G40.309
BillableGen idiopathic epilepsy, not intractable, w/o stat epi
Generalized idiopathic epilepsy and epileptic syndromes, not intractable, without status epilepticus
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Generalized idiopathic epilepsy and epileptic syndromes NOS
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- hippocampal sclerosis (G93.81)
- mesial temporal sclerosis (G93.81)
- temporal sclerosis (G93.81)
- Todd's paralysis (G83.84)
Code Also
A second code may be required; sequencing depends on circumstances
- MERRF syndrome, if applicable (E88.42)
Also Known As / Clinical Terms
SNOMED CT
- JME - Juvenile myoclonic epilepsy6204001
- Juvenile myoclonic epilepsy6204001
- Generalised epilepsy19598007
- Generalized epilepsy19598007
- Atypical absence seizure23374007
- IGE - idiopathic generalised epilepsy36803009
- IGE - idiopathic generalized epilepsy36803009
- Idiopathic generalised epilepsy36803009
- Idiopathic generalized epilepsy36803009
- SeLNE - self-limited neonatal epilepsy38281008
- Self-limited neonatal epilepsy38281008
- Cerebromacular degeneration42012007
- Cerebromacular dystrophy42012007
- Neuronal ceroid lipofuscinosis42012007
- Pigmentary retinal lipoid neuronal heredodegeneration42012007
- CAE - childhood absence epilepsy50866000
- Childhood absence epilepsy50866000
- Hagberg-Santavouri type neuronal ceroid lipofuscinosis58258004
- Hagberg-Santavuori disease58258004
- Haltia-Santavouri type neuronal ceroid lipofuscinosis58258004
- Infantile neuronal ceroid lipofuscinosis58258004
- Neuronal ceroid lipofuscinosis infantile Finnish type58258004
- Neuronal ceroid lipofuscinosis, infantile Finnish type58258004
- Polyunsaturated acid lipidosis58258004
- Polyunsaturated fatty acid lipidosis58258004
- Santavuori disease58258004
- Absence seizure79631006
- GAS - generalised absence seizure79631006
- GAS - generalized absence seizure79631006
- Generalised non-motor seizure79631006
- Generalised onset non-motor seizure79631006
- Generalised-onset non-motor seizure79631006
- Generalized non-motor seizure79631006
- Generalized onset non-motor seizure79631006
- Generalized-onset non-motor seizure79631006
- Benign myoclonic epilepsy in infancy192990004
- MEI - myoclonic epilepsy in infancy192990004
- Myoclonic epilepsy in infancy192990004
- Benign neonatal familial convulsions230410004
- SeLFNE - self-limited familial neonatal epilepsy230410004
- Self-limited familial neonatal epilepsy230410004
- JAE - juvenile absence epilepsy230413002
- Juvenile absence epilepsy230413002
- Epilepsy with generalised tonic-clonic seizures alone230414008
- Epilepsy with generalized tonic-clonic seizures alone230414008
- GTCA - epilepsy with generalised tonic-clonic seizures alone230414008
- GTCA - epilepsy with generalized tonic-clonic seizures alone230414008
- Baltic myoclonus epilepsy230423006
- Unverricht-Lundborg disease230423006
- Unverricht-Lundborg syndrome230423006
- Fukuhara syndrome230426003
- MERRF - myoclonic epilepsy with ragged red fibers230426003
- MERRF - myoclonic epilepsy with ragged red fibres230426003
- Myoclonic epilepsy with ragged red fibers230426003
- Myoclonic epilepsy with ragged red fibres230426003
- FBTCS - focal to bilateral tonic-clonic seizure246544003
- Focal to bilateral tonic-clonic epileptic seizure246544003
- Focal to bilateral tonic-clonic seizure246544003
- Progressive myoclonic epilepsy267581004
- EEM - epilepsy with eyelid myoclonia716278005
- Epilepsy with eyelid myoclonia716278005
- Jeavons syndrome716278005
- Early-onset Lafora body disease733082001
- Progressive myoclonic epilepsy with dystonia763349002
- Progressive myoclonus epilepsy with dystonia763349002
- AMRF - action myoclonus renal failure764453009
- Action myoclonus renal failure syndrome764453009
- Myoclonus nephropathy syndrome764453009
- Progressive myoclonic epilepsy type 4764453009
- AFG3L2 (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome771469002
- AFG3L2-related spastic ataxia, myoclonic epilepsy, neuropathy syndrome771469002
- Autosomal recessive spastic ataxia type 5771469002
- Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome771469002
- PME (progressive myoclonic epilepsy) type 5783055005
- Progressive myoclonic epilepsy type 5783055005
