LA07ICD-11 MMS 2026-01
Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column
Description
Any condition caused by failure of the neurenteric canal, spinal cord and vertebral column to correctly develop during the antenatal period.
Exclusions from above levels
- http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism
Child codes
LA07.0– Primary tethered cord syndromeLA07.1– DiastematomyeliaLA07.2– AmyeliaLA07.3– Primary syringomyelia or hydromyeliaLA07.4– Arnold-Chiari malformation type ILA07.Y– Other specified structural developmental anomalies of the neurenteric canal, spinal cord or vertebral columnLA07.Z– Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column, unspecified
Foundation children elsewhere
LB73.0– Occult spinal dysraphism
Sibling codes
LA00– Anencephaly or similar anomaliesLA01– CephaloceleLA02– Spina bifidaLA03– Arnold-Chiari malformation type IILA04– Congenital hydrocephalusLA05– Cerebral structural developmental anomaliesLA06– Cerebellar structural developmental anomaliesLA0Y– Other specified structural developmental anomalies of the nervous systemLA0Z– Structural developmental anomalies of the nervous system, unspecified
Foundation entity
Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column – http://id.who.int/icd/entity/725439990
Allowed postcoordination axes
Part of: 20: Developmental anomalies