Diseases

Overview

This index provides a clean navigation layer for the diseases section of NeuroWiki. It currently lists 514 published diseases pages organized into logical categories for easier navigation.

Total: 514 pages

Category Index

Category	Description
Alzheimer’s & Tauopathies	AD, tauopathies, amyloid disorders
Parkinson’s & Synucleinopathies	PD, DLB, MSA, PSP, CBS
FTD & Related	FTD, bvFTD, PPA, CBD
ALS & Motor Neuron Diseases	ALS, PLS, PMA, Kennedy’s
Prion Diseases	CJD, vCJD, FFI, GSS
Huntington’s & Movement Disorders	HD, chorea, dystonia
Cerebellar Ataxias	SCAs, Friedreich, DRPLA
Mitochondrial & Metabolic Disorders	MELAS, Leigh, LHON
Lysosomal Storage Disorders	Gaucher, Batten, Niemann-Pick
Vascular & Small Vessel Diseases	CADASIL, Binswanger, CAA
Rare Genetic Disorders	NBIA, leukodystrophies
Psychiatric & Neurological	Depression, epilepsy, TBI
Investment Landscapes	Therapeutic investment by disease

All Pages

• Alpha-Synucleinopathies Comparison Matrix

• Mitochondrial Diseases and Neurodegeneration Comparison Matrix

• Abetalipoproteinemia

• Aceruloplasminemia

• AD-PD-FTD Comparison Matrix

• Adult Polyglucosan Body Disease (APBD)

• Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia (ALSP)

• Aging-Related Tau Astrogliopathy (ARTAG)

• Aging-Related Tauopathy (PART)

• Agitation in Alzheimer’s Disease

• Alexander Disease

• Alexander Disease Genetic Variants

• Allan-Herndon-Dudley Syndrome

• Alpers-Huttenlocher Syndrome

• Alpha-Mannosidosis

• Alpha-Synucleinopathies

• ALS Progression Rate Heterogeneity

• ALS-FTD Spectrum

• Alzheimer’s Disease

• Alzheimer’s Disease Genetic Variants

• Alzheimer’s Disease vs Parkinson’s Disease Comparison

• Alzheimer’s Disease vs Parkinson’s Disease Comparison

• Amyloid-Related Imaging Abnormalities (ARIA)

• Amyotrophic Lateral Sclerosis (ALS)

• Amyotrophic Lateral Sclerosis (ALS) Genetic Variants

• Angelman Syndrome

• Anti-NMDA Receptor Encephalitis

• Anxiety Disorders

• APOE2 (Apolipoprotein E2)

• APOE3 (Apolipoprotein E3)

• APOE4 (Apolipoprotein E4)

• APP Arctic Mutation (APP Arctic)

• APP Dutch Mutation (APP Dutch)

• APP Flemish Mutation (APP Flemish)

• APP Mutations in Alzheimer’s Disease

• APP Swedish Mutation (APPswe)

• Arctosia

• Argyrophilic Grain Disease (AGD)

• Ataxia Telangiectasia (AT)

• Ataxia with Oculomotor Apraxia Type 2 (AOA2)

• Ataxia with Oculomotor Apraxia Type 2 (AOA2) Genetic Variants

• Ataxia with Vitamin E Deficiency

• ATP13A9 and Parkinson’s Disease

• Atypical Parkinsonism Genetic Variants

• Autism Spectrum Disorder

• Autism Spectrum Disorder

• Autoimmune Encephalitis

• Autonomic Dysfunction in Corticobasal Syndrome

• Batten Disease

• Becker Muscular Dystrophy

• Behavioral Variant Frontotemporal Dementia (bvFTD)

• Benign Hereditary Chorea

• Beta-Propeller Protein-Associated Neurodegeneration (BPAN)

• Binswanger Disease

• Bovine Spongiform Encephalopathy (BSE)

• Bulbar Amyotrophic Lateral Sclerosis

• Bulbar Palsy

• C9orf72 Repeat Expansion in ALS

• CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy)

• Campomelic Dysplasia

• Canavan Disease

• Cancer

• CARASIL (Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy)

• Cardiomyopathy

• CASPR2 Encephalitis

• CBD Genetic Variants

• Cell-Type Vulnerability Across 4R-Tauopathies

• Cerebellar Ataxia

• Cerebral Amyloid Angiopathy (CAA)

