LA05ICD-11 MMS 2026-01
Cerebral structural developmental anomalies
Description
Any condition caused by failure of the brain to correctly develop during the antenatal period.
Excludes
LA01– Encephalocele
Exclusions from above levels
- http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism
Child codes
LA05.0– MicrocephalyLA05.1– MegalencephalyLA05.2– HoloprosencephalyLA05.3– Corpus callosum agenesisLA05.4– ArrhinencephalyLA05.5– Abnormal neuronal migrationLA05.6– Encephaloclastic disordersLA05.7– Brain cystic malformationsLA05.8– ColpocephalyLA05.Y– Other specified cerebral structural developmental anomaliesLA05.Z– Cerebral structural developmental anomalies, unspecified
Sibling codes
LA00– Anencephaly or similar anomaliesLA01– CephaloceleLA02– Spina bifidaLA03– Arnold-Chiari malformation type IILA04– Congenital hydrocephalusLA06– Cerebellar structural developmental anomaliesLA07– Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral columnLA0Y– Other specified structural developmental anomalies of the nervous systemLA0Z– Structural developmental anomalies of the nervous system, unspecified
Foundation entity
Cerebral structural developmental anomalies – http://id.who.int/icd/entity/327560976
Part of: 20: Developmental anomalies