G40.009
BillableLocal-rel idio epi w seiz of loc onst,not ntrct,w/o stat epi
Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, without status epilepticus
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset 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 periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations, and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
- •hippocampal sclerosisG93.81
- •mesial temporal sclerosisG93.81
- •temporal sclerosisG93.81
- •Todd's paralysisG83.84
Also Known As / Clinical Terms(154)
SNOMED CT
- SeLFE - self-limited focal epilepsy15523002
- Self-limited focal epilepsy15523002
- Benign Rolandic epilepsy44145005
- Benign epilepsy of childhood with centro-temporal spikes44145005
- Childhood epilepsy with centrotemporal spikes44145005
- SeLECTS - self-limited epilepsy with centrotemporal spikes44145005
- Self-limited epilepsy with centrotemporal spikes44145005
- TLE - Temporal lobe epilepsy193000002
- Temporal lobe epilepsy193000002
- Paroxysmal dystonia230310003
- Focal epilepsy230381009
- Localisation-related epilepsy230381009
- Localization-related epilepsy230381009
- Benign atypical partial epilepsy in childhood230384001
- Benign childhood occipital epilepsy Panayiotopoulos type230387008
- Early-onset benign childhood occipital epilepsy230387008
- Panayiotopoulos syndrome230387008
- SeLEAS - self-limited epilepsy with autonomic seizures230387008
- Self-limited epilepsy with autonomic seizures230387008
- Benign childhood occipital epilepsy, Gastaut type230388003
- COVE - childhood occipital visual epilepsy230388003
- Childhood occipital visual epilepsy230388003
- Late onset occipital epilepsy of childhood230388003
- Occipital epilepsy of childhood, Gastaut type230388003
- Primary inherited reading epilepsy230389006
- Lateral temporal lobe epilepsy230393000
- Frontal lobe epilepsy230394006
- Parietal lobe epilepsy230403005
- Occipital lobe epilepsy230404004
- Rolandic epilepsy, speech dyspraxia syndrome765093009
- Benign familial mesial temporal lobe epilepsy770405003
- FMTLE - familial mesial temporal lobe epilepsy770405003
- Familial mesial temporal lobe epilepsy770405003
- Benign occipital epilepsy770623004
- Benign occipital lobe epilepsy770623004
- Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression773421009
- Familial temporal lobe epilepsy783739005
- Autosomal dominant epilepsy with auditory features784377008
- Autosomal dominant lateral temporal lobe epilepsy784377008
- FEAF - familial epilepsy with auditory features784377008
- Familial epilepsy with auditory features784377008
- Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome1231737000
- Combined focal and generalised epilepsy1260117009
- Combined focal and generalized epilepsy1260117009
- Temporal lobe epileptic seizure1287669005
- Temporal lobe seizure1287669005
- Parietal lobe epileptic seizure1287670006
- Parietal lobe seizure1287670006
- Occipital lobe epileptic seizure1287671005
- Occipital lobe seizure1287671005
- Frontal lobe epileptic seizure1287672003
- Frontal lobe seizure1287672003
- Lateral temporal lobe epileptic seizure1287673008
- Lateral temporal lobe seizure1287673008
- Mesial temporal lobe epileptic seizure1287674002
- Mesial temporal lobe seizure1287674002
- Frontal lobe supplementary motor cortex epileptic seizure1287675001
- Supplementary motor seizure1287675001
- Frontal lobe primary motor cortex epileptic seizure1287676000
- Primary motor seizure1287676000
- SeLIE - self-limited infantile epilepsy1332157006
- Self-limited infantile epilepsy1332157006
- EAF - epilepsy with auditory features1332158001
- Epilepsy with auditory features1332158001
- SHE - sleep-related hypermotor epilepsy1332160004
- Sleep-related hyperkinetic epilepsy1332160004
- Sleep-related hypermotor epilepsy1332160004
- POLE - photosensitive occipital lobe epilepsy1335933003
- Photosensitive occipital lobe epilepsy1335933003
- Insular epilepsy1343613004
- MTLE - mesial temporal lobe epilepsy1343664003
- Mesial temporal lobe epilepsy1343664003
- Temporal lobe epilepsy with mesial temporal sclerosis5321000124109
UMLS
- Local-rel (focal) idio epilepsy w seizures of loc onsetC0475521
- Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onsetC0475521
- Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset NOSC0475521
- Local-rel idio epi w seiz of loc onst,not ntrct,w/o stat epiC2875077
- Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, without status epilepticusC2875077
Clinical Terms
