LB73.2ICD-11 MMS 2026-01
Structural developmental anomalies of spine
Description
Any condition caused by failure of the spine to correctly develop during the antenatal period.
Exclusions from above levels
- http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism
Child 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 vertebraeLB73.25– Congenital scoliosis due to congenital bony malformationLB73.26– 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
Sibling codes
Foundation entity
Structural developmental anomalies of spine – http://id.who.int/icd/entity/2025976730
Allowed postcoordination axes
Part of: LB73: Structural developmental anomalies of spine or bony thorax › 20: Developmental anomalies