G31.82
BillableLeigh's disease
Leigh's disease
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Subacute necrotizing encephalopathy
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
- •Reye's syndromeG93.7
Use Additional Code
Additional codes that should follow this code
- •code, if applicable, for codes , , to identify:G31.0-G31.83, G31.85-G31.9
- •dementia with anxiety, A4, B4, C4)F02.84, F02, F02, F02
- •dementia with behavioral disturbance, A1-, B1-, C1-)F02.81, F02, F02, F02
- •dementia with mood disturbance, A3, B3, C3)F02.83, F02, F02, F02
- •dementia with psychotic disturbance, A2, B2, C2)F02.82, F02, F02, F02
- •dementia without behavioral disturbance, A0, B0, C0)F02.80, F02, F02, F02
- •mild neurocognitive disorder due to known physiological conditionF06.7
Related Codes(7)
G31.80Leukodystrophy, unspecified
G31.81Alpers disease
G31.83Neurocognitive disorder with Lewy bodies
G31.84Mild cognitive impairment of uncertain or unknown etiology
G31.85Corticobasal degeneration
G31.86Alexander disease
G31.89Other specified degenerative diseases of nervous system
Also Known As / Clinical Terms(133)
SNOMED CT
- Infantile necrotising encephalomyelopathy29570005
- Infantile necrotizing encephalomyelopathy29570005
- Leigh disease29570005
- Leigh syndrome29570005
- Leigh's disease29570005
- Leighs disease29570005
- SNEM - Subacute necrotising encephalomyelopathy29570005
- SNEM - Subacute necrotizing encephalomyelopathy29570005
- Subacute necrotising encephalomyelopathy29570005
- Subacute necrotising encephalopathy29570005
- Subacute necrotizing encephalomyelopathy29570005
- Subacute necrotizing encephalopathy29570005
- COX - Cytochrome C oxidase deficiency67434000
- Complex IV deficiency67434000
- Cytochrome c oxidase deficiency67434000
- Cytochrome-c oxidase deficiency67434000
- Mitochondrial complex IV deficiency67434000
- Maternally inherited Leigh disease717052002
- Maternally inherited Leigh syndrome717052002
- Maternally inherited infantile subacute necrotising encephalopathy717052002
- Maternally inherited infantile subacute necrotizing encephalopathy717052002
- Congenital lactic acidosis Saguenay-Lac-Saint-Jean type718219002
- Cytochrome C oxidase deficiency French-Canadian type718219002
- Cytochrome oxidase deficiency Saguenay-Lac-Saint-Jean type718219002
- Leigh syndrome French-Canadian type718219002
- Familial acute necrotising encephalopathy723359002
- Familial acute necrotizing encephalopathy723359002
- Recurrent acute necrotising encephalopathy723359002
- Recurrent acute necrotizing encephalopathy723359002
- Leigh syndrome due to cytochrome C oxidase deficiency1187520001
- Dystonia due to Leigh syndrome1187533007
UMLS
- Disease, Leigh'sC0023264
- ENCEPH SUBACUTE NECROTIZINGC0023264
- Encephalomyelitides, Subacute NecrotizingC0023264
- Encephalomyelitis, Subacute NecrotizingC0023264
- Encephalomyelopathies, Subacute NecrotizingC0023264
- Encephalomyelopathy, Subacute NecrotizingC0023264
- Encephalopathies, Subacute NecrotizingC0023264
- Encephalopathy, Subacute NecrotizingC0023264
- LEIGH DISC0023264
- LEIGH SYNDROMEC0023264
- LEIGHS DISC0023264
- Leigh DiseaseC0023264
- Leigh SyndromeC0023264
- Leigh diseaseC0023264
- Leigh syndromeC0023264
- Leigh's DiseaseC0023264
- Leigh's diseaseC0023264
- Leigh's disease (disorder)C0023264
- Leighs DiseaseC0023264
- Leighs diseaseC0023264
- Necrotizing Encephalomyelitides, SubacuteC0023264
- Necrotizing Encephalomyelitis, SubacuteC0023264
- Necrotizing Encephalomyelopathies, SubacuteC0023264
- Necrotizing Encephalomyelopathy, SubacuteC0023264
- Necrotizing Encephalopathies, SubacuteC0023264
- Necrotizing Encephalopathy, SubacuteC0023264
- SNEM - Subacute necrotising encephalomyelopathyC0023264
- SNEM - Subacute necrotizing encephalomyelopathyC0023264
- SUBACUTE NECROTIZING ENCEPHC0023264
- Subacute Necrotizing EncephalomyelitidesC0023264
- Subacute Necrotizing EncephalomyelitisC0023264
- Subacute Necrotizing EncephalomyelopathiesC0023264
- Subacute Necrotizing EncephalomyelopathyC0023264
- Subacute Necrotizing EncephalopathiesC0023264
- Subacute Necrotizing EncephalopathyC0023264
- Subacute necrotising encephalomyelopathyC0023264
