scoliosis
- Congenital scoliosis with hemivertebra fusion
- hemivertebra fusion with scoliosis
- Single hemivertebra with congenital scoliosis
- Congenital scoliosis due to absence of vertebra
Excludes
LB73.2Y– congenital scoliosis NOS
Exclusions from above levels
- http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism
Sibling codes
LB73.20– Klippel-Feil anomalyLB73.21– Occipitalisation of atlasLB73.22– Atlanto-axial instability or subluxationLB73.23– Aplasia or hypoplasia of the odontoid process of axisLB73.24– Segmentation anomalies of vertebraeLB73.26– Sacralisation of the last lumbar vertebraLB73.27– Lumbarisation of the first sacral vertebraLB73.28– Sacrum agenesis or hypoplasiaLB73.29– Caudal appendageLB73.2A– Congenital spondylolisthesisLB73.2Y– Other specified structural developmental anomalies of spineLB73.2Z– Structural developmental anomalies of spine, unspecified
Foundation entity
Congenital scoliosis due to congenital bony malformation – http://id.who.int/icd/entity/1852308037
Allowed postcoordination axes
Part of: LB73.2: Structural developmental anomalies of spine › LB73: Structural developmental anomalies of spine or bony thorax › 20: Developmental anomalies