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8A60.9 Epilepsy due to abnormalities of brain development International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01 Epilepsy due to disorders of cortical development encompassing a wide range of etiologies, with effects that depend on the stage of brain development. Seizure types usually reflect the topology of the malformation.
postcoordination Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has manifestation - multiple selections are allowed [select] 8A68 Types of seizures – 8A68.0 Focal unaware seizure – 8A68.1 Absence seizures, atypical – 8A68.2 Absence seizures, typical – 8A68.3 Focal aware seizure – 8A68.4 Generalised tonic-clonic seizure – 8A68.5 Generalised myoclonic seizure – 8A68.6 Generalised tonic seizure – 8A68.7 Generalised atonic seizure – 8A68.Y Other specified type of seizure – 8A68.Z Type of seizure, unspecified Has causing condition - a selection is required - multiple selections are allowed [select] LA00 Anencephaly or similar anomalies – LA00.0 Anencephaly – LA00.1 Iniencephaly – LA00.2 Acephaly – LA00.3 Amyelencephaly – LA00.Y Other specified anencephaly or similar anomalies – LA00.Z Anencephaly or similar anomalies, unspecified –– LA00.00 Craniorachischisis –– LA00.0Y Other specified anencephaly –– LA00.0Z Anencephaly, unspecified LA01 Cephalocele LA02 Spina bifida – LA02.0 Spina bifida cystica – LA02.1 Spina bifida aperta – LA02.Y Other specified spina bifida – LA02.Z Spina bifida, unspecified –– LA02.00 Myelomeningocele with hydrocephalus –– LA02.01 Myelomeningocele without hydrocephalus –– LA02.02 Myelocystocele –– LA02.0Y Other specified spina bifida cystica –– LA02.0Z Spina bifida cystica, unspecified LA03 Arnold-Chiari malformation type II LA04 Congenital hydrocephalus – LA04.0 Hydrocephalus with stenosis of the aqueduct of Sylvius – LA04.Y Other specified congenital hydrocephalus – LA04.Z Congenital hydrocephalus, unspecified LA05 Cerebral structural developmental anomalies – LA05.0 Microcephaly – LA05.1 Megalencephaly – LA05.2 Holoprosencephaly – LA05.3 Corpus callosum agenesis – LA05.4 Arrhinencephaly – LA05.5 Abnormal neuronal migration – LA05.6 Encephaloclastic disorders – LA05.7 Brain cystic malformations – LA05.8 Colpocephaly – LA05.Y Other specified cerebral structural developmental anomalies – LA05.Z Cerebral structural developmental anomalies, unspecified –– LA05.50 Polymicrogyria –– LA05.51 Cortical dysplasia –– LA05.5Y Other specified abnormal neuronal migration –– LA05.5Z Abnormal neuronal migration, unspecified –– LA05.60 Porencephaly –– LA05.61 Schizencephaly –– LA05.62 Hydranencephaly –– LA05.6Y Other specified encephaloclastic disorders –– LA05.6Z Encephaloclastic disorders, unspecified LA06 Cerebellar structural developmental anomalies – LA06.0 Dandy-Walker malformation – LA06.1 Hypoplasia or agenesis of cerebellar hemispheres – LA06.2 Focal cerebellar dysplasia – LA06.Y Other specified cerebellar structural developmental anomalies – LA06.Z Cerebellar structural developmental anomalies, unspecified LA07 Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column – LA07.0 Primary tethered cord syndrome – LA07.1 Diastematomyelia – LA07.2 Amyelia – LA07.3 Primary syringomyelia or hydromyelia – LA07.4 Arnold-Chiari malformation type I – LA07.Y Other specified structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column – LA07.Z Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column, unspecified LA0Y Other specified structural developmental anomalies of the nervous system LA0Z Structural developmental anomalies of the nervous system, unspecified
synonyms Epilepsy due to abnormalities of brain development Epilepsy due to cortical dysplasia epilepsy due to neuronal migration disorders
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