F02.80

Billable

Dem in oth dis classd elswhr,unsp sev,w/o beh/psych/mood/anx

Dementia in other diseases classified elsewhere, unspecified severity, without behavioral disturbance, psychotic disturbance, mood disturbance, and anxiety

Status

Billable / Specific

Chapter

5: Mental, Behavioral and Neurodevelopmental Disorders

Block

F01-F09

Parent Code

F02.8

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

Dementia in other diseases classified elsewhere NOS
Major neurocognitive disorder in other diseases classified elsewhere NOS

Includes

Conditions included under this code

disorders of psychological development
Major neurocognitive disorder in other diseases classified elsewhere

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

•mild neurocognitive disorder due to known physiological condition with or without behavioral disturbanceF06.7

Excludes 2

Conditions not included here, but the patient may have both

Code First

The underlying condition must be sequenced before this code

Related Codes(4)

F02.81

Dem in other dis classd elswhr, unsp sev, with beh distrb

F02.82

Dem in other dis classd elswhr, unsp sev, with psych distrb

Billable F02.83

Dem in other dis classd elswhr, unsp sev, with mood distrb

Billable F02.84

Dem in other dis classd elswhr, unsp severity, with anxiety

Billable

Also Known As / Clinical Terms(499)

SNOMED CT

UMLS

Clinical Terms

Dementia due to celiac disease
Dementia due to polyarteritis nodosa
Dementia due to thiamine deficiency
Dementia due to renal failure
Dementia due to autoimmune encephalitis
Amyotrophic lateral sclerosis with dementia
Dementia of the Alzheimer's type, with early onset, with depressive mood
Primary degenerative dementia of the Alzheimer type, early onset
Dementia due to classical neurodegeneration with brain iron accumulation type 1
Dementia with AIDS (acquired immunodeficiency syndrome)
Dementia due to classical pantothenate kinase associated neurodegeneration
Dementia in remission
Delusions in Alzheimers disease
Myopathy with cytoplasmic inclusions
PRKAR1B-related neurodegenerative dementia with intermediate filaments
Presenile dementia, Alzheimer's type
Right temporal lobar atrophy
Dementia with acquired immunodeficiency syndrome
Dementia due to chronic intracranial subdural hematoma
Right temporal atrophy variant frontotemporal dementia
Dementia due to Wilson's disease
Dementia due to chromosomal anomaly
Dementia of the Alzheimers type with early onset
Presenile dementia co-occurrent with human immunodeficiency virus infection
Dementia due to fatal familial insomnia
Dementia due to hypertensive encephalopathy
Dementia due to systemic lupus erythematosus
Dementia due to primary malignant neoplasm of brain
Behavioural variant of frontotemporal dementia
Dementia due to acquired hypothyroidism
Dementia due to hepatolenticular degeneration
Primary degenerative dementia of the Alzheimer type, senile onset
Primary degenerative dementia of the Alzheimer type, senile onset, with depression
Dementia due to Gerstmann Straussler Scheinker syndrome
Diffuse Lewy body disease with spongiform cortical change
Dialysis dementia
Dementia due to chronic intracranial subdural haematoma
Dementia due to Parkinsons disease
Dementia due to Lyme disease
Acquired immune deficiency syndrome dementia complex
Dementia due to intracerebral hypertensive haemorrhage
Dementia due to herpes encephalitis
Dementia due to progressive subcortical gliosis
Early onset dementia due to Lewy body disease
Dementia due to chronic subdural haematoma
Dementia due to Pick disease
Dementia due to hepatic failure
Dementia due to Pick's disease
Dementia due to Creutzfeldt-Jakob disease
Dementia of the Alzheimers type, late onset
Logopenic progressive aphasia
Dementia due to infectious disease
Frontotemporal dementia due to FUS mutation
Dementia of the Alzheimer's type, with early onset, with delusions
Dementia due to haemorrhagic cerebral infarction due to hypertension
Alzheimer's disease
AD - Alzheimer's disease
Dementia due to metastatic malignant neoplasm of brain
Encephalopathy due to cobalamin deficiency
Lytico Bodig disease
SDLT - senile dementia of Lewy body type
Dementia due to niacin deficiency
Senile dementia with depression
Frontotemporal dementia due to VCP mutation
Dementia due to Behcet's syndrome
Dementia due to leukodystrophy
Hereditary dysphasic disinhibition dementia
AIDS (acquired immunodeficiency syndrome) dementia complex
LBD - Lewy body disease
Pagetoid amyotrophic lateral sclerosis
Dementia due to Hashimoto encephalopathy
Familial Pick's disease
MSTD - familial multiple system tauopathy with presenile dementia
Dementia due to classical pigmentary pallidal degeneration
Delusions in Alzheimer's disease
Alzheimer's disease with delirium
Epilepsy co-occurrent and due to dementia
Lewy body disease
ADC - Acquired immune deficiency syndrome dementia complex
Alzheimer's disease with delusions
Dementia due to celiac sprue
Dementia due to atypical pigmentary pallidal degeneration
Dementia due to hemorrhagic cerebral infarction due to hypertension
Organic dementia with acquired immunodeficiency syndrome
Dementia due to nutritional deficiency disorder
Dementia associated with neurosyphilis
Autosomal dominant Alzheimer disease with mutation of amyloid precursor protein
Non-familial Alzheimer disease of early onset
Dementia associated with normal pressure hydrocephalus
Dementia of the Alzheimer's type, with late onset, uncomplicated
CLBD - Cortical Lewy body disease
Dementia due to variant Creutzfeldt-Jakob disease
Dementia due to metabolic abnormality
Dementia due to atypical pantothenate kinase associated neurodegeneration
Familial multiple system tauopathy
Autosomal dominant Alzheimer disease due to mutation of presenilin 1
Dementia due to subacute sclerosing panencephalitis
Encephalopathy with acquired immunodeficiency syndrome
Presenile dementia with AIDS (acquired immunodeficiency syndrome)
Dementia due to intestinal lipodystrophy
Encephalopathy with AIDS (acquired immunodeficiency syndrome)
Primary degenerative dementia of the Alzheimer type, presenile onset, with depression
Alzheimer disease
Dementia associated with multiple sclerosis
SDAT - Senile dementia, Alzheimer's type
Dementia associated with viral encephalitis
Encephalopathy due to vitamin B12 deficiency
Dementia due to Lewy body disease
Dementia due to folic acid deficiency
Frontotemporal dementia due to chromosome 9 open reading frame 72 mutation