• Cerebral Folate Deficiency (CFD)

• Cerebral Small Vessel Disease

• Cerebrotendinous Xanthomatosis (CTX)

• Charcot-Marie-Tooth Disease

• CHARGE Syndrome

• Chorea Gravidarum

• Chorea-Acanthocytosis (ChAc)

• Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

• Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

• Chronic Traumatic Encephalopathy (CTE)

• Chronic Traumatic Encephalopathy (CTE)

• Chronic Wasting Disease (CWD)

• CNS Vasculitis

• Cockayne Syndrome

• Coenzyme Q10 Deficiency

• Corticobasal Degeneration (CBD)

• Corticobasal Syndrome (CBS)

• Creutzfeldt-Jakob Disease (CJD)

• Dementia Pugilistica (Boxer’s Dementia)

• Dementia With Lewy Bodies

• Dementia with Lewy Bodies (DLB)

• Dementia with Lewy Bodies vs Parkinson’s Disease Comparison

• Dementia with Lewy Bodies vs Parkinson’s Disease Comparison

• Dentatorubral-Pallidoluysian Atrophy (DRPLA)

• Depression (Major Depressive Disorder)

• Disease Classification & Relationships

• Disease Prevalence & Burden

• Disease Progression & Staging

• Disease Rankings

• Diseases Dashboard

• Diseases Overview

• Diseases Quality Rankings

• Double Cortex Syndrome

• Down Syndrome and Alzheimer’s Disease

• DRPLA (Dentatorubral-Pallidoluysian Atrophy)

• Drug-Induced Parkinsonism

• Duchenne Muscular Dystrophy

• Dystonia

• Early-Onset Alzheimer’s Disease (EOAD)

• Epidemiology of Neurodegenerative Diseases

• Epilepsy

• Essential Tremor

• Fabry Disease

• Fahr’s Disease

• Familial Creutzfeldt-Jakob Disease (fCJD)

• Familial Dysautonomia (Riley-Day Syndrome)

• Familial Fatal Insomnia (FFI)

• Familial vs Sporadic Neurodegeneration Comparison

• Familial vs Sporadic Neurodegenerative Disease Comparison

• Fatal Familial Insomnia

• Flail Arm Syndrome

• Flail Leg Syndrome

• Fragile X Syndrome

• Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS)

• Friedreich Ataxia

• Friedreich’s Ataxia

• Frontotemporal Dementia

• Frontotemporal Dementia (FTD)

• Frontotemporal Dementia (FTD) Genetic Variants

• Frontotemporal Dementia with Parkinsonism linked to Chromosome 17 (FTDP-17)

• Frontotemporal Lobar Degeneration (FTLD)

• FTD-17 (Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17)

• FTLD-ALS: Frontotemporal Lobar Degeneration with Motor Neuron Disease

• FUS Mutations in Amyotrophic Lateral Sclerosis

• Gaucher Disease

• GBA N370S

• Gender Differences in Progressive Supranuclear Palsy

• Genetics of Progressive Supranuclear Palsy

• Gerstmann-Straussler-Scheinker Syndrome (GSS)

• Gerstmann-Sträussler-Scheinker Syndrome (GSS)

• Glaucoma

• Globular Glial Tauopathy (GGT)

• Glutaric Aciduria Type I (GA1)

• GM1 Gangliosidosis

• Guam ALS-Parkinsonism-Dementia Complex (ALS-PDC)

• Guam Parkinsonism-Dementia Complex (ALS-PDC)

• Guillain-Barré Syndrome (GBS)

• Gut-First vs Brain-First Parkinson’s Disease Trajectories

• HDL3 (Hereditary Dementia Locus 3)

• Heidenhain’s Atrophy

• Hemiballismus

• Hemichorea

• Hemiparkinsonism

• Hereditary Hemochromatosis

• Hereditary Paraganglioma

• Hereditary Sensory and Autonomic Neuropathy (HSAN)

• Hereditary Spastic Paraplegia (HSP)

• Hereditary Spastic Paraplegia Type 4 (SPG4)

• Hereditary Transthyretin Amyloidosis (hATTR)

• HIV-Associated Neurocognitive Disorders (HAND)

• Homocystinuria

• HTLV-1 Associated Myelopathy (HAM) / Tropical Spastic Paraparesis (TSP)

• Hunter Syndrome (MPS II)

