G40.201 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, with status epilepticusBillable ICD-10-CM code, FY2026. Acts as a Complication or Comorbidity (CC) as a secondary diagnosis.
Defines the logic of DRG(s) 023 in MDC 01.
345.40 Localization-related (focal) (partial) epilepsy and epileptic syndromes with complex partial seizures, without mention of intractable epilepsy (approximate)G40.0 Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset ("adult onset localization-related epilepsy (G40.1-, G40.2-)")E20.810 Autosomal dominant hypocalcemia ("seizure disorder (G40.-, R56.9)")F02 Dementia in other diseases classified elsewhere ("epilepsy and recurrent seizures (G40.-)")F44.0 Dissociative amnesia ("postictal amnesia in epilepsy (G40.-)")F44.1 Dissociative fugue ("postictal fugue in epilepsy (G40.-)")F78.A1 SYNGAP1-related intellectual disability ("epilepsy and recurrent seizures (G40.-)")G04.8 Other encephalitis, myelitis and encephalomyelitis ("any associated seizure (G40.-, R56.9)")G25.3 Myoclonus ("myoclonic epilepsy (G40.-)")G40.5 Epileptic seizures related to external causes (", if applicable, associated epilepsy and recurrent seizures (G40.-)")G43.1 Migraine with aura ("any associated seizure (G40.-, R56.9)")G93.45 Developmental and epileptic encephalopathy ("epilepsy, by specific type (G40.-)")I67.850 Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy ("epilepsy (G40.-)")Q87.85 MED13L syndrome ("epilepsy and recurrent seizures (G40.-)")Q87.87 Hao-Fountain Syndrome ("epilepsy, by specific type (G40.-)")Q93.52 Phelan-McDermid syndrome ("epilepsy and recurrent seizures (G40.-)")QA0 Neurodevelopmental disorders related to specific genetic pathogenic variants ("epilepsy, by specific type (G40.-)")R56 Convulsions, not elsewhere classified ("epileptic convulsions and seizures (G40.-)")R56.1 Post traumatic seizures ("post traumatic epilepsy (G40.-)")Z15.1 Genetic susceptibility to epilepsy and neurodevelopmental disorders ("epilepsy, by specific type (G40.-)")G40.11 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractableG40.111 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, with status epilepticusG40.119 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, without status epilepticusG40.2 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizuresG40.20 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractableG40.201 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, with status epilepticus (this code)G40.209 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticusG40.21 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractableG40.211 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, with status epilepticusG40.219 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, without status epilepticusG40.3 Generalized idiopathic epilepsy and epileptic syndromes