| 疾病名称 |
别名 |
|
| Creutzfeldt-Jakob Disease |
|
Variant Creutzfeldt-Jakob Disease
|
CJD
|
|
Bovine Spongiform Encephalopathy
|
Vcjd
|
|
Inherited Creutzfeldt-Jakob Disease
|
Creutzfeldt-Jakob Disease, Familial
|
|
Creutzfeldt Jakob Disease
|
Creutzfeldt-Jacob Disease
|
|
Creutzfeldt Jacob Disease
|
Sporadic Creutzfeldt-Jakob Disease
|
|
Encephalopathy, Bovine Spongiform
|
Creutzfeldt-Jakob Disease, Variant, Resistance To
|
|
Creutzfeldt-Jakob Disease, Variant
|
Creutzfeldt Jacob Syndrome
|
|
Jakob-Creutzfeldt Disease
|
Subacute Spongiform Encephalopathy
|
|
Transmissible Virus Dementia
|
New Variant Of Cjd
|
|
Nv-Cjd
|
Variant Cjd
|
|
Variant Creutzfeldt-Jacob Disease
|
Sporadic Cjd
|
|
Inherited Cjd
|
Acquired Creutzfeldt-Jakob Disease
|
|
Variant Mcj
|
Encephalopathy Bovine Spongiform
|
|
Familial Creutzfeldt-Jakob Disease
|
Creutzfeldt-Jakob Syndrome
|
|
New Variant Creutzfeldt-Jakob Disease
|
Creutzfeldt-Jakob Disease, Sporadic
|
|
Acquired Cjd
|
Scjd - [Sporadic Creutzfeldt-Jakob Disease]
|
|
Idiopathic Creutzfeldt-Jakob Disease
|
Creutzfeld-Jakob Disease Nos
|
|
Vcjd - [Variant Creutzfeldt-Jakob Disease]
|
|
|
| Fatal Familial Insomnia |
|
Insomnia, Fatal Familial
|
FFI
|
|
Familial Fatal Insomnia
|
Insomnia Familial Fatal
|
|
Insomnia Fatal Familial
|
Insomnia, Fatal, Familial
|
|
Ffi - [Fatal Familial Insomnia]
|
|
|
| Gerstmann-Straussler Disease |
|
Gerstmann-Straussler-Scheinker Disease
|
Gerstmann-Straussler-Scheinker Syndrome
|
|
Prion Dementia
|
Cerebral Amyloid Angiopathy, Prnp-Related
|
|
GSD
|
Gss
|
|
Cerebellar Ataxia, Progressive Dementia, And Amyloid Deposits In Cns
|
Amyloidosis, Cerebral, With Spongiform Encephalopathy
|
|
Subacute Spongiform Encephalopathy, Gerstmann-Straussler Type
|
Encephalopathy, Subacute Spongiform, Gerstmann-Straussler Type
|
|
Amyloidosis Cerebral With Spongiform Encephalopathy
|
Cerebellar Ataxia, Progressive Dementia, And Amyloid Deposits In The Central Nervous System
|
|
Encephalopathy Subacute Spongiform Gerstmann-Straussler Type
|
Gssd
|
|
Gerstmann Straussler Scheinker Syndrome
|
Cerebral Amyloidosis With Spongiform Encephalopathy
|
|
Subacute Spongiform Encephalopathy Gerstmann-Straussler Type
|
Gluthathione Synthetase Deficiency
|
|
Gerstmann Straussler Syndrome
|
|
|
| Huntington Disease-Like 1 |
|
HDL1
|
Huntington-Like Neurodegenerative Disorder 1
|
|
Hln1
|
Huntington'S Disease-Like 1
|
|
Early-Onset Prion Disease With Prominent Psychiatric Features
|
Huntington-Like Neurodegenerative Disorder, Autosomal Dominant
|
|
Prion Disease, Early-Onset, With Prominent Psychiatric Features
|
Autosomal Dominant Huntington-Like Neurodegenerative Disorder
|
|
Huntington Disease-Like, Type 1
|
|
|
| Spongiform Encephalopathy With Neuropsychiatric Features |
|
|
| Kuru |
|
Kuru, Susceptibility To
|
Kuru Encephalopathy
|
|
Kuru Encephalitis
|
Kuru Disease
|
|
|
| Prion Disease |
|
Spongiform Encephalopathy
|
Transmissible Spongiform Encephalopathies
|
|
Prion Diseases
|
Prion Disease Pathway
|
|
Transmissible Spongiform Encephalopathy
|
Prion Induced Disorder
|
|
Prion Protein Disease