• Huntington Disease

• Huntington Disease-Like (HDL) Syndromes

• Huntington Disease-Like 1 (HDL1)

• Huntington Disease-Like 2 (HDL2)

• Huntington’s Disease

• Huntington’s Disease Genetic Variants

• Huntington’s Disease Genetic Variants

• Huntington’s Disease-Like 1 (HDL1)

• Huntington’s Disease-Like 2 (HDL2)

• Iatrogenic Creutzfeldt-Jakob Disease (iCJD)

• Inclusion Body Myositis (IBM)

• Infantile Neuroaxonal Dystrophy (INAD)

• Intellectual Disability

• Investment Landscape: ALS

• Investment Landscape: Alzheimer’s Disease

• Investment Landscape: Frontotemporal Dementia

• Investment Landscape: Huntington’s Disease

• Investment Landscape: Parkinson’s Disease

• Iron Deficiency Anemia

• Japanese and German Case Series in Corticobasal Degeneration

• Jervell and Lange-Nielsen Syndrome

• Juvenile Huntington’s Disease

• Kabuki Syndrome

• Kearns-Sayre Syndrome (KSS)

• Kennedy’s Disease (Spinal Bulbar Muscular Atrophy)

• Korsakoff Syndrome

• Krabbe Disease

• Kufor-Rakeb Syndrome (PARK9)

• Kufs Disease

• Kuru

• L-2-Hydroxyglutaric Aciduria (L2GA)

• Lafora Disease

• LATE (Limbic-Predominant Age-Related TDP-43 Encephalopathy)

• Leber Hereditary Optic Neuropathy (LHON)

• Leber’s Hereditary Optic Neuropathy (LHON)

• Leigh Syndrome

• Lewy Body Dementia

• Limbic Encephalitis

• Limbic-Predominant Age-Related TDP-43 Encephalopathy (LATE)

• Lissencephaly

• Logopenic Aphasia

• Logopenic Progressive Aphasia (lvPPA)

• Logopenic Variant Primary Progressive Aphasia

• Logopenic Variant Primary Progressive Aphasia (lvPPA)

• LRRK2 G2019S

• LRRK2 Gene Variants and Mutations

• Lysosomal Storage Disorders

• Machado-Joseph Disease (Spinocerebellar Ataxia Type 3)

• Manganese-Related Neurodegeneration (Manganism)

• MAPT Gene Variants and Mutations

• Megalencephalic Leukodystrophy

• MELAS Syndrome (Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes)

• Menkes Disease

• Metachromatic Leukodystrophy (MLD)

• Microcephaly

• Migraine

• Mild Cognitive Impairment (MCI)

• Miller-Dieker Syndrome

• Minamata Disease

• Mitochondrial Membrane Protein-Associated Neurodegeneration (MPAN)

• Mitochondrial Myopathy

• Mixed Dementia

• Morquio A Syndrome

• Motor Neuron Disease (MND)

• Moyamoya Disease

• MSA Genetic Variants

• Multi-Infarct Dementia

• Multifocal Motor Neuropathy (MMN)

• Multiple Sclerosis (MS)

• Multiple System Atrophy (MSA)

• Multisystem Proteinopathy

• Muscular Dystrophy

• Myasthenia Gravis

• Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD)

• Myoclonic Epilepsy with Ragged-Red Fibers (MERRF)

• Myotonic Dystrophy

• Ménière’s Disease

• Narcolepsy

• Nasu-Hakola Disease (PLOSL)

• Neuroacanthocytosis Syndromes

• Neurodegeneration

• Neurodegeneration with Brain Iron Accumulation (NBIA)

• Neurodevelopmental Disorders

• Neuroferritinopathy

• Neuromyelitis Optica Spectrum Disorder (NMOSD)

• Neuromyelitis Optica Spectrum Disorder (NMOSD)

• Neuronal Ceroid Lipofuscinosis (NCL)

• Neuronal Intranuclear Inclusion Disease (NIID)

• Neuropsychiatric Symptoms in Progressive Supranuclear Palsy

• Neurosarcoidosis

• Niemann-Pick Disease

• Niemann-Pick Disease Type C (NPC)

• Nonfluent/Agrammatic Progressive Aphasia

• Nonketotic Hyperglycinemia

• Normal Pressure Hydrocephalus (NPH)

