| 疾病名称 |
别名 |
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| Myopathy, Isolated Mitochondrial, Autosomal Dominant |
|
Autosomal Dominant Mitochondrial Myopathy With Exercise Intolerance
|
IMMD
|
|
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| Spinal Muscular Atrophy, Jokela Type |
|
SMAJ
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Lower Motor Neuron Syndrome With Late-Adult Onset
|
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Losmon
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Late-Onset Spinal Motor Neuronopathy
|
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Atrophy, Muscular, Spinal, Jokela Type
|
|
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| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 2 |
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FTDALS2
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Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-2
|
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Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis, Type 2
|
|
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| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1 |
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FTDALS1
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Frontotemporal Dementia And/Or Motor Neuron Disease
|
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Ftdmnd
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Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia
|
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Alsftd
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Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis
|
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Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-1
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Frontotemporal Dementia With Motor Neuron Disease
|
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Ftdals
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Ftd-Als
|
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Ftd-Mnd
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Frontotemporal Dementia With Amyotrophic Lateral Sclerosis
|
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Amyotrophic Lateral Sclerosis With Frontotemporal Dementia 1
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Amyotrophic Lateral Sclerosis/Frontotemporal Dementia
|
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Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis
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Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia 1
|
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Frontotemporal Lobar Degeneration
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Grn-Related Frontotemporal Dementia
|
|
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| Amyotrophic Lateral Sclerosis 1 |
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Amyotrophic Lateral Sclerosis
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ALS
|
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Lou Gehrig Disease
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Amyotrophic Lateral Sclerosis Type 1
|
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Charcot Disease
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ALS1
|
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Amyotrophic Lateral Sclerosis, Susceptibility To
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Fals
|
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Lou Gehrig'S Disease
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Mnd
|
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Motor Neuron Disease
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Familial Amyotrophic Lateral Sclerosis
|
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Amyotrophic Lateral Sclerosis 1, Familial
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Amyotrophic Lateral Sclerosis 1, Autosomal Dominant
|
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Motor Neuron Disease, Bulbar
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Motor Neurone Disease
|
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Amyotrophic Lateral Sclerosis With Dementia
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Dementia With Amyotrophic Lateral Sclerosis
|
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Motor Neuron Disease, Amyotrophic Lateral Sclerosis
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Sclerosis, Lateral, Amyotrophic
|
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Sclerosis, Lateral, Amyotrophic, Type 1
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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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| Lateral Sclerosis |
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Primary Lateral Sclerosis
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Adult-Onset Primary Lateral Sclerosis
|
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Adult-Onset Pls
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Motor Neuron Disease
|
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Pls
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Pls - [Primary Lateral Sclerosis]
|
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Lateral Spinal Sclerosis
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Lateral Complete Paralysis
|
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Lateral Incomplete Paralysis
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Lateral Paralysis
|
|
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| Frontotemporal Dementia |
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Pallidopontonigral Degeneration
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Frontotemporal Lobar Degeneration
|
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Semantic Dementia
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FTD
|
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Frontotemporal Lobe Dementia
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Multiple System Tauopathy With Presenile Dementia
|
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Dementia, Frontotemporal
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Frontotemporal Dementia With Parkinsonism
|
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Mstd
