| 疾病名称 |
别名 |
|
| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1 |
|
FTDALS1
|
Frontotemporal Dementia And/Or Motor Neuron Disease
|
|
Ftdmnd
|
Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia
|
|
Alsftd
|
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis
|
|
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-1
|
Frontotemporal Dementia With Motor Neuron Disease
|
|
Ftdals
|
Ftd-Als
|
|
Ftd-Mnd
|
Frontotemporal Dementia With Amyotrophic Lateral Sclerosis
|
|
Amyotrophic Lateral Sclerosis With Frontotemporal Dementia 1
|
Amyotrophic Lateral Sclerosis/Frontotemporal Dementia
|
|
Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis
|
Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia 1
|
|
Frontotemporal Lobar Degeneration
|
Grn-Related Frontotemporal Dementia
|
|
|
| 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
|
|
Als - [Amyotrophic Lateral Sclerosis]
|
Wasting Palsy
|
|
Amyotrophic Paralysis
|
Amyotrophy Lateral Sclerosis
|
|
Wasting Paralysis
|
Spinal Progressive Amyotrophy
|
|
Progressive Atrophic Paralysis
|
|
|
| Huntington Disease-Like Syndrome Due To C9orf72 Expansions |
|
C9orf72-Related Huntington Disease Phenocopy
|
C9orf72-Related Huntington Disease-Like Syndrome
|
|
Huntington Disease Phenocopy Due To C9orf72 Expansions
|
|
|
| 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
|
|
|
| Progressive Non-Fluent Aphasia |
|
Non-Fluent Variant Ppa
|
Progressive Nonfluent Aphasia
|
|
Non-Fluent Primary Progressive Aphasia
|
Agramatic Variant Of Ppa
|
|
Agramatic Variant Of Primary Progressive Aphasia
|
Primary Progressive Non Fluent Aphasia
|
|
Primary Progressive Nonfluent Aphasia
|
|
|
| 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
|
|
|
| Lateral Sclerosis |
|
Primary Lateral Sclerosis
|
Adult-Onset Primary Lateral Sclerosis
|
|
Adult-Onset Pls
|
Motor Neuron Disease
|
|
Pls
|
Pls - [Primary Lateral Sclerosis]
|
|
Lateral Spinal Sclerosis
|
Lateral Complete Paralysis
|
|
Lateral Incomplete Paralysis
|
Lateral Paralysis
|
|
|
| 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
|
|
|
| Aphasia |
|
|
| Speech And Communication Disorders |
|
Language Disorder
|
Communication Disorder
|
|
Language Disorders
|
Communication Disorders
|
|
Speech Language Disorder
|
Speech-Language Disorder
|
|
Communication Impairment
|
Speech And Language Disorder
|
|
|
| Spinocerebellar Ataxia 2 |
|
Spinocerebellar Ataxia Type 2
|
SCA2
|
|
Amyotrophic Lateral Sclerosis 13
|
Spinocerebellar Degeneration With Slow Eye Movements
|
|
SDSEM
|
Spinocerebellar Atrophy Ii
|
|
Olivopontocerebellar Atrophy Ii
|
Opca2
|
|
Cerebellar Degeneration With Slow Eye Movements
|
Wadia-Swami Syndrome
|
|
Amyotrophic Lateral Sclerosis Type 13
|
ALS13
|
|
Olivopontocerebellar Atrophy Holguin Type
|
Spinocerebellar Ataxia Cuban Type
|
|
Olivopontocerebellar Atrophy, Holguin Type
|
Spinocerebellar Ataxia, Cuban Type
|
|
Amyotrophic Lateral Sclerosis, Susceptibility To, 13
|
Olivopontocerebellar Atrophy 2
|
|
Sca 2
|
Spinocerebellar Ataxia With Slow Eye Movements
|
|
Spinocerebellar Atrophy 2
|
Wadia Swami Syndrome
|
|
Opca Ii
|
Spinocerebellar Ataxia-2
|
|
Ataxia, Spinocerebellar, Type 2
|
|
|
| Associative Agnosia |
|
|
| Spinocerebellar Ataxia 36 |
|
Spinocerebellar Ataxia Type 36
|
SCA36
|
|
