G31.09
BillableOther frontotemporal neurocognitive disorder
Other frontotemporal neurocognitive disorder
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Frontal dementia
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
- •code, if applicable, to identify mild neurocognitive disorders due to known physiological conditionF06.7
Related Codes(1)
Also Known As / Clinical Terms(84)
SNOMED CT
- Frontotemporal dementia230270009
- Semantic dementia230288001
- Myopathy with cytoplasmic inclusions240086009
- Frontal lobe degeneration278855005
- DFT - Dementia frontal lobe type278857002
- Dementia of frontal lobe type278857002
- CHMP2B-related frontotemporal dementia702393003
- Chromosome 3-linked frontotemporal dementia702393003
- Frontotemporal dementia with gene located on 3p11702393003
- Frontotemporal lobar degeneration702426001
- GRN-related frontotemporal dementia702426001
- Hereditary dysphasic disinhibition dementia702426001
- Disinhibition-dementia-parkinsonism-amytrophy complex702429008
- FTDP-17 - Frontotemporal dementia with parkinsonism 17702429008
- Familial Pick's disease702429008
- Frontotemporal dementia with parkinsonism-17702429008
- Wilhelmsen-Lynch disease702429008
- IBMPFD - Inclusion body myopathy with early onset Paget disease and frontotemporal dementia703544004
- Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia703544004
- Lower motor neuron degeneration with Paget-like bone disease703544004
- Muscular dystrophy limb-girdle with Paget disease of bone703544004
- Pagetoid amyotrophic lateral sclerosis703544004
- Pagetoid neuroskeletal syndrome703544004
- Right temporal atrophy variant frontotemporal dementia716667005
- Right temporal lobar atrophy716667005
- Behavioral variant of frontotemporal dementia716994006
- Behavioural variant of frontotemporal dementia716994006
- Dementia due to chromosomal anomaly722980006
- Amyotrophic lateral sclerosis plus syndrome722987009
- Amyotrophic lateral sclerosis with frontotemporal dementia1259124000
- Familial multiple system deposition of tau protein1260328002
- Familial multiple system tauopathy1260328002
- MSTD - familial multiple system tauopathy with presenile dementia1260328002
- Frontotemporal dementia due to TARDBP mutation1260352009
- Frontotemporal dementia due to VCP mutation1260353004
- Frontotemporal dementia due to valosin containing protein mutation1260353004
- Frontotemporal dementia due to C9orf72 mutation1260354005
- Frontotemporal dementia due to chromosome 9 open reading frame 72 mutation1260354005
- Frontotemporal dementia due to FUS mutation1260355006
UMLS
Clinical Terms
- Frontotemporal dementia due to VCP mutation
- Frontotemporal dementia with gene located on 3p11
- Hereditary dysphasic disinhibition dementia
- Pagetoid amyotrophic lateral sclerosis
- Frontotemporal lobar degeneration
- frontal dementia
- Familial Pick's disease
- MSTD - familial multiple system tauopathy with presenile dementia
- Frontal lobe degeneration
- Amyotrophic lateral sclerosis plus syndrome
- DFT - Dementia frontal lobe type
- Myopathy with cytoplasmic inclusions
- Right temporal lobar atrophy
- Amyotrophic lateral sclerosis with frontotemporal dementia
- Frontotemporal dementia due to TARDBP mutation
- Right temporal atrophy variant frontotemporal dementia
- Semantic dementia
- Dementia due to chromosomal anomaly
- Familial multiple system tauopathy
- Frontotemporal dementia due to C9orf72 mutation
- Wilhelmsen-Lynch disease
- Frontotemporal dementia with parkinsonism-17
- Frontotemporal dementia due to valosin containing protein mutation
- Behavioural variant of frontotemporal dementia
- CHMP2B-related frontotemporal dementia
- Pagetoid neuroskeletal syndrome
- Dementia of frontal lobe type
- GRN-related frontotemporal dementia
- Frontotemporal dementia due to chromosome 9 open reading frame 72 mutation
- Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
- Lower motor neuron degeneration with Paget-like bone disease
- dementia frontal
- Frontotemporal dementia
- Behavioral variant of frontotemporal dementia
- Disinhibition-dementia-parkinsonism-amytrophy complex
- IBMPFD - Inclusion body myopathy with early onset Paget disease and frontotemporal dementia
- Frontotemporal dementia due to FUS mutation
- Familial multiple system deposition of tau protein
- Muscular dystrophy limb-girdle with Paget disease of bone
- Chromosome 3-linked frontotemporal dementia
- FTDP-17 - Frontotemporal dementia with parkinsonism 17
Frequently Asked Questions
What is the ICD-10 code for other frontotemporal neurocognitive disorder?
The ICD-10-CM code for other frontotemporal neurocognitive disorder is G31.09. The full clinical description is "Other frontotemporal neurocognitive disorder". G31.09 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G31.09 mean?
ICD-10-CM code G31.09 represents “Other frontotemporal neurocognitive disorder”. 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 G31.09 a billable code?
Yes, G31.09 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G31.09 in?
G31.09 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
Are additional codes required with G31.09?
Yes, when using G31.09, 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-); code, if applicable, to identify mild neurocognitive disorders due to known physiological condition (F06.7-).
What SNOMED CT codes does G31.09 map to?
G31.09 maps to 19 SNOMED CT concepts: 722987009, 1259124000, 716994006, 702393003, 278857002, and 14 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G31.09?
G31.09 is linked to 2 UMLS Concept Unique Identifiers: C1260405, C5675006. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G31.09 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other frontotemporal neurocognitive disorder 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 G31.09?
There is no direct ICD-11 mapping available for G31.09 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.