|
Inherited Human Transmissible Spongiform Encephalopathies
|
|
Prion Protein Diseases
|
Prion-Associated Disorders
|
|
Prion-Induced Disorders
|
Transmissible Dementias
|
|
Tses
|
Human Prion Disease
|
|
Tse
|
Encephalopathy, Transmissible Spongiform
|
|
Prion Disease, Susceptibility To
|
Spongiform Encephalopathies
|
|
Human Transmissible Spongiform Encephalopathies, Inherited
|
|
|
| Inherited Human Prion Disease |
|
Inherited Prion Disease
|
Familial Prion Disease
|
|
Genetic Human Prion Disease
|
|
|
| Familial Alzheimer-Like Prion Disease |
|
|
| Prp Systemic Amyloidosis |
|
Chronic Diarrhea With Hsan
|
Chronic Diarrhea With Hereditary Sensory And Autonomic Neuropathy
|
|
Prion Protein Systemic Amyloidosis
|
|
|
| Scrapie |
|
|
| Chronic Wasting Disease |
|
|
| Frontotemporal Lobar Degeneration With Tdp43 Inclusions, Grn-Related |
|
Primary Progressive Aphasia
|
Grn-Related Frontotemporal Lobar Degeneration With Tdp43 Inclusions
|
|
Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions
|
Frontotemporal Dementia, Ubiquitin-Positive
|
|
Aphasia, Primary Progressive
|
Ppa
|
|
Ftld-Tdp, Grn-Related
|
Frontotemporal Dementia With Tdp43 Inclusions, Grn-Related
|
|
Ftldu
|
Ftdu
|
|
Dementia, Hereditary Dysphasic Disinhibition
|
Hddd
|
|
Primary Progressive Aphasia Syndrome
|
Mesulam Syndrome
|
|
Ubiquitin-Positive Frontotemporal Dementia
|
UP-FTD
|
|
Tau-Negative Frontotemporal Dementia Linked To Chromosome 17
|
Aphasia Primary Progressive
|
|
Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions, Susceptibility To
|
Aphasia, Primary Progressive, Susceptibility To
|
|
Frontotemporal Dementia
|
|
|
| Dementia |
|
Dementias
|
Presenile Dementia
|
|
Alzheimer Type Dementia
|
Alzheimer Sclerosis
|
|
Alzheimer Disease Dementia
|
Alzheimer Dementia
|
|
Primary Degenerative Alzheimer Type Dementia
|
End Stage Alzheimer'S Dementia
|
|
Alzheimer'S Type Atypical Dementia
|
Alzheimer Type Presenile Dementia
|
|
Early Onset Alzheimer Dementia
|
Dementia In Alzheimer Disease Type 2
|
|
Dementia In Alzheimer Disease With Early Onset
|
Early Onset Alzheimer Type Dementia, Uncomplicated
|
|
Primary Degenerative Alzheimer Type Dementia, Early Onset
|
Primary Degenerative Alzheimer Type Dementia, Presenile Onset, Uncomplicated
|
|
Alzheimer Disease Dementia With Early Onset
|
Presenile Sclerosis
|
|
Presenile Brain Sclerosis
|
Presenile Alzheimer Brain Sclerosis
|
|
Late Onset Alzheimer Dementia
|
Dementia In Alzheimer Disease Type 1
|
|
Dementia In Alzheimer Disease With Late Onset
|
Primary Degenerative Alzheimer Type Dementia, Late Onset
|
|
Sdat - [Senile Dementia, Alzheimer Type]
|
Alzheimer Disease Dementia With Late Onset
|
|
Late Onset Alzheimer Brain Sclerosis
|
Senile Alzheimer Brain Disease
|
|
Senile Alzheimer Brain Sclerosis
|
Senile Primary Degenerative Alzheimer Type Dementia
|
|
Senile Dementia Of The Alzheimer Type
|
Arteriosclerotic Dementia
|
|
Strategic-Infarct Dementia
|
Post Stroke Dementia
|
|
Vascular Cognitive Impairment
|
Vascular Dementia
|
|
Dementia Of The Lewy Body Type
|
Dementia With Lewy Bodies
|
|