- Progressive myoclonus epilepsy type 5783055005
- GOSR2 (golgi SNAP receptor complex member 2) related progressive myoclonus ataxia783062001
- GOSR2-related progressive myoclonus ataxia783062001
- North Sea progressive myoclonus epilepsy783062001
- PME (progressive myoclonic epilepsy) type 6783062001
- Progressive myoclonic epilepsy type 6783062001
- Progressive myoclonus epilepsy type 6783062001
- PME (progressive myoclonic epilepsy) type 3783064000
- Progressive myoclonic epilepsy due to KCTD7 deficiency783064000
- Progressive myoclonic epilepsy type 3783064000
- Progressive myoclonus epilepsy type 3783064000
- PME (progressive myoclonic epilepsy) type 8783139000
- Progressive myoclonic epilepsy due to CERS1 (ceramide synthase 1) deficiency783139000
- Progressive myoclonic epilepsy due to ceramide synthase 1 deficiency783139000
- Progressive myoclonic epilepsy type 8783139000
- Progressive myoclonus epilepsy type 8783139000
- Disorder of glomerulus due to action myoclonus renal failure syndrome1148885001
- Glomerular disease due to action myoclonus renal failure syndrome1148885001
- EPM7 - epilepsy progressive myoclonic 71208939001
- Progressive myoclonic epilepsy due to KV3.1 deficiency1208939001
- Progressive myoclonic epilepsy type 71208939001
- Progressive myoclonus epilepsy type 71208939001
- Tonic-clonic epileptic seizure1217136003
- Tonic-clonic seizure1217136003
- PME (progressive myoclonic epilepsy) type 91228857005
- Progressive myoclonic epilepsy due to LMNB2 (lamin B2) deficiency1228857005
- Progressive myoclonic epilepsy due to LMNB2 deficiency1228857005
- Progressive myoclonic epilepsy type 91228857005
- Progressive myoclonus epilepsy type 91228857005
- GGE - genetic generalised epilepsy1260407007
- GGE - genetic generalized epilepsy1260407007
- Genetic generalised epilepsy1260407007
- Genetic generalized epilepsy1260407007
UMLS
- EIGC0270850
- EPILEPSY, IDIOPATHIC GENERALIZEDC0270850
- Epilepsy, Idiopathic GeneralizedC0270850
- Generalized idiopathic epilepsy and epileptic syndromesC0270850
- Generalized idiopathic epilepsy and epileptic syndromes NOSC0270850
- IDIOPATHIC GENERALIZED EPILEPSYC0270850
- IGEC0270850
- IGE - idiopathic generalised epilepsyC0270850
- IGE - idiopathic generalized epilepsyC0270850
- Idiopathic Generalized EpilepsyC0270850
- Idiopathic generalised epilepsyC0270850
- Idiopathic generalized epilepsyC0270850
- Idiopathic generalized epilepsy (disorder)C0270850
- epilepsies generalised idiopathicC0270850
- epilepsy generalized primaryC0270850
- idiopathic generalized epilepsyC0270850
- primary generalized epilepsyC0270850
- Gen idiopathic epilepsy, not intractable, w/o stat epiC2875106
- Generalized idiopathic epilepsy and epileptic syndromes, not intractable, without status epilepticusC2875106
Frequently Asked Questions
What is the ICD-10 code for gen idiopathic epilepsy, not intractable, w/o stat epi?
The ICD-10-CM code for gen idiopathic epilepsy, not intractable, w/o stat epi is G40.309. The full clinical description is "Generalized idiopathic epilepsy and epileptic syndromes, not intractable, without status epilepticus". G40.309 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G40.309 mean?
ICD-10-CM code G40.309 represents "Generalized idiopathic epilepsy and epileptic syndromes, not intractable, without status epilepticus". It is classified under Chapter 6: Diseases of the Nervous System and is a billable/specific code that can be used on a claim.
Is G40.309 a billable code?
Yes, G40.309 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G40.309 in?
G40.309 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What codes cannot be used with G40.309?
G40.309 has Excludes1 notes indicating codes that cannot be used together with it, including: conversion disorder with seizures (F44.5); convulsions NOS (R56.9); post traumatic seizures (R56.1); and 2 more.
What SNOMED CT codes does G40.309 map to?
G40.309 maps to 31 SNOMED CT concepts: 771469002, 764453009, 79631006, 23374007, 230423006, and 26 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G40.309?
G40.309 is linked to 2 UMLS Concept Unique Identifiers: C0270850, C2875106. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.