• Opsoclonus-Myoclonus Syndrome

• Orthostatic Hypotension

• Pantothenate Kinase-Associated Neurodegeneration (PKAN)

• Paraneoplastic Neurological Syndromes

• PARK19 (DNAJC6-Related Parkinson’s Disease)

• Parkinson Disease

• Parkinson Disease Dementia

• Parkinson’s Disease

• Parkinson’s Disease

• Parkinson’s Disease Dementia (PDD)

• Parkinson’s Disease Genetic Variants

• Parkinson’s Disease Subtypes

• Parkinson-Plus Syndromes

• Pelizaeus-Merzbacher Disease (PMD)

• Perry Syndrome

• Pheochromocytoma

• Pick’s Disease

• PLA2G6-Associated Neurodegeneration (PLAN)

• POLG-Related Mitochondrial Disorders

• Pompe Disease

• Porphyria

• Post-COVID Neurological Syndrome

• Post-Traumatic Stress Disorder

• Postencephalitic Parkinsonism

• Posterior Cortical Atrophy

• Prader-Willi Syndrome

• Preclinical Alzheimer’s Disease

• Primary Age-Related Tauopathy (PART)

• Primary Familial Brain Calcification (Fahr’s Disease)

• Primary Lateral Sclerosis (PLS)

• Primary Progressive Aphasia (PPA)

• Prion Disease

• Prion Diseases

• Prion Diseases — Comprehensive Overview

• Prodromal Alzheimer’s Disease

• Prodromal Parkinson’s Disease

• Progressive Bulbar Palsy (PBP)

• Progressive External Ophthalmoplegia

• Progressive Multifocal Leukoencephalopathy (PML)

• Progressive Muscular Atrophy (PMA)

• Progressive Myoclonic Epilepsies (PME)

• Progressive Myoclonus Epilepsy

• Progressive Supranuclear Palsy (PSP)

• Progressive Supranuclear Palsy - Richardson Syndrome

• PSEN1 Mutations in Alzheimer’s Disease

• PSEN2 Mutations in Alzheimer’s Disease

• PSEN2 Mutations in Alzheimer’s Disease

• Pseudobulbar Affect (PBA)

• PSP Clinical Variants

• PSP Epidemiology

• PSP Genetic Variants

• Pure Akinesia with Gait Freezing

• Pure Autonomic Failure

• Quality of Life and Caregiver Burden in Progressive Supranuclear Palsy

• Ramsay Hunt Syndrome

• Rapidly Progressive Dementias

• Refsum Disease

• REM Sleep Behavior Disorder (RBD)

• Restless Leg Syndrome (Willis-Ekbom Disease)

• Restless Legs Syndrome

• Retinitis Pigmentosa

• Rett Syndrome

• Sandhoff Disease

• Sanfilippo Syndrome

• Schizophrenia

• Seckel Syndrome

• Semantic Dementia (Semantic Variant Primary Progressive Aphasia)

• Semantic Variant Primary Progressive Aphasia

• Semantic Variant Primary Progressive Aphasia (svPPA)

• Senile Chorea

• Sex Reversal

• Shy-Drager Syndrome

• Sialidosis (Cherry-Red Spot Myoclonus Syndrome)

• Sleep Disorders in Neurodegeneration

• SNCA A53T

• SNCA Gene Variants and Mutations

• SOD1 Mutations in Amyotrophic Lateral Sclerosis

• Spinal Amyotrophic Lateral Sclerosis

• Spinal Cord Injury

• Spinal Muscular Atrophy (SMA)

• Spinocerebellar Ataxia (SCA)

• Spinocerebellar Ataxia Type 1 (SCA1)

• Spinocerebellar Ataxia Type 10

• Spinocerebellar Ataxia Type 17 (SCA17)

• Spinocerebellar Ataxia Type 2 (SCA2)

• Spinocerebellar Ataxia Type 6 (SCA6)

• Spinocerebellar Ataxia Type 7 (SCA7)

• Spinocerebellar Ataxia Type 8

• Sporadic ALS Initiation Mechanisms

• Sporadic Creutzfeldt-Jakob Disease (sCJD)

• Sporadic Fatal Insomnia

• Stargardt Disease

• Steele-Richardson-Olszewski Syndrome

• Stiff Person Syndrome (SPS)

• Stroke

• Subacute Sclerosing Panencephalitis (SSPE)