Sdlt - [Senile Dementia Of The Lewy Body Type]
|
Senile Dementia Of The Lewy Body Type
|
|
Alcohol-Related Dementia
|
Alcoholic Dementia Nos
|
|
Alcohol-Induced Dementia
|
Alcoholic Brain Syndrome
|
|
Chronic Alcoholic Brain Syndrome
|
Alcohol Dementia
|
|
Late Onset Alcoholic Psychosis
|
Residual And Late-Onset Alcohol-Induced Psychotic Disorder
|
|
Mental And Behavioural Disorders Due To Use Of Sedatives Or Hypnotics, Residual And Late-Onset Psychotic Disorder
|
Late-Onset Psychoactive Substance-Induced Psychotic Disorder
|
|
Inhalant Dementia
|
Volatile Solvents Dementia
|
|
Dementia In Paralysis Agitans
|
Pdd - [Parkinson Disease Dementia]
|
|
Dementia Syndrome Of Parkinson Disease
|
Dementia In Parkinson Disease
|
|
Parkinson Related Dementia
|
Dementia In Huntington Chorea
|
|
Hiv - [Human Immunodeficiency Virus] Dementia
|
Hiv- [Human Immunodeficiency Virus] Associated Cognitive Motor Complex
|
|
Hiv- [Human Immunodeficiency Virus] Associated Dementia Complex
|
Aids - [Acquired Immunodeficiency Syndrome] Dementia Complex
|
|
Aids Related Dementia
|
Dementia Due To Niacin Deficiency
|
|
|
| Huntington Disease |
|
Huntington'S Disease
|
Huntington Chorea
|
|
Huntington'S Chorea
|
HD
|
|
Huntington Chronic Progressive Hereditary Chorea
|
Juvenile Huntington Disease
|
|
Chronic Progressive Chorea
|
Chronic Progressive Hereditary Chorea
|
|
Hc - [Huntington Chorea]
|
Hereditary Chorea
|
|
Progressive Hereditary Chorea
|
|
|
| Encephalopathy |
|
Brain Diseases
|
Encephalopathies
|
|
Toxic Encephalopathy
|
Toxic Brain Fever
|
|
Toxic Brain Inflammation
|
Toxic Brain Stem Inflammation
|
|
Toxic Cerebral Fever
|
Toxic Cerebrospinal Fever
|
|
Toxic Cerebrospinal Inflammation
|
Encephalopathy Nec
|
|
Encephalopathy Nos
|
Encephalopathy Disease
|
|
Encephalopathy Syndrome
|
|
|
| Cerebral Amyloid Angiopathy, Cst3-Related |
|
Cerebral Amyloid Angiopathy
|
Hereditary Cerebral Hemorrhage With Amyloidosis
|
|
Hchwa
|
Hereditary Cystatin C Amyloid Angiopathy
|
|
Cerebral Amyloid Angiopathy, Familial
|
Amyloidosis, Cerebroarterial, Icelandic Type
|
|
Amyloidosis Vi
|
Cerebral Hemorrhage, Hereditary, With Amyloidosis
|
|
Cst3-Related Cerebral Amyloid Angiopathy
|
Cerebral Hemorrhage, Hereditary, With Amyloidosis, Icelandic Variant
|
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Icelandic Variant
|
Caa, Familial
|
|
Cerebral Amyloid Angiopathy, Genetic
|
Acys Amyloidosis
|
|
Cst3-Related Amyloidosis
|
Cystatin Amyloidosis
|
|
Hchwa, Icelandic Type
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Icelandic Type
|
|
Amyloidosis 6
|
AMYL6
|
|
Acys
|
Caa
|
|
Cerebral Amyloid Angiopathy Cst3-Related
|
Cerebroarterial Amyloidosis Icelandic Type
|
|
Cystatin C Amyloidosis
|
Hccaa
|
|
Hchwai
|
Hchwa-I
|
|
Hereditary Cerebral Hemorrhage With Amyloidosis Icelandic Type
|
Cerebral Amyloid Angiopathy Familial
|
|
Angiopathy, Amyloid, Cerebral, Cst3-Related
|
Hereditary Cerebral Amyloid Angiopathy, Icelandic Type
|
|
Familial Cerebral Amyloid Angiopathy
|
Cerebral Amyloid Angiopathy, Hereditary
|
|
|
| Amyloidosis |
|
Amyloid Disease
|
Amyloid
|
