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 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)
Also Known As / Clinical Terms
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
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.
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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.