LA07.3ICD-11 MMS 2026-01
Primary syringomyelia or hydromyelia
Description
A condition caused by failure of the spinal canal to correctly develop during the antenatal period. This condition is characterised by a cavity within the spinal cord in which cerebrospinal fluid can accumulate. Confirmation is through observation of a fluid filled cavity within the spinal cord by imaging.
Index terms
- Primary syringomyelia or hydromyelia
- Congenital syringomyelia or hydromyelia
- Congenital hydromyelia
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- Hydromyelia
- Hydrorachis
- Primary syringomyelia
Excludes
Exclusions from above levels
- http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism
Sibling codes
LA07.0– Primary tethered cord syndromeLA07.1– DiastematomyeliaLA07.2– AmyeliaLA07.4– 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 entity
Primary syringomyelia or hydromyelia – http://id.who.int/icd/entity/465198086
Part of: LA07: Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column › 20: Developmental anomalies