- MTLE - mesial temporal lobe epilepsy
- SeLFE - self-limited focal epilepsy
- Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset
- Occipital lobe epileptic seizure
- Parietal lobe epilepsy
- TLE - Temporal lobe epilepsy
- Mesial temporal lobe epilepsy
- Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
- Occipital lobe epilepsy
- Local-rel (focal) idio epilepsy w seizures of loc onset
- POLE - photosensitive occipital lobe epilepsy
- Frontal lobe primary motor cortex epileptic seizure
- Frontal lobe epilepsy
- Sleep-related hyperkinetic epilepsy
- Mesial temporal lobe seizure
- SeLIE - self-limited infantile epilepsy
- EAF - epilepsy with auditory features
- Combined focal and generalized epilepsy
- Lateral temporal lobe epileptic seizure
- Supplementary motor seizure
- Late onset occipital epilepsy of childhood
- Lateral temporal lobe epilepsy
- Childhood occipital visual epilepsy
- Temporal lobe epileptic seizure
- Primary inherited reading epilepsy
- Parietal lobe epileptic seizure
- Sleep-related hypermotor epilepsy
- Mesial temporal lobe epileptic seizure
- Panayiotopoulos syndrome
- Occipital epilepsy of childhood, Gastaut type
- Photosensitive occipital lobe epilepsy
- Benign Rolandic epilepsy
- Self-limited epilepsy with centrotemporal spikes
- Benign occipital lobe epilepsy
- Self-limited infantile epilepsy
- Occipital lobe seizure
- Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset NOS
- Temporal lobe seizure
- SHE - sleep-related hypermotor epilepsy
- Temporal lobe epilepsy
- Self-limited epilepsy with autonomic seizures
- Insular epilepsy
- Primary motor seizure
- Focal epilepsy
- Childhood epilepsy with centrotemporal spikes
- Familial mesial temporal lobe epilepsy
- Autosomal dominant epilepsy with auditory features
- Self-limited focal epilepsy
- Lateral temporal lobe seizure
- Parietal lobe seizure
- Benign childhood occipital epilepsy, Gastaut type
- SeLEAS - self-limited epilepsy with autonomic seizures
- FEAF - familial epilepsy with auditory features
- SeLECTS - self-limited epilepsy with centrotemporal spikes
- Early-onset benign childhood occipital epilepsy
- Paroxysmal dystonia
- Localisation-related epilepsy
- Combined focal and generalised epilepsy
- Autosomal dominant lateral temporal lobe epilepsy
- FMTLE - familial mesial temporal lobe epilepsy
- Familial temporal lobe epilepsy
- COVE - childhood occipital visual epilepsy
- Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome
- Epilepsy with auditory features
- Benign occipital epilepsy
- Familial epilepsy with auditory features
- Localization-related epilepsy
- Benign atypical partial epilepsy in childhood
- Rolandic epilepsy, speech dyspraxia syndrome
- Temporal lobe epilepsy with mesial temporal sclerosis
- Benign epilepsy of childhood with centro-temporal spikes
- Frontal lobe supplementary motor cortex epileptic seizure
- Benign childhood occipital epilepsy Panayiotopoulos type
- Frontal lobe epileptic seizure
- Benign familial mesial temporal lobe epilepsy
- Frontal lobe seizure
Frequently Asked Questions
What is the ICD-10 code for local-rel idio epi w seiz of loc onst,not ntrct,w/o stat epi?
The ICD-10-CM code for local-rel idio epi w seiz of loc onst,not ntrct,w/o stat epi is G40.009. The full clinical description is "Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, without status epilepticus". G40.009 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G40.009 mean?
ICD-10-CM code G40.009 represents “Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, 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 G40.009 a billable code?
Yes, G40.009 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G40.009 in?
G40.009 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What codes cannot be used with G40.009?
G40.009 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 3 more.
What SNOMED CT codes does G40.009 map to?
G40.009 maps to 36 SNOMED CT concepts: 784377008, 44145005, 230384001, 230387008, 230388003, and 31 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G40.009?
G40.009 is linked to 2 UMLS Concept Unique Identifiers: C0475521, C2875077. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G40.009 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like local-rel idio epi w seiz of loc onst,not ntrct,w/o stat epi affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of G40.009?
There is no direct ICD-11 mapping available for G40.009 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.