|
Amyloid Degeneration
|
Amyloidosis Nos
|
|
Amyloid Deposition
|
Amyloid Infiltration
|
|
Idiopathic Amyloidosis
|
Hyaloid Degeneration
|
|
Lardaceous Degeneration
|
|
|
| Akinetic Mutism |
|
|
| Aphasia |
|
|
| Wilson Disease |
|
Hepatolenticular Degeneration
|
WD
|
|
Wilson'S Disease
|
WND
|
|
Westphal-Strumpell Syndrome
|
Copper Storage Disease
|
|
Cerebral Pseudosclerosis
|
Westphal Pseudosclerosis
|
|
Hepatolenticular Degeneration Syndrome
|
Copper Retention
|
|
Hepatocerebral Degeneration
|
Kinnier-Wilson Disease
|
|
Neurohepatic Degeneration
|
Progressive Hepatolenticular Degeneration
|
|
Lenticular Degenerative Disease
|
Wilson'S Syndrome
|
|
Lenticular Syndrome
|
|
|
| Visual Cortex Disease |
|
Visual Cortex Dysfunction
|
Visual Cortex Disorder
|
|
Visual Cortical Disorder
|
Disease Of Visual Cortex
|
|
|
| Vascular Dementia |
|
Dementia, Vascular
|
Multi Infarct Dementia
|
|
Multifocal Dementia
|
Dementia Vascular
|
|
Vascular Dementia, Susceptibility To
|
Dementia, Multi-Infarct
|
|
Multi-Infarct Dementia
|
|
|
| Visual Pathway Disease |
|
Disorder Of Visual Pathways
|
|
|
| Dementia, Lewy Body |
|
Lewy Body Dementia
|
Lewy Body Disease
|
|
Diffuse Lewy Body Disease
|
Dementia With Lewy Bodies
|
|
DLB
|
Autosomal Dominant Diffuse Lewy Body Disease
|
|
Cortical Lewy Body Disease
|
Dementia, Lewy Body, Susceptibility To
|
|
Lewy Body Dementia, Susceptibility To
|
Senile Dementia Of The Lewy Body Type
|
|
Dementia Of The Lewy Body Type
|
Lbd
|
|
Diffuse Lewy Body Disease With Gaze Palsy
|
Dysphasic Dementia Hereditary
|
|
Lewy Body Type Senile Dementia
|
Lewy Body Variant Of Alzheimer Disease
|
|
Lewy Bodies
|
Lewy Body
|
|
Dlbd - [Diffuse Lewy Body Disease]
|
Clbd - [Cortical Lewy Body Disease]
|
|
|
| Dentatorubral-Pallidoluysian Atrophy |
|
DRPLA
|
Naito-Oyanagi Disease
|
|
Haw River Syndrome
|
Myoclonic Epilepsy With Choreoathetosis
|
|
Nod
|
Ataxia, Chorea, Seizures, And Dementia
|
|
Dentatorubropallidoluysian Atrophy
|
Hrs
|
|
Naito Oyanagi Disease
|
Dentatorubral Pallidoluysian Atrophy
|
|
Dentatorubro-Pallidoluysian Atrophy
|
Myoclonic Epilepsies, Progressive
|
|
Atrophy, Pallidoluysian, Dentatorubral
|
|
|
| Temporal Lobe Epilepsy |
|
Epilepsy, Temporal Lobe
|
Epilepsy Temporal Lobe
|
|
|
| Louping Ill |
|
|
| Neuroblastoma |
|
Nb
|
Neuroblastoma, Susceptibility To
|
|
Neuroblastomas
|
Central Neuroblastoma
|
|
|
| Multiple System Atrophy 1 |
|
Multiple System Atrophy
|
Shy-Drager Syndrome
|
|
Msa
|
MSA1
|
|
Multiple System Atrophy 1, Susceptibility To
|
Sporadic Olivopontocerebellar Atrophy
|
|
Multisystem Atrophy
|
Msa1, Susceptibility To
|
|
Multiple System Atrophy, Susceptibility To
|
Opca
|
|
Progressive Autonomic Failure With Multiple System Atrophy
|
Sds
|
|
|
| Frontotemporal Dementia |
|
Pallidopontonigral Degeneration
|
Frontotemporal Lobar Degeneration
|
|
Semantic Dementia
|
FTD
|
|
Frontotemporal Lobe Dementia
|
Multiple System Tauopathy With Presenile Dementia
|
|
Dementia, Frontotemporal
|
Frontotemporal Dementia With Parkinsonism
|
|
Mstd
|
Frontotemporal Lobar Degeneration With Tau Inclusions