Familial Alzheimer disease of late onset
Alzheimers dementia, late onset, with depressive mood
Dementia due to kuru
Behavioral variant of frontotemporal dementia
Delusions in Alzheimer disease
Dementia due to pellagra
Major neurocognitive disorder in other diseases classified elsewhere
Dementia due to cobalamin deficiency
Non-familial Alzheimer's disease of late onset
Major neurocognitive disorder in other diseases classified elsewhere NOS
Dementia due to disorder of central nervous system
Dementia of the Alzheimer's type, with early onset, uncomplicated
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein
Dementia due to chronic subdural hematoma
Primary degenerative dementia of the Alzheimer type, presenile onset in remission
Dementia in Alzheimer's disease with early onset
Dementia of the Alzheimer's type, with late onset, with depressive mood
Autosomal dominant Alzheimer disease due to mutation of presenilin 2
Dementia due to Behcet syndrome
Dementia due to iron deficiency
Autosomal dominant Alzheimer disease with mutation of presenilin 2
Dementia due to trypanosomiasis
Primary degenerative dementia of the Alzheimer type, presenile onset, with delusions
Dementia due to Behcet's disease
Dementia co-occurrent and due to Pick's disease
Dementia due to Whipple's disease
Progressive non-fluent aphasia
Epilepsy with dementia
Dementia in Alzheimer's disease with late onset
Frontotemporal lobar degeneration
Dementia in Parkinsons disease
Primary degenerative dementia of the Alzheimer type, presenile onset
Cerebral degeneration presenting primarily with dementia
Dementia due to hypercalcaemia
Dialysis encephalopathy syndrome
Dementia due to Rett syndrome
Dementia due to obstructive hydrocephalus
Dementia co-occurrent and due to neurocysticercosis
Dementia due to rheumatological disease
Amyotrophic lateral sclerosis plus syndrome
Dementia due to nutritional deficiency
Dementia due to neurodegeneration with brain iron accumulation type 1
Alzheimer's disease with early onset
Dementia in Alzheimer's disease - type 1
Diffuse Lewy body disease
Dialysis encephalopathy
Late onset dementia due to Lewy body disease
Dementia due to Wilson disease
Amyotrophic lateral sclerosis with frontotemporal dementia
Frontotemporal dementia due to TARDBP mutation
Dementia due to steroid-responsive encephalopathy associated with autoimmune thyroiditis
Dementia due to vitamin E deficiency
Dementia due to paraneoplastic encephalitis
Frontotemporal dementia due to C9orf72 mutation
Wilhelmsen-Lynch disease
Dementia associated with another disease
Encephalopathy due to folate deficiency
Frontotemporal dementia due to valosin containing protein mutation
Dementia co-occurrent with human immunodeficiency virus infection
Dementia due to familial Creutzfeldt-Jakob disease
Dementia due to intracerebral hypertensive hemorrhage
Non-familial Alzheimer disease of late onset
Pagetoid neuroskeletal syndrome
GRN-related frontotemporal dementia
Neuropsychiatric disorder due to systemic lupus erythematosus
Familial Alzheimer's disease of early onset
Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
Parkinsonism co-occurrent with dementia of Guadeloupe
Primary degenerative dementia of the Alzheimer type, senile onset, uncomplicated
Amyotrophic lateral sclerosis, parkinsonism, dementia complex
Cortical Lewy body disease
Alzheimer's disease with late onset
Dementia due to metastatic malignant neoplasm to brain
Primary degenerative dementia of the Alzheimer type, presenile onset, uncomplicated
Senile Lewy body dementia
Dementia due to hypercalcemia
Disinhibition-dementia-parkinsonism-amytrophy complex
Primary progressive non fluent aphasia
Dementia due to inflammatory disorder of musculoskeletal system
Alzheimer dementia
Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula
Dementia due to prion disease
Guam disease
Senile dementia with depressive or paranoid features
Familial multiple system deposition of tau protein
Dementia in Alzheimer's disease - type 2
Dementia due to Picks disease
Muscular dystrophy limb-girdle with Paget disease of bone
Primary degenerative dementia of the Alzheimer type, senile onset in remission
Familial Alzheimer disease of early onset
Dementia associated with cerebral anoxia
FTDP-17 - Frontotemporal dementia with parkinsonism 17
Primary degenerative dementia of the Alzheimer type, late onset
PDALS (parkinsonism, dementia, amyotrophic lateral sclerosis) complex
Amyotrophic lateral sclerosis, parkinsonism, dementia of Guam syndrome
Dementia due to Creutzfeldt Jakob disease
Dementia due to genetic disease
Organic dementia with AIDS (acquired immunodeficiency syndrome)
Dementia due to fragile X syndrome
Protein kinase cAMP-dependent type I regulatory subunit beta-related neurodegenerative dementia with intermediate filaments
Dementia due to deficiency of folic acid
Dementia due to Behcet disease
Non-familial Alzheimer's disease of early onset
Dementia due to multiple system atrophy
Senile dementia of the Lewy body type
Dementia associated with Parkinson's Disease
Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea
Alzheimer disease with psychosis
Dementia due to leucodystrophy
Epileptic dementia
Frontotemporal dementia with parkinsonism-17
Dementia due to coeliac sprue
Dementia due to vitamin B12 deficiency
Dementia due to metastatic brain neoplasm
Dementia due to Rett's syndrome
Alzheimer's disease with psychosis
Lower motor neuron degeneration with Paget-like bone disease
Presenile dementia with depression
Dementia associated with cerebral lipidosis
Disorder of autonomic nervous system due to senile dementia of Lewy body type
Dementia due to iatrogenic Creutzfeldt-Jakob disease
Progressive aphasia
DLBD - Diffuse Lewy body disease
Familial Alzheimer's disease of late onset
Dementia in other diseases classified elsewhere NOS
Dementia associated with Parkinson Disease
Autosomal dominant Alzheimer disease with mutation of presenilin 1
IBMPFD - Inclusion body myopathy with early onset Paget disease and frontotemporal dementia
Acquired immune deficiency syndrome-related dementia
Dementia due to Parkinson's disease
Parkinsonism with dementia of Guadeloupe
Dementia due to Whipple disease
Dementia due to Parkinson disease
Alzheimers dementia, early onset, with depressed mood
Presenile dementia with acquired immunodeficiency syndrome
Dementia due to coeliac disease
Dementia due to sporadic Creutzfeldt-Jakob disease
Dementia due to neurofilament inclusion body disease