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Frontotemporal Lobar Degeneration With Tau Inclusions
|
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Ftld With Tau Inclusions
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Dementia, Frontotemporal, With Parkinsonism
|
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Fldem
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Ftdp17
|
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Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex
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Ddpac
|
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Wilhelmsen-Lynch Disease
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Wld
|
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Ppnd
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Dementia, Frontotemporal, With Or Without Parkinsonism
|
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Semantic Primary Progressive Aphasia
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Semantic Variant Ppa
|
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Wilhemsen-Lynch Disease
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Frontotemporal Dementia-Amyotrophic Lateral Sclerosis
|
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Frontotemporal Dementia And Parkinsonism Linked To Chromosome 17
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Ftd-Als
|
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Ftld
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Pick Complex
|
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Pick Disease Of The Brain
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Frontotemporal Dementia With Parkinsonism-17
|
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Grn-Related Frontotemporal Dementia
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Frontotemporal Dementia With Motor Neuron Disease
|
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Dementia In Fronto-Temporal Lobar Degeneration
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Ftd - [Frontotemporal Dementia]
|
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Temple Dementia
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Frontal Lobe Dementia
|
|
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| Dementia |
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Dementias
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Presenile Dementia
|
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Alzheimer Type Dementia
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Alzheimer Sclerosis
|
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Alzheimer Disease Dementia
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Alzheimer Dementia
|
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Primary Degenerative Alzheimer Type Dementia
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End Stage Alzheimer'S Dementia
|
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Alzheimer'S Type Atypical Dementia
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Alzheimer Type Presenile Dementia
|
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Early Onset Alzheimer Dementia
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Dementia In Alzheimer Disease Type 2
|
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Dementia In Alzheimer Disease With Early Onset
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Early Onset Alzheimer Type Dementia, Uncomplicated
|
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Primary Degenerative Alzheimer Type Dementia, Early Onset
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Primary Degenerative Alzheimer Type Dementia, Presenile Onset, Uncomplicated
|
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Alzheimer Disease Dementia With Early Onset
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Presenile Sclerosis
|
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Presenile Brain Sclerosis
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Presenile Alzheimer Brain Sclerosis
|
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Late Onset Alzheimer Dementia
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Dementia In Alzheimer Disease Type 1
|
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Dementia In Alzheimer Disease With Late Onset
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Primary Degenerative Alzheimer Type Dementia, Late Onset
|
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Sdat - [Senile Dementia, Alzheimer Type]
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Alzheimer Disease Dementia With Late Onset
|
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Late Onset Alzheimer Brain Sclerosis
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Senile Alzheimer Brain Disease
|
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Senile Alzheimer Brain Sclerosis
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Senile Primary Degenerative Alzheimer Type Dementia
|
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Senile Dementia Of The Alzheimer Type
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Arteriosclerotic Dementia
|
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Strategic-Infarct Dementia
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Post Stroke Dementia
|
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Vascular Cognitive Impairment
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Vascular Dementia
|
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Dementia Of The Lewy Body Type
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Dementia With Lewy Bodies
|
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Sdlt - [Senile Dementia Of The Lewy Body Type]
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Senile Dementia Of The Lewy Body Type
|
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Alcohol-Related Dementia
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Alcoholic Dementia Nos
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Alcohol-Induced Dementia
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Alcoholic Brain Syndrome
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Chronic Alcoholic Brain Syndrome
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Alcohol Dementia
|
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Late Onset Alcoholic Psychosis