• Superficial Siderosis

• Sydenham Chorea

• TARDBP Mutations in Amyotrophic Lateral Sclerosis

• Tay-Sachs Disease

• Temporal Lobe Epilepsy

• TMEM106B Genetic Modifiers in FTD

• Tourette Syndrome

• Traumatic Brain Injury (TBI)

• TREM2 Variants in Alzheimer’s Disease

• Tuberous Sclerosis Complex

• Usher Syndrome

• Vanishing White Matter Disease (VWM)

• Variably Protease-Sensitive Prionopathy (VPSPr)

• Variant Creutzfeldt-Jakob Disease (vCJD)

• Vascular Cognitive Impairment (VCI)

• Vascular Dementia

• Vascular Parkinsonism

• Vasculitis Dementia

• VCP-Associated Multisystem Proteinopathy

• Veterinary Tauopathies: Cross-Species Insights

• Walker-Warburg Syndrome

• Wernicke Encephalopathy

• Wernicke-Korsakoff Syndrome

• Whipple Disease

• Williams Syndrome

• Wilson’s Disease

• Wolfram Syndrome

• Woodhouse-Sakati Syndrome (WSS)

• X-Linked Adrenoleukodystrophy (X-ALD)

• X-Linked Adrenoleukodystrophy (X-ALD) Genetic Variants

• X-Linked Intellectual Disability

• Zellweger Spectrum Disorders

• Zellweger Syndrome

By Category

Alzheimer’s Disease & Tauopathies

• Alpha-Synucleinopathies Comparison Matrix

• Mitochondrial Diseases and Neurodegeneration Comparison Matrix

• AD-PD-FTD Comparison Matrix

• Aging-Related Tau Astrogliopathy (ARTAG

• Aging-Related Tauopathy (PART

• Agitation in Alzheimer’s Disease

• Alzheimer’s Disease

• Alzheimer’s Disease Genetic Variants

• Alzheimer’s Disease vs Parkinson’s Disease Comparison

• Amyloid-Related Imaging Abnormalities (ARIA

• APP Mutations in Alzheimer’s Disease

• Argyrophilic Grain Disease (AGD

• Down Syndrome and Alzheimer’s Disease

• Early-Onset Alzheimer’s Disease (EOAD

• Primary Age-Related Tauopathy (PART

• TREM2 Variants in Alzheimer’s Disease

Parkinson’s Disease & Synucleinopathies

• ATP13A9 and Parkinson’s Disease

• Atypical Parkinsonism

• Atypical Parkinsonism Genetic Variants

• Corticobasal Degeneration (CBD

• Corticobasal Syndrome (CBS

• Dementia with Lewy Bodies (DLB

• Dementia with Lewy Bodies vs Parkinson’s Disease Comparison

• Drug-Induced Parkinsonism

• Gender Differences in Progressive Supranuclear Palsy

• Genetics of Progressive Supranuclear Palsy

• Guam ALS-Parkinsonism-Dementia Complex (ALS-PDC

• Guam Parkinsonism-Dementia Complex (ALS-PDC

• Gut-First vs Brain-First Parkinson’s Disease Trajectories

• Kufor-Rakeb Syndrome (PARK9

• LRRK2 G2019S

• LRRK2 Gene Variants and Mutations

• Manganese-Related Neurodegeneration (Manganism

• Multiple System Atrophy (MSA

• MSA Genetic Variants

• Parkinson Disease

• Parkinson Disease Dementia

• Parkinson’s Disease Genetic Variants

• Parkinson’s Disease Subtypes

• Parkinson-Plus Syndromes

• Postencephalitic Parkinsonism

• Progressive Supranuclear Palsy (PSP

• Progressive Supranuclear Palsy - Richardson Syndrome

• PSP Clinical Variants

• PSP Epidemiology

• PSP Genetic Variants

• Pure Akinesia with Gait Freezing

• REM Sleep Behavior Disorder (RBD

• SNCA A53T

• SNCA Gene Variants and Mutations

• Steele-Richardson-Olszewski Syndrome

• Vascular Parkinsonism

Frontotemporal Dementia & Related

• Behavioral Variant Frontotemporal Dementia (bvFTD

• CBD Genetic Variants

• Cell-Type Vulnerability Across 4R-Tauopathies

• Frontotemporal Dementia

• Frontotemporal Dementia (FTD) Genetic Variants

• Frontotemporal Dementia with Parkinsonism linked to Chromosome 17 (FTDP-17

