Version June 2024
| Neurodegenerative dementias |
| Alzheimer disease |
| Presenilin 1 mutation |
| Presenilin 2 mutation |
| Amyloid precursor protein mutation |
| APOE ε4-associated disease |
| Down syndrome related dementia |
| Frontotemporal dementia |
| Dementia with Lewy bodies |
| Parkinson disease dementia |
| Progressive supranuclear palsy |
| Corticobasal degeneration |
| Multiple system atrophy |
| Vascular diseases |
| Vascular dementia |
| Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy |
| Cerebral amyloid angiopathy |
| Primary angiitis of the central nervous system |
| Secondary central nervous system vasculitis |
| Infectious diseases |
| Prion disease |
| HIV-associated neurocognitive disorder |
| Herpes encephalitis |
| Neurosyphilis |
| Whipple disease |
| Progressive multifocal leukoencephalopathy |
| Subacute sclerosing panencephalitis |
| Inflammatory and autoimmune diseases |
| Multiple sclerosis |
| Neurosarcoidosis |
| Paraneoplastic encephalopathy |
| Non-paraneoplastic autoimmune encephalopathy |
| Encephalopathy due to systemic autoimmune disease |
| Neurometabolic disorders |
| Mitochondrial disease |
| Late-onset lysosomal diseases |
| Adult-onset leukodystrophies |
| Adult polyglucosan body disease |
| Diffuse hereditary leukoencephalopathy with axonal spheroids |
| Adult neuronal ceroid lipofuscinosis |
| Others |
| Chronic traumatic encephalopathy |
| Alcohol-related dementia |
| Normal pressure hydrocephalus |
| Huntington disease |
| Wilson disease |
| Spinocerebellar atrophy |
| Dentatorubral pallidoluysian atrophy |
| Familial encephalopathy with neuroserpin inclusion bodies |
| Pantothenate kinase associated neurodegeneration |
| Familial idiopathic basal ganglia calcification (Fahr disease) |
| Superficial siderosis |
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