Frequently Asked Questions

What is the ICD-10 code for dem in oth dis classd elswhr,unsp sev,w/o beh/psych/mood/anx?

The ICD-10-CM code for dem in oth dis classd elswhr,unsp sev,w/o beh/psych/mood/anx is F02.80. The full clinical description is "Dementia in other diseases classified elsewhere, unspecified severity, without behavioral disturbance, psychotic disturbance, mood disturbance, and anxiety". F02.80 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code F02.80 mean?

ICD-10-CM code F02.80 represents “Dementia in other diseases classified elsewhere, unspecified severity, without behavioral disturbance, psychotic disturbance, mood disturbance, and anxiety”. It is classified under Chapter 5: Mental, Behavioral and Neurodevelopmental Disorders and is a billable/specific code that can be used on a claim.

Is F02.80 a billable code?

Yes, F02.80 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is F02.80 in?

F02.80 is in Chapter 5: Mental, Behavioral and Neurodevelopmental Disorders (codes F01-F99).

What codes cannot be used with F02.80?

F02.80 has Excludes1 notes indicating codes that cannot be used together with it, including: mild neurocognitive disorder due to known physiological condition with or without behavioral disturbance (F06.7-).

What SNOMED CT codes does F02.80 map to?

F02.80 maps to 129 SNOMED CT concepts: 26929004, 421529006, 1259128002, 142011000119109, 141991000119109, and 124 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for F02.80?

F02.80 is linked to 3 UMLS Concept Unique Identifiers: C5674930, C0349079, C4268197. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does F02.80 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like dem in oth dis classd elswhr,unsp sev,w/o beh/psych/mood/anx 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 F02.80?

There is no direct ICD-11 mapping available for F02.80 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.