|
|
Ftld With Tau Inclusions
|
Dementia, Frontotemporal, With Parkinsonism
|
|
Fldem
|
Ftdp17
|
|
Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex
|
Ddpac
|
|
Wilhelmsen-Lynch Disease
|
Wld
|
|
Ppnd
|
Dementia, Frontotemporal, With Or Without Parkinsonism
|
|
Semantic Primary Progressive Aphasia
|
Semantic Variant Ppa
|
|
Wilhemsen-Lynch Disease
|
Frontotemporal Dementia-Amyotrophic Lateral Sclerosis
|
|
Frontotemporal Dementia And Parkinsonism Linked To Chromosome 17
|
Ftd-Als
|
|
Ftld
|
Pick Complex
|
|
Pick Disease Of The Brain
|
Frontotemporal Dementia With Parkinsonism-17
|
|
Grn-Related Frontotemporal Dementia
|
Frontotemporal Dementia With Motor Neuron Disease
|
|
Dementia In Fronto-Temporal Lobar Degeneration
|
Ftd - [Frontotemporal Dementia]
|
|
Temple Dementia
|
Frontal Lobe Dementia
|
|
|
| Supranuclear Palsy, Progressive, 1 |
|
Progressive Supranuclear Palsy
|
Steele-Richardson-Olszewski Syndrome
|
|
Supranuclear Palsy, Progressive
|
Progressive Supranuclear Ophthalmoplegia
|
|
Psp
|
PSNP1
|
|
Familial Progressive Supranuclear Palsy
|
Richardson'S Syndrome
|
|
Psp Syndrome
|
Progressive Supranuclear Palsy 1
|
|
Supranuclear Palsy Progressive
|
Ophthalmoplegia, Supranuclear, Progressive
|
|
Steele-Richardson-Olszewksi Syndrome
|
|
|
| Autosomal Dominant Cerebellar Ataxia |
|
Spinocerebellar Ataxia
|
Adca
|
|
Pierre Marie Cerebellar Ataxia
|
Ataxia, Spinocerebellar
|
|
Sca
|
Autosomal Dominant Spinocerebellar Ataxia
|
|
Spinocerebellar Ataxias
|
|
|
| Agraphia |
|
|
| Ideomotor Apraxia |
|
Apraxia, Ideomotor
|
Classic Apraxia
|
|
Ideomotor Dyspraxia
|
Limb-Kinetic Apraxia
|
|
Transcortical Apraxia
|
|
|
| Spinocerebellar Ataxia 12 |
|
Spinocerebellar Ataxia Type 12
|
SCA12
|
|
Ataxia, Spinocerebellar, Type 12
|
|
|
| Alzheimer Disease, Familial, 1 |
|
Alzheimer Disease
|
Alzheimer'S Disease
|
|
Presenile And Senile Dementia
|
AD1
|
|
Alzheimer Disease, Susceptibility To
|
Alzheimer Disease, Late-Onset, Susceptibility To
|
|
Alzheimer Disease 1, Familial
|
AD
|
|
Familial Alzheimer Disease
|
Alzheimer Disease, Late-Onset
|
|
Alzheimers Dementia
|
Alzheimer Dementia
|
|
Alzheimer Sclerosis
|
Alzheimer Syndrome
|
|
Alzheimer-Type Dementia
|
Dat
|
|
Primary Senile Degenerative Dementia
|
Sdat
|
|
Alzheimer Disease 1
|
Autosomal Dominant Alzheimer Disease
|
|
Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy
|
Late Onset Alzheimer Disease
|
|
Alzheimers Disease
|
Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy
|
|
Late-Onset Alzheimers Disease
|
Alzheimer'S Disease Pathway Kegg
|
|
Dementia Due To Alzheimer'S Disease
|
Alzheimer Disease Type 1
|
|
Alzheimers
|
|
|
| Gerstmann Syndrome |
|
Aphasia-Angular Gyrus Syndrome
|
Developmental Gerstmann Syndrome
|
|
Gs
|
Gerstmann Badal Syndrome
|
|
Gerstmann Tetrad
|
Gerstmann'S Syndrome
|
|
Developmental Gerstmann'S Syndrome
|
|
|
| Writing Disorder |
|
|
| Gait Apraxia |
|
|
| Cortical Blindness |
|
|
| Speech And Communication Disorders |
|
Language Disorder
|
Communication Disorder
|
|
Language Disorders
|
Communication Disorders
|
|
Speech Language Disorder