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Residual And Late-Onset Alcohol-Induced Psychotic Disorder
|
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Mental And Behavioural Disorders Due To Use Of Sedatives Or Hypnotics, Residual And Late-Onset Psychotic Disorder
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Late-Onset Psychoactive Substance-Induced Psychotic Disorder
|
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Inhalant Dementia
|
Volatile Solvents Dementia
|
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Dementia In Paralysis Agitans
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Pdd - [Parkinson Disease Dementia]
|
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Dementia Syndrome Of Parkinson Disease
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Dementia In Parkinson Disease
|
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Parkinson Related Dementia
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Dementia In Huntington Chorea
|
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Hiv - [Human Immunodeficiency Virus] Dementia
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Hiv- [Human Immunodeficiency Virus] Associated Cognitive Motor Complex
|
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Hiv- [Human Immunodeficiency Virus] Associated Dementia Complex
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Aids - [Acquired Immunodeficiency Syndrome] Dementia Complex
|
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Aids Related Dementia
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Dementia Due To Niacin Deficiency
|
|
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| Motor Neuron Disease |
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Anterior Horn Cell Disease
|
Motor Neuron Diseases
|
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Mnd - [Motor Neurone Disease]
|
Lou Gehrig Disease
|
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Creeping Palsy
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Creeping Paralysis
|
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Bulbar Motor Neuron Disease
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Bulbar Syndrome
|
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Anterior Horn Cell Disorder
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Hereditary Motor Neuron Disease
|
|
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| Mitochondrial Myopathy |
|
Mitochondrial Myopathies
|
Mitochondrial Cytopathy
|
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Myopathies In Mitochondrial Disorders
|
|
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| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 3 |
|
FTDALS3
|
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-3
|
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Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis, Type 3
|
|
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| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 4 |
|
FTDALS4
|
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-4
|
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Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis, Type 4
|
|
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| Myopathy |
|
Muscular Diseases
|
Myopathies
|
|
|
| Spinocerebellar Ataxia 2 |
|
Spinocerebellar Ataxia Type 2
|
SCA2
|
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Amyotrophic Lateral Sclerosis 13
|
Spinocerebellar Degeneration With Slow Eye Movements
|
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SDSEM
|
Spinocerebellar Atrophy Ii
|
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Olivopontocerebellar Atrophy Ii
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Opca2
|
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Cerebellar Degeneration With Slow Eye Movements
|
Wadia-Swami Syndrome
|
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Amyotrophic Lateral Sclerosis Type 13
|
ALS13
|
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Olivopontocerebellar Atrophy Holguin Type
|
Spinocerebellar Ataxia Cuban Type
|
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Olivopontocerebellar Atrophy, Holguin Type
|
Spinocerebellar Ataxia, Cuban Type
|
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Amyotrophic Lateral Sclerosis, Susceptibility To, 13
|
Olivopontocerebellar Atrophy 2
|
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Sca 2
|
Spinocerebellar Ataxia With Slow Eye Movements
|
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Spinocerebellar Atrophy 2
|
Wadia Swami Syndrome
|
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Opca Ii
|
Spinocerebellar Ataxia-2
|
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Ataxia, Spinocerebellar, Type 2
|
|
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| Amyotrophic Lateral Sclerosis 18 |
|
Amyotrophic Lateral Sclerosis Type 18
|
ALS18
|
|
Sclerosis, Lateral, Amyotrophic, Type 18
|
|
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| Spinal Muscular Atrophy |
|
Sma
|
5q Sma
|
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Proximal Sma
|
Sma-Associated Sma
|
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Spinal Amyotrophies
|
Spinal Amyotrophy
|
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Spinal Muscle Degeneration
|
Spinal Muscle Wasting
|
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Muscular Atrophy Spinal
|
Atrophy, Muscular, Spinal
|
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Hereditary Motor Neuronopathy
|
Progressive Muscular Atrophy
|
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Sma - [Spinal Muscular Atrophy]
|
|
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| Muscular Atrophy |
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Muscle Wasting
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Amyotrophia
|
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Wasting - Muscle
|
Skeletal Muscle Atrophy
|
|
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| Spondylometaphyseal Dysplasia, Axial |
|
Axial Spondylometaphyseal Dysplasia
|
SMDAX
|
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Axial Smd
|
Smd Axial
|
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Smd, Axial
|
Spondylometaphyseal Dysplasia Axial Type
|
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Dysplasia, Spondylometaphyseal, Axial
|
|
