G40.802
BillableOther epilepsy, not intractable, without status epilepticus
Other epilepsy, not intractable, without status epilepticus
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Other epilepsy NOS
- Other epilepsy without intractability without status epilepticus
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
Related Codes(3)
Also Known As / Clinical Terms(196)
SNOMED CT
- Focal onset sensory epileptic seizure with visual symptoms14521008
- Focal onset visual seizure14521008
- Focal visual seizure14521008
- Focal-onset sensory epileptic seizure with visual symptoms14521008
- Musicogenic epilepsy16873003
- Musicogenic seizure16873003
- Visual epilepsy39194005
- Anoxic seizure41510006
- Epilepsy associated with specific stimuli79745005
- Reflex epilepsy79745005
- Sensory-induced epilepsy79745005
- Focal olfactory seizure87095001
- Focal onset olfactory seizure87095001
- Focal onset sensory epileptic seizure with olfactory symptoms87095001
- Focal-onset sensory epileptic seizure with olfactory symptoms87095001
- Epilepsy only in relation to photic stimulation95208000
- Photic epilepsy95208000
- Photogenic epilepsy95208000
- Photosensitive epilepsy95208000
- Pure photosensitive epilepsy95208000
- Television epilepsy95208000
- Amelocerebrohypohidrotic syndrome109478007
- Epilepsy, dementia and amelogenesis imperfecta109478007
- Epilepsy, mental deterioration and yellow teeth109478007
- Kohlschutter syndrome109478007
- Kohlschutter's syndrome109478007
- Kohlschütter Tönz syndrome109478007
- Visual reflex epilepsy193010006
- Cursive (running) epilepsy193021002
- Cursive epilepsy193021002
- Running epilepsy193021002
- Situation-related seizures230431001
- LKS - Landau-Kleffner syndrome230438007
- Landau-Kleffner syndrome230438007
- ESSS - Epilepsy with continuous spike wave during slow-wave sleep230439004
- Electrical status epilepticus of slow-wave sleep230439004
- Epilepsy with continuous spike wave during slow-wave sleep230439004
- Secondary reading epilepsy230440002
- Catamenial epilepsy230444006
- Menstrual epilepsy230444006
- Writing epilepsy230448009
- Eating epilepsy230450001
- Toothbrushing epilepsy230452009
- Decision-making epilepsy230453004
- Aquagenic epilepsy230454005
- Bathing epilepsy230454005
- Immersion-related epilepsy230454005
- Disorder of beta and omega amino acid metabolism237940008
- Developmental aphasia268673009
- Stress-induced epilepsy413101007
- Anoxic epileptic seizure438156004
- EE - epileptic encephalopathy723125008
- Epileptic encephalopathy723125008
- P5PD developmental and epileptic encephalopathy724576005
- P5PD-DEE - pyridoxamine 5-phosphate deficiency developmental and epileptic encephalopathy724576005
- PNPO-DEE - pyridoxamine 5-phosphate oxidase developmental and epileptic encephalopathy724576005
- Pyridoxal 5-phosphate dependent epilepsy724576005
- Pyridoxal phosphate-responsive seizures724576005
- Pyridoxamine 5'-phosphate deficiency developmental and epileptic encephalopathy724576005
- Pyridoxamine 5-phosphate deficiency developmental and epileptic encephalopathy724576005
- FIRES - febrile infection-related epilepsy syndrome725413002
- Febrile infection related epilepsy syndrome725413002
- Febrile infection-related epilepsy syndrome725413002
- Antiquitin deficiency734434007
- PD-DEE - pyridoxine-dependent developmental and epileptic encephalopathy734434007
- Pyridoxine-dependent DEE (developmental and epileptic encephalopathy)734434007
- Pyridoxine-dependent developmental and epileptic encephalopathy734434007
- Pyridoxine-dependent epilepsy734434007
- Vitamin B6-dependent seizures734434007
- Hot water reflex epilepsy763534009
- Thinking epilepsy763622006
- Thinking seizures763622006
- Startle epilepsy763632004
- Micturition induced epilepsy763802009
- Micturition induced seizure763802009
- Orgasm induced epilepsy763827002
- Orgasm induced seizure763827002
- SCN8A developmental and epileptic encephalopathy765170001
- SCN8A-DEE - SCN8A - developmental and epileptic encephalopathy765170001
- SCN8A-DEE - sodium voltage-gated channel alpha subunit 8 developmental and epileptic encephalopathy765170001
- Sodium voltage-gated channel alpha subunit 8 developmental and epileptic encephalopathy765170001
- Audiogenic epilepsy765216006
- Audiogenic seizures765216006
- NORSE - new-onset refractory status epilepticus770758009
- New-onset refractory status epilepticus770758009
- Combined focal and generalised epilepsy1260117009
- Combined focal and generalized epilepsy1260117009
- Focal onset sensory epileptic seizure1281839006
- Focal onset sensory seizure1281839006
- Focal sensory seizure1281839006
- Focal-onset sensory epileptic seizure1281839006
- Disorder of GABA (gamma aminobutyric acid) metabolism16909721000119103
- Disorder of gamma aminobutyric acid metabolism16909721000119103
- Disorder of gamma-aminobutyric acid metabolism16909721000119103
UMLS
Clinical Terms
- LKS - Landau-Kleffner syndrome
- Other epilepsy NOS
- Pyridoxine-dependent developmental and epileptic encephalopathy
