LB73.21ICD-11 MMS 2026-01
Occipitalisation of atlas
Description
A condition caused by failure of the atlas and occiput to correctly develop during the antenatal period. This condition is characterised by fusion of the atlas to the base of the occiput. This condition may present with headache, suboccipital stiffness, restricted motion, or dizziness. Confirmation is through observation of the fusion by imaging.
Index terms
- Occipitalisation of atlas
Exclusions from above levels
- http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism
Sibling codes
LB73.20– Klippel-Feil anomalyLB73.22– 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
Foundation entity
Occipitalisation of atlas – http://id.who.int/icd/entity/1814363019
Allowed postcoordination axes
Part of: LB73.2: Structural developmental anomalies of spine › LB73: Structural developmental anomalies of spine or bony thorax › 20: Developmental anomalies