|
Speech-Language Disorder
|
|
Communication Impairment
|
Speech And Language Disorder
|
|
|
| Dystonia 25 |
|
DYT25
|
Dystonia-25
|
|
Dystonia, Type 25
|
|
|
| Torsion Dystonia 2 |
|
Dystonia 2, Torsion, Autosomal Recessive
|
|
|
| Alexia |
|
Dyslexia
|
Dyslexia, Acquired
|
|
Acquired Dyslexia
|
Aphemesthaesia
|
|
|
| Cerebral Amyloid Angiopathy, Itm2b-Related, 1 |
|
Dementia, Familial British
|
Fbd
|
|
Presenile Dementia With Spastic Ataxia
|
Familial British Dementia
|
|
Abri Amyloidosis
|
Cerebral Amyloid Angiopathy, British Type
|
|
Itm2b-Related Cerebral Amyloid Angiopathy 1
|
Familial Dementia, British Type
|
|
Cerebral Amyloid Angiopathy, Itm2b-Related 1
|
CAA-ITM2B1
|
|
Cerebral Amyloid Angiopathy British Type
|
Dementia, Familial, British
|
|
|
| Mutism |
|
|
| Visual Agnosia |
|
|
| Pseudobulbar Palsy |
|
|
| Spinocerebellar Ataxia 45 |
|
SCA45
|
Spinocerebellar Ataxia Type 45
|
|
|
| Pick Disease Of Brain |
|
Pick Disease
|
Pick'S Disease
|
|
Pick Disease Of The Brain
|
Lobar Atrophy Of Brain
|
|
Dementia With Lobar Atrophy And Neuronal Cytoplasmic Inclusions
|
Behavioral Variant Of Frontotemporal Dementia
|
|
Dementia In Pick'S Disease
|
Lobar Atrophy Of The Brain
|
|
Bvftd
|
Bv-Ftd
|
|
PIDB
|
Picks Disease
|
|
|
| Akinetopsia |
|
|
| Toxic Encephalopathy |
|
Neurotoxicity
|
Neurotoxicity Syndromes
|
|
Neurotoxicity Syndrome
|
Encephalopathy, Toxic
|
|
|
| Myopathy |
|
Muscular Diseases
|
Myopathies
|
|
|
| Cortical Deafness |
|
|
| Epilepsy |
|
Epilepsy Syndrome
|
Epileptic Syndrome
|
|
Epilepsies
|
Symptomatic Epilepsies
|
|
Post Traumatic Epilepsy
|
Traumatic Epilepsy
|
|
Traumatic Epileptic
|
Epilepsy Due To Hippocampal Sclerosis
|
|
Epilepsy With Ammon'S Horn Sclerosis
|
Epilepsy Due To Cortical Dysplasia
|
|
Epilepsy Due To Neuronal Migration Disorders
|
|
|
| Amyotrophic Lateral Sclerosis 1 |
|
Amyotrophic Lateral Sclerosis
|
ALS
|
|
Lou Gehrig Disease
|
Amyotrophic Lateral Sclerosis Type 1
|
|
Charcot Disease
|
ALS1
|
|
Amyotrophic Lateral Sclerosis, Susceptibility To
|
Fals
|
|
Lou Gehrig'S Disease
|
Mnd
|
|
Motor Neuron Disease
|
Familial Amyotrophic Lateral Sclerosis
|
|
Amyotrophic Lateral Sclerosis 1, Familial
|
Amyotrophic Lateral Sclerosis 1, Autosomal Dominant
|
|
Motor Neuron Disease, Bulbar
|
Motor Neurone Disease
|
|
Amyotrophic Lateral Sclerosis With Dementia
|
Dementia With Amyotrophic Lateral Sclerosis
|
|
Motor Neuron Disease, Amyotrophic Lateral Sclerosis
|
Sclerosis, Lateral, Amyotrophic
|
|
Sclerosis, Lateral, Amyotrophic, Type 1
|
Amyotrophic Sclerosis
|
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Als - [Amyotrophic Lateral Sclerosis]
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Wasting Palsy
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Amyotrophic Paralysis
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Amyotrophy Lateral Sclerosis
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Wasting Paralysis
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Spinal Progressive Amyotrophy
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Progressive Atrophic Paralysis
