G31.0
Non-billableFrontotemporal dementia
Frontotemporal dementia
This is a header/category code. For billing purposes, use a more specific child code from the list below.
Coding Notes
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
Child Codes (2)
Related Codes(4)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(91)
UMLS
- Complex, Disinhibition-Dementia-Parkinsonism-AmyotrophyC0338451
- Complex, Disinhibition-Dementia-Parkinsonism-AmytrophyC0338451
- Complices, Disinhibition-Dementia-Parkinsonism-AmyotrophyC0338451
- Complices, Disinhibition-Dementia-Parkinsonism-AmytrophyC0338451
- DDPACC0338451
- DEMENTIA, FRONTOTEMPORALC0338451
- DEMENTIA, FRONTOTEMPORAL, WITH PARKINSONISMC0338451
- DISINHIBITION-DEMENTIA-PARKINSONISM-AMYOTROPHY COMPLEXC0338451
- Dementia, FrontotemporalC0338451
- Dementia, Frontotemporal LobeC0338451
- Dementia, Frontotemporal Lobe (FLDEM)C0338451
- Dementia, Frontotemporal, with ParkinsonismC0338451
- Dementia, GRN-Related FrontotemporalC0338451
- Dementia, Hereditary Dysphasic DisinhibitionC0338451
- Dementia, Ubiquitin-Positive FrontotemporalC0338451
- Dementias, FrontotemporalC0338451
- Dementias, Frontotemporal LobeC0338451
- Dementias, Frontotemporal Lobe (FLDEM)C0338451
- Dementias, GRN-Related FrontotemporalC0338451
- Dementias, Ubiquitin-Positive FrontotemporalC0338451
- Disease, Familial Pick'sC0338451
- Disease, Wilhelmsen-LynchC0338451
- Diseases, Familial Pick'sC0338451
- Diseases, Wilhelmsen-LynchC0338451
- Disinhibition Dementia Parkinsonism Amyotrophy ComplexC0338451
- Disinhibition Dementia Parkinsonism Amytrophy ComplexC0338451
- Disinhibition-Dementia-Parkinsonism-Amyotrophy ComplexC0338451
- Disinhibition-Dementia-Parkinsonism-Amyotrophy ComplicesC0338451
- Disinhibition-Dementia-Parkinsonism-Amytrophy ComplexC0338451
- Disinhibition-Dementia-Parkinsonism-Amytrophy ComplicesC0338451
- FLDEMC0338451
- FRONTOTEMPORAL DEMENTIA 1C0338451
- FRONTOTEMPORAL DEMENTIA WITH PARKINSONISMC0338451
- FRONTOTEMPORAL LOBAR DEGENERATION WITH TAU INCLUSIONSC0338451
- FRONTOTEMPORAL LOBE DEMENTIAC0338451
- FTD-GRNC0338451
- FTD-PGRNC0338451
- FTD1C0338451
- FTDP-17C0338451
- FTDP17C0338451
- FTLD WITH TAU INCLUSIONSC0338451
- FTLD with TDP 43 PathologyC0338451
- FTLD with TDP-43 PathologyC0338451
- FTLD with TDP-43 pathologyC0338451
- FTLD-17 GRNC0338451
- FTLD-TDPC0338451
- Familial Pick DiseaseC0338451
- Familial Pick's DiseaseC0338451
- Familial Pick's DiseasesC0338451
- Familial Picks DiseaseC0338451
- Frontotemporal DementiaC0338451
- Frontotemporal Dementia with ParkinsonismC0338451
- Frontotemporal Dementia with Parkinsonism 17C0338451
- Frontotemporal Dementia with Parkinsonism-17C0338451
- Frontotemporal Dementia, GRN-RelatedC0338451
- Frontotemporal Dementia, Ubiquitin PositiveC0338451
- Frontotemporal Dementia, Ubiquitin-PositiveC0338451
- Frontotemporal DementiasC0338451
- Frontotemporal Dementias, GRN-RelatedC0338451
- Frontotemporal Dementias, Ubiquitin-PositiveC0338451
- Frontotemporal Lobar Degeneration With Ubiquitin Positive InclusionsC0338451
- Frontotemporal Lobar Degeneration With Ubiquitin-Positive InclusionsC0338451
- Frontotemporal Lobe DementiaC0338451
- Frontotemporal Lobe Dementia (FLDEM)C0338451
- Frontotemporal Lobe DementiasC0338451
- Frontotemporal Lobe Dementias (FLDEM)C0338451
- Frontotemporal dementiaC0338451
- Frontotemporal dementia (disorder)C0338451
- GRN Related Frontotemporal DementiaC0338451
- GRN-Related Frontotemporal DementiaC0338451
- GRN-Related Frontotemporal DementiasC0338451
- HDDD1C0338451
- HDDD2C0338451
- Hereditary Dysphasic Disinhibition DementiaC0338451
- Lobe Dementia, FrontotemporalC0338451
- Lobe Dementias, FrontotemporalC0338451
- MSTDC0338451
- MULTIPLE SYSTEM TAUOPATHY WITH PRESENILE DEMENTIAC0338451
- Multiple System Tauopathy with Presenile DementiaC0338451
- Pick's Disease, FamilialC0338451
- Pick's Diseases, FamilialC0338451
- Ubiquitin-Positive Frontotemporal DementiaC0338451
- Ubiquitin-Positive Frontotemporal DementiasC0338451
- WILHELMSEN-LYNCH DISEASEC0338451
- WLDC0338451
- Wilhelmsen Lynch DiseaseC0338451
- Wilhelmsen-Lynch DiseaseC0338451
- Wilhelmsen-Lynch DiseasesC0338451
- Wilhelmsen-Lynch diseaseC0338451
- dementia frontotemporalC0338451
- frontotemporal dementiaC0338451
Frequently Asked Questions
What is the ICD-10 code for frontotemporal dementia?
The ICD-10-CM code for frontotemporal dementia is G31.0. The full clinical description is "Frontotemporal dementia". G31.0 is a non-billable header code. Use a more specific child code for billing purposes.
What does ICD-10 code G31.0 mean?
ICD-10-CM code G31.0 represents “Frontotemporal dementia”. It is classified under Chapter 6: Diseases of the Nervous System and is a non-billable header code. Use a more specific child code for billing purposes.
Is G31.0 a billable code?
No, G31.0 is a non-billable header code. You need to use one of its more specific child codes for billing. There are 2 child codes under G31.0.
What chapter is G31.0 in?
G31.0 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What are the subcategories under G31.0?
G31.0 has 2 child codes, including: G31.01 (Pick's disease), G31.09 (Other frontotemporal neurocognitive disorder).
Are additional codes required with G31.0?
Yes, when using G31.0, 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 are the UMLS CUIs for G31.0?
G31.0 is linked to 1 UMLS Concept Unique Identifier: C0338451. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G31.0 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like frontotemporal dementia 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 G31.0?
G31.0 maps to the ICD-11 code: 8E7Y (Other specified diseases of the nervous system).
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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.