- EE - epileptic encephalopathy
- SCN8A-DEE - SCN8A - developmental and epileptic encephalopathy
- Epilepsy, mental deterioration and yellow teeth
- Anoxic seizure
- Startle epilepsy
- Disorder of GABA (gamma aminobutyric acid) metabolism
- Micturition induced epilepsy
- Focal onset sensory seizure
- Cursive epilepsy
- Focal sensory seizure
- Reflex epilepsy
- Catamenial epilepsy
- SCN8A-DEE - sodium voltage-gated channel alpha subunit 8 developmental and epileptic encephalopathy
- Focal onset sensory epileptic seizure with visual symptoms
- Visual reflex epilepsy
- Pyridoxine-dependent DEE (developmental and epileptic encephalopathy)
- Kohlschutter syndrome
- Pyridoxal phosphate-responsive seizures
- Combined focal and generalized epilepsy
- Disorder of gamma-aminobutyric acid metabolism
- Developmental aphasia
- Thinking seizures
- Running epilepsy
- Secondary reading epilepsy
- Focal-onset sensory epileptic seizure
- Other epilepsy
- Epilepsy associated with specific stimuli
- Sensory-induced epilepsy
- Kohlschutter's syndrome
- Audiogenic seizures
- Febrile infection-related epilepsy syndrome
- P5PD developmental and epileptic encephalopathy
- P5PD-DEE - pyridoxamine 5-phosphate deficiency developmental and epileptic encephalopathy
- Febrile infection related epilepsy syndrome
- Orgasm induced epilepsy
- Pyridoxine-dependent epilepsy
- Musicogenic seizure
- Amelocerebrohypohidrotic syndrome
- Anoxic epileptic seizure
- SCN8A developmental and epileptic encephalopathy
- Epilepsy with continuous spike wave during slow-wave sleep
- Bathing epilepsy
- Disorder of gamma aminobutyric acid metabolism
- Visual epilepsy
- Cursive (running) epilepsy
- Audiogenic epilepsy
- Toothbrushing epilepsy
- Focal onset sensory epileptic seizure with olfactory symptoms
- FIRES - febrile infection-related epilepsy syndrome
- Focal onset olfactory seizure
- Other epilepsy without intractability without status epilepticus
- Stress-induced epilepsy
- Eating epilepsy
- Hot water reflex epilepsy
- Epileptic encephalopathy
- PNPO-DEE - pyridoxamine 5-phosphate oxidase developmental and epileptic encephalopathy
- Aquagenic epilepsy
- NORSE - new-onset refractory status epilepticus
- Antiquitin deficiency
- Focal visual seizure
- Menstrual epilepsy
- New-onset refractory status epilepticus
- Photogenic epilepsy
- Television epilepsy
- Combined focal and generalised epilepsy
- Micturition induced seizure
- PD-DEE - pyridoxine-dependent developmental and epileptic encephalopathy
- Writing epilepsy
- Focal olfactory seizure
- Photosensitive epilepsy
- Musicogenic epilepsy
- Disorder of beta and omega amino acid metabolism
- Photic epilepsy
- Electrical status epilepticus of slow-wave sleep
- Pure photosensitive epilepsy
- Focal-onset sensory epileptic seizure with visual symptoms
- Decision-making epilepsy
- Thinking epilepsy
- Landau-Kleffner syndrome
- Immersion-related epilepsy
- Focal onset sensory epileptic seizure
- Kohlschütter Tönz syndrome
- Sodium voltage-gated channel alpha subunit 8 developmental and epileptic encephalopathy
- Vitamin B6-dependent seizures
- Epilepsy only in relation to photic stimulation
- Pyridoxamine 5'-phosphate deficiency developmental and epileptic encephalopathy
- Pyridoxal 5-phosphate dependent epilepsy
- Epilepsy, dementia and amelogenesis imperfecta
- Focal onset visual seizure
- Situation-related seizures
- Pyridoxamine 5-phosphate deficiency developmental and epileptic encephalopathy
- Orgasm induced seizure
- ESSS - Epilepsy with continuous spike wave during slow-wave sleep
- Focal-onset sensory epileptic seizure with olfactory symptoms
Frequently Asked Questions
What is the ICD-10 code for other epilepsy, not intractable, without status epilepticus?
The ICD-10-CM code for other epilepsy, not intractable, without status epilepticus is G40.802. The full clinical description is "Other epilepsy, not intractable, without status epilepticus". G40.802 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G40.802 mean?
ICD-10-CM code G40.802 represents “Other epilepsy, 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 G40.802 a billable code?
Yes, G40.802 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G40.802 in?
G40.802 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What codes cannot be used with G40.802?
G40.802 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 G40.802 map to?
G40.802 maps to 39 SNOMED CT concepts: 109478007, 438156004, 41510006, 734434007, 230454005, and 34 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G40.802?
G40.802 is linked to 3 UMLS Concept Unique Identifiers: C3263975, C0477371, C3263974. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G40.802 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other epilepsy, not intractable, without status epilepticus 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 G40.802?
There is no direct ICD-11 mapping available for G40.802 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.