• Frontotemporal Lobar Degeneration (FTLD

• FTD-17 (Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17

• FTLD-ALS: Frontotemporal Lobar Degeneration with Motor Neuron Disease

• Globular Glial Tauopathy (GGT

• Investment Landscape: Frontotemporal Dementia

• Logopenic Aphasia

• Logopenic Variant Primary Progressive Aphasia

• Nonfluent/Agrammatic Progressive Aphasia

• Pick’s Disease

• Primary Progressive Aphasia (PPA

• Semantic Dementia (Semantic Variant Primary Progressive Aphasia

• Semantic Variant Primary Progressive Aphasia

• TMEM106B Genetic Modifiers in FTD

ALS & Motor Neuron Diseases

• ALS Progression Rate Heterogeneity

• ALS-FTD Spectrum

• Amyotrophic Lateral Sclerosis (ALS

• Amyotrophic Lateral Sclerosis (ALS) Genetic Variants

• Bulbar Amyotrophic Lateral Sclerosis

• C9orf72 Repeat Expansion in ALS

• Flail Arm Syndrome

• Flail Leg Syndrome

• FUS Mutations in Amyotrophic Lateral Sclerosis

• Investment Landscape: ALS

• Kennedy’s Disease (Spinal Bulbar Muscular Atrophy

• Motor Neuron Disease (MND

• Primary Lateral Sclerosis (PLS

• Progressive Bulbar Palsy (PBP

• Progressive Muscular Atrophy (PMA

• Spinal Amyotrophic Lateral Sclerosis

• Sporadic ALS Initiation Mechanisms

• TARDBP Mutations in Amyotrophic Lateral Sclerosis

Prion Diseases

• Bovine Spongiform Encephalopathy (BSE

• Chronic Wasting Disease (CWD

• Creutzfeldt-Jakob Disease (CJD

• Familial Creutzfeldt-Jakob Disease (fCJD

• Fatal Familial Insomnia

• Gerstmann-Straussler-Scheinker Syndrome (GSS

• Iatrogenic Creutzfeldt-Jakob Disease (iCJD

• Kuru

• Sporadic Creutzfeldt-Jakob Disease (sCJD

• Sporadic Fatal Insomnia

• Variant Creutzfeldt-Jakob Disease (vCJD

• Variably Protease-Sensitive Prionopathy (VPSPr

Huntington’s Disease & Movement Disorders

• Benign Hereditary Chorea

• Chorea Gravidarum

• Chorea-Acanthocytosis (ChAc

• Dentatorubral-Pallidoluysian Atrophy (DRPLA

• Dystonia

• Hemiballismus

• Hemichorea

• Hereditary Spastic Paraplegia (HSP

• Hereditary Spastic Paraplegia Type 4 (SPG4

• Huntington Disease

• Huntington Disease-Like (HDL) Syndromes

• Huntington Disease-Like 1 (HDL1

• Huntington Disease-Like 2 (HDL2

• Huntington’s Disease

• Huntington’s Disease Genetic Variants

• Investment Landscape: Huntington’s Disease

• Juvenile Huntington’s Disease

• Neuroacanthocytosis Syndromes

• Senile Chorea

• Sydenham Chorea

Cerebellar Ataxias

• Ataxia Telangiectasia (AT

• Ataxia with Oculomotor Apraxia Type 2 (AOA2

• Ataxia with Vitamin E Deficiency

• Cerebellar Ataxia

• Coenzyme Q10 Deficiency

• Friedreich Ataxia

• Friedreich’s Ataxia

• Machado-Joseph Disease (Spinocerebellar Ataxia Type 3

• Spinocerebellar Ataxia (SCA

• Spinocerebellar Ataxia Type 1 (SCA1

• Spinocerebellar Ataxia Type 10

• Spinocerebellar Ataxia Type 17 (SCA17

• Spinocerebellar Ataxia Type 2 (SCA2

• Spinocerebellar Ataxia Type 6 (SCA6

• Spinocerebellar Ataxia Type 7 (SCA7

• Spinocerebellar Ataxia Type 8

Mitochondrial & Metabolic Disorders

• Alpers-Huttenlocher Syndrome

• Cockayne Syndrome

• Kearns-Sayre Syndrome (KSS

• Leber Hereditary Optic Neuropathy (LHON

• Leber’s Hereditary Optic Neuropathy (LHON

• Leigh Syndrome

• MELAS Syndrome (Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes

• MERRF (Myoclonic Epilepsy with Ragged-Red Fibers

• Mitochondrial Myopathy