- Subacute necrotising encephalopathyC0023264
- Subacute necrotizing encephalomyelopathyC0023264
- Subacute necrotizing encephalopathyC0023264
- disease leighC0023264
- diseases leighsC0023264
- leigh diseaseC0023264
- leigh syndromeC0023264
- leigh's diseaseC0023264
- leighs diseaseC0023264
- leighs syndromeC0023264
- subacute necrotizing encephalomyelopathyC0023264
Clinical Terms
- SUBACUTE NECROTIZING ENCEPH
- LEIGH DIS
- leighs disease
- Encephalomyelitides, Subacute Necrotizing
- Leigh Disease
- Leigh's disease (disorder)
- Cytochrome C oxidase deficiency French-Canadian type
- LEIGHS DIS
- Leigh syndrome
- Subacute necrotising encephalopathy
- Recurrent acute necrotising encephalopathy
- Cytochrome oxidase deficiency Saguenay-Lac-Saint-Jean type
- Familial acute necrotizing encephalopathy
- Recurrent acute necrotizing encephalopathy
- leighs syndrome
- Necrotizing Encephalomyelitides, Subacute
- Necrotizing Encephalomyelopathies, Subacute
- Leigh syndrome due to cytochrome C oxidase deficiency
- Leigh syndrome French-Canadian type
- Subacute necrotising encephalomyelopathy
- Maternally inherited Leigh disease
- Maternally inherited Leigh syndrome
- Encephalopathies, Subacute Necrotizing
- Subacute Necrotizing Encephalomyelitis
- disease leigh
- Disease, Leigh's
- Necrotizing Encephalomyelitis, Subacute
- Infantile necrotizing encephalomyelopathy
- COX - Cytochrome C oxidase deficiency
- Necrotizing Encephalopathies, Subacute
- Encephalopathy, Subacute Necrotizing
- Necrotizing Encephalomyelopathy, Subacute
- Necrotizing Encephalopathy, Subacute
- Maternally inherited infantile subacute necrotizing encephalopathy
- Complex IV deficiency
- Subacute Necrotizing Encephalomyelopathy
- Subacute necrotizing encephalopathy
- Subacute Necrotizing Encephalomyelitides
- Cytochrome-c oxidase deficiency
- Maternally inherited infantile subacute necrotising encephalopathy
- Congenital lactic acidosis Saguenay-Lac-Saint-Jean type
- Infantile necrotising encephalomyelopathy
- Subacute Necrotizing Encephalomyelopathies
- Subacute Necrotizing Encephalopathies
- Encephalomyelitis, Subacute Necrotizing
- Cytochrome c oxidase deficiency
- Familial acute necrotising encephalopathy
- ENCEPH SUBACUTE NECROTIZING
- Encephalomyelopathies, Subacute Necrotizing
- diseases leighs
- Mitochondrial complex IV deficiency
- SNEM - Subacute necrotizing encephalomyelopathy
- SNEM - Subacute necrotising encephalomyelopathy
- Encephalomyelopathy, Subacute Necrotizing
- Dystonia due to Leigh syndrome
Frequently Asked Questions
What is the ICD-10 code for leigh's disease?
The ICD-10-CM code for leigh's disease is G31.82. The full clinical description is "Leigh's disease". G31.82 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G31.82 mean?
ICD-10-CM code G31.82 represents “Leigh's disease”. 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 G31.82 a billable code?
Yes, G31.82 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G31.82 in?
G31.82 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
Are additional codes required with G31.82?
Yes, when using G31.82, also report: code, if applicable, for codes G31.0-G31.83, G31.85-G31.9, to identify:; dementia with anxiety (F02.84, F02.A4, F02.B4, F02.C4); dementia with behavioral disturbance (F02.81-, F02.A1-, F02.B1-, F02.C1-); dementia with mood disturbance (F02.83, F02.A3, F02.B3, F02.C3); dementia with psychotic disturbance (F02.82, F02.A2, F02.B2, F02.C2); dementia without behavioral disturbance (F02.80, F02.A0, F02.B0, F02.C0); mild neurocognitive disorder due to known physiological condition (F06.7-).
What SNOMED CT codes does G31.82 map to?
G31.82 maps to 7 SNOMED CT concepts: 67434000, 718219002, 1187533007, 723359002, 29570005, and 2 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G31.82?
G31.82 is linked to 1 UMLS Concept Unique Identifier: C0023264. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G31.82 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like leigh's disease 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 G31.82?
There is no direct ICD-11 mapping available for G31.82 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.