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| Amyotrophic Lateral Sclerosis Type 22 |
|
Als 22
|
Amyotrohpic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia
|
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Amyotrophic Lateral Sclerosis 22
|
|
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| Combined Oxidative Phosphorylation Deficiency 37 |
|
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| Progressive Muscular Atrophy |
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Progressive Spinal Muscular Atrophy
|
Pure Progressive Muscular Atrophy
|
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Pma
|
Hereditary Spinal Muscle Atrophy
|
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Pma - [Progressive Muscular Atrophy]
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Progressive Muscle Atrophy
|
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Progressive Spinal Muscle Atrophy
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Duchenne-Aran Atrophy
|
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Duchenne-Aran Muscle Atrophy
|
Hereditary Sma - [Spinal Muscle Atrophy]
|
|
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| Amyotrophic Lateral Sclerosis Type 14 |
|
Als14
|
Amyotrophic Lateral Sclerosis 14
|
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Amyotrophic Lateral Sclerosis, With Or Without Frontotemporal Dementia
|
Amyotrophic Lateral Sclerosis 14 With Or Without Frontotemporal Dementia
|
|
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| Charcot-Marie-Tooth Disease, Axonal, Type 2e |
|
Charcot-Marie-Tooth Disease Type 2
|
CMT2E
|
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CMT2S
|
CMT2Y
|
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Charcot-Marie-Tooth Disease Type 2e
|
Charcot-Marie-Tooth Disease Type 2y
|
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Charcot-Marie-Tooth Disease Axonal Type 2s
|
Charcot-Marie-Tooth Disease, Axonal, Type 2s
|
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Charcot-Marie-Tooth Disease, Type 2e
|
Hereditary Motor And Sensory Neuropathy Type 2
|
|
Charcot-Marie-Tooth Neuropathy, Type 2s
|
Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, Type 2s
|
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Charcot-Marie-Tooth Disease, Axonal, Type 2y
|
Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2y
|
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Charcot-Marie-Tooth Neuropathy, Type 2y
|
Charcot-Marie-Tooth Disease, Type 2y
|
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Autosomal Dominant Charcot-Marie-Tooth Disease Type 2e
|
Charcot-Marie-Tooth Neuropathy Type 2e
|
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Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Vcp Mutation
|
Cmt2 Due To Vcp Mutation
|
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Charcot-Marie-Tooth Disease Type 2s
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2
|
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Autosomal Dominant Axonal Charcot-Marie-Tooth Disease
|
Cmt2
|
|
Charcot-Marie-Tooth Neuropathy, Type 2e
|
Hereditary Motor And Sensory Neuropathy Guadalajara Neuronal Type
|
|
Hereditary Motor And Sensory Neuropathy Okinawa Type
|
Autosomal Dominant Axonal Charcot-Marie-Tooth Type 2y
|
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Charcot-Marie-Tooth Neuropathy Type 2y
|
Autosomal Recessive Axonal Charcot-Marie-Tooth Type 2s
|
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Charcot-Marie-Tooth Neuropathy Type 2s
|
Charcot-Marie-Tooth Type 2
|
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Autosomal Dominant Charcot-Marie-Tooth Disease Type 2y
|
Charcot-Marie-Tooth Disease 2e
|
|
Charcot-Marie-Tooth Disease Axonal Type 2e
|
Charcot-Marie-Tooth Disease Neuronal Type 2e
|
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Charcot-Marie-Tooth Disease 2s
|
Charcot-Marie-Tooth Neuropathy Axonal Type 2s
|
|
Charcot-Marie-Tooth Disease 2y
|
Charcot-Marie-Tooth Disease, Type 2
|
|
Hereditary Motor And Sensory-Neuropathy Type Ii
|
|
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| Moyamoya Disease 1 |
|
Moyamoya Disease
|
Spontaneous Occlusion Of The Circle Of Willis
|
|
Mymy
|
Progressive Intracranial Arterial Occlusion
|
|
Moyamoya Syndrome
|
MYMY1
|
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Cerebrovascular Moyamoya Disease
|
Moya-Moya Disease
|
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Progressive Intracranial Occlusive Arteropathy
|
Idiopathic Moyamoya Disease
|
|
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| Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia |
|
Ibmpfd
|
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia
|
|
Pagetoid Amyotrophic Lateral Sclerosis
|
Pagetoid Neuroskeletal Syndrome
|
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Inclusion Body Myopathy With Paget Disease Of Bone And/Or Frontotemporal Dementia
|
Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone And/Or Frontotemporal Dementia
|
|
Multisystem Proteinopathy
|
Limb-Girdle Muscular Dystrophy With Paget Disease Of Bone
|
|
Inclusion Body Myopathy With Paget'S Disease Of Bone And Frontotemporal Dementia
|
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dement
|
|
Lower Motor Neuron Degeneration With Paget-Like Bone Disease
|
Muscular Dystrophy, Limb-Girdle, With Paget Disease Of Bone
|
|
Myopathy, Inclusion Body, With Early-Onset Paget Disease And Frontotemporal Dementia
|
|
|
| Charcot-Marie-Tooth Disease |
|
Cmt
|
Hmsn
|
|
Hereditary Motor And Sensory Neuropathy
|
Pma
|
|
Cmt - Charcot-Marie-Tooth Disease
|
Charcot Marie Tooth Disease
|
|
Charcot-Marie-Tooth Hereditary Neuropathy
|
Charcot-Marie-Tooth Syndrome
|
|
Peroneal Muscular Atrophy
|
Hereditary Motor And Sensory Neuropathies
|
|
|
| Neuromuscular Disease |
|
Neuromuscular Diseases
|
Neuromuscular Disorders
|
|
Neuromuscular Disorder
|
|
|
| Hereditary Spastic Paraplegia |
|
Familial Spastic Paraplegia
|
Hereditary Spastic Paraparesis
|
|
Strumpell-Lorrain Disease
|
Familial Spastic Paraparesis
|
|
Hsp
|
Spg
|
|
Strümpell-Lorrain Disease
|
Spastic Paraplegia, Hereditary
|
|
French Settlement Disease
|
Strumpell-Lorrain Syndrome
|
|
Fsp
|
Spastic Paraplegia, Familial
|
|
Spastic Paraplegia Hereditary
|
Spastic Paraplegia 3, Autosomal Dominant
|
|
Spastic Paraparesis
|
Hereditary Spastic Paralysis
|
|
Familial Spastic Paralysis
|
Hereditary Spastic Ataxia
|
|
|