• POLG-Related Mitochondrial Disorders

• Progressive External Ophthalmoplegia

Lysosomal Storage Disorders

• Alpha-Mannosidosis

• Adult Polyglucosan Body Disease (APBD

• Batten Disease

• Canavan Disease

• Cerebrotendinous Xanthomatosis (CTX

• Fabry Disease

• Gaucher Disease

• GBA N370S

• GM1 Gangliosidosis

• Hunter Syndrome (MPS II

• Krabbe Disease

• Lysosomal Storage Disorders

• Metachromatic Leukodystrophy (MLD

• Niemann-Pick Disease

• Niemann-Pick Disease Type C (NPC

• Sandhoff Disease

• Sanfilippo Syndrome

• Tay-Sachs Disease

Vascular & Small Vessel Diseases

• Binswanger Disease

• CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

• CARASIL (Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

• Cerebral Amyloid Angiopathy (CAA

• Cerebral Small Vessel Disease

• Multi-Infarct Dementia

• Normal Pressure Hydrocephalus (NPH

• Superficial Siderosis

• Vascular Cognitive Impairment (VCI

• Vascular Dementia

• Vasculitis Dementia

Rare Genetic Neurodegenerative Disorders

• Abetalipoproteinemia

• Aceruloplasminemia

• Adult-Onset Leukoencephalopathy with Axial Spheroids and Pigmented Glia (ALSP

• Alexander Disease

• Allan-Herndon-Dudley Syndrome

• Beta-Propeller Protein-Associated Neurodegeneration (BPAN

• Cerebral Folate Deficiency (CFD

• Familial Dysautonomia (Riley-Day Syndrome

• Glutaric Aciduria Type I (GA1

• Hereditary Hemochromatosis

• Hereditary Sensory and Autonomic Neuropathy (HSAN

• Hereditary Transthyretin Amyloidosis (hATTR

• Infantile Neuroaxonal Dystrophy (INAD

• L-2-Hydroxyglutaric Aciduria (L2GA

• Lafora Disease

• Menkes Disease

• Mitochondrial Membrane Protein-Associated Neurodegeneration (MPAN

• Nasu-Hakola Disease (PLOSL

• Neuronal Ceroid Lipofuscinosis (NCL

• Neuronal Intranuclear Inclusion Disease (NIID

• Neurodegeneration with Brain Iron Accumulation (NBIA

• Neuroferritinopathy

• Pantothenate Kinase-Associated Neurodegeneration (PKAN

• Pelizaeus-Merzbacher Disease (PMD

• PLA2G6-Associated Neurodegeneration (PLAN

• Refsum Disease

• Usher Syndrome

• Vanishing White Matter Disease (VWM

• Wilson’s Disease

• Woodhouse-Sakati Syndrome (WSS

• Zellweger Syndrome

Psychiatric & Neurological Conditions

• Anxiety Disorders

• Depression (Major Depressive Disorder

• Epilepsy

• Essential Tremor

• Fragile X Syndrome

• Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS

• Intellectual Disability

• Migraine

• Multiple Sclerosis (MS

• Myasthenia Gravis

• Narcolepsy

• Neuromyelitis Optica Spectrum Disorder (NMOSD

• Paraneoplastic Neurological Syndromes

• Post-Traumatic Stress Disorder

• Schizophrenia

• Stiff Person Syndrome (SPS

• Tourette Syndrome

• Traumatic Brain Injury (TBI

Investment Landscapes

• Investment Landscape: ALS

• Investment Landscape: Alzheimer’s Disease

• Investment Landscape: Frontotemporal Dementia

• Investment Landscape: Huntington’s Disease

• Investment Landscape: Parkinson’s Disease

Related Sections

• Genes — Disease-associated genes and risk variants

• Proteins — Disease-related proteins and aggregates

• Mechanisms — Disease pathways and molecular mechanisms

• Therapeutics — Treatments and interventions

• Biomarkers — Diagnostic and disease progression markers

See Also

• Computational Tau Spreading in PSP

• NeuroWiki Home

• All Pages

• Diseases Index

• Mechanisms Index

• Therapeutics Index

• Entities Index