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| Warburg Micro Syndrome 3 |
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| Warburg Micro Syndrome 2 |
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| Choreatic Disease |
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| Neuromuscular Disease |
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Neuromuscular Diseases
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Neuromuscular Disorders
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Neuromuscular Disorder
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| Cerebellar Disease |
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Cerebellar Diseases
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Cerebellar Dysfunction
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Cerebellar Abnormality
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Cerebellar Disorders
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| Movement Disease |
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Movement Disorders
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Movement Disorder
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| Nervous System Disease |
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Abnormality Of The Nervous System
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Nervous System Diseases
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Nervous System Disorder
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| Parkinson Disease, Late-Onset |
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Parkinson Disease
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Parkinson'S Disease
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PD
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PARK
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Parkinson Disease, Susceptibility To
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Late Onset Parkinson'S Disease
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Late Onset Parkinson Disease
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Paralysis Agitans
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Primary Parkinsonism
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Idiopathic Parkinson Disease
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Parkinson'S
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Parkinson Disease, Late-Onset, Susceptibility To
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Parkinson Disease, Age Of Onset, Modifier
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Lewy Body Parkinson Disease
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Idiopathic Parkinson'S Disease
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Pd - [Parkinson Disease]
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Parkinson Disease Nos
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Parkinson, Nos
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Primary Parkinson Disease
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