Asidan Ataxia
|
Costa De Morte Ataxia
|
|
Asidan
|
Ataxia, Spinocerebellar, Type 36
|
|
|
| Cardiomyopathy, Familial Hypertrophic, 20 |
|
Hypertrophic Cardiomyopathy 20
|
CMH20
|
|
Cardiomyopathy, Hypertrophic, 20
|
Cardiomyopathy Familial Hypertrophic 20
|
|
Cardiomyopathy, Familial Hypertrophic 20
|
Cardiomyopathy, Hypertrophic, Familial, Type 20
|
|
|
| Nominal Aphasia |
|
|
| Motor Neuron Disease |
|
Anterior Horn Cell Disease
|
Motor Neuron Diseases
|
|
Mnd - [Motor Neurone Disease]
|
Lou Gehrig Disease
|
|
Creeping Palsy
|
Creeping Paralysis
|
|
Bulbar Motor Neuron Disease
|
Bulbar Syndrome
|
|
Anterior Horn Cell Disorder
|
Hereditary Motor Neuron Disease
|
|
|
| Dysgraphia |
|
|
| Progressive Bulbar Palsy |
|
Bulbar Palsy, Progressive
|
Progressive Bulbar Atrophy
|
|
Bulbar Palsy
|
Pbp - [Progressive Bulbar Palsy]
|
|
Progressive Bulbar Paralysis
|
Bulbar Paralysis
|
|
Chronic Bulbar Palsy
|
Chronic Bulbar Paralysis
|
|
Supranuclear Bulbar Paralysis
|
|
|
| X-Linked Hereditary Ataxia |
|
|
| Writing Disorder |
|
|
| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 2 |
|
FTDALS2
|
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-2
|
|
Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis, Type 2
|
|
|
| Phonagnosia |
|
|
| Anosognosia |
|
|
| Progressive Muscular Atrophy |
|
Progressive Spinal Muscular Atrophy
|
Pure Progressive Muscular Atrophy
|
|
Pma
|
Hereditary Spinal Muscle Atrophy
|
|
Pma - [Progressive Muscular Atrophy]
|
Progressive Muscle Atrophy
|
|
Progressive Spinal Muscle Atrophy
|
Duchenne-Aran Atrophy
|
|
Duchenne-Aran Muscle Atrophy
|
Hereditary Sma - [Spinal Muscle Atrophy]
|
|
|
| Amyotrophic Lateral Sclerosis 18 |
|
Amyotrophic Lateral Sclerosis Type 18
|
ALS18
|
|
Sclerosis, Lateral, Amyotrophic, Type 18
|
|
|
| Fragile X-Associated Tremor/Ataxia Syndrome |
|
Fxtas Syndrome
|
Fragile X Tremor/Ataxia Syndrome
|
|
Fxtas
|
|
|
| Muscular Atrophy |
|
Muscle Wasting
|
Amyotrophia
|
|
Wasting - Muscle
|
Skeletal Muscle Atrophy
|
|
|
| Prosopagnosia |
|
|
| Amyotrophic Lateral Sclerosis 19 |
|
Amyotrophic Lateral Sclerosis Type 19
|
ALS19
|
|
Sclerosis, Lateral, Amyotrophic, Type 19
|
|
|
| Spinocerebellar Ataxia 8 |
|
Spinocerebellar Ataxia Type 8
|
SCA8
|
|
Ataxia, Spinocerebellar, Type 8
|
|
|
| Essential Tremor |
|
Benign Essential Tremor
|
Familial Tremor
|
|
Hereditary Essential Tremor
|
Essential Hereditary Tremor
|
|
Shaky Hand Syndrome
|
Benign Essential Tremor Syndrome
|
|
Tremor Hereditary Essential
|
Essential Tremor, Susceptibility To
|
|
Tremor, Hereditary Essential
|
|
|
| Multisystem Proteinopathy |
|
|
| Amyotrophic Lateral Sclerosis Type 14 |
|
Als14
|
Amyotrophic Lateral Sclerosis 14
|
|
Amyotrophic Lateral Sclerosis, With Or Without Frontotemporal Dementia
|
Amyotrophic Lateral Sclerosis 14 With Or Without Frontotemporal Dementia
|
|
|
| Amyotrophic Lateral Sclerosis Type 15 |
|
Amyotrophic Lateral Sclerosis 15, With Or Without Frontotemporal Dementia
|
Als15
|
|
Amyotrophic Lateral Sclerosis 15
|
|
|
| Agraphia |
|
|
| Amyotrophic Lateral Sclerosis Type 22 |
|
Als 22
|
Amyotrohpic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia
|
|
Amyotrophic Lateral Sclerosis 22
|
|
|
| Spinocerebellar Ataxia 31 |
|
Spinocerebellar Ataxia Type 31
|
SCA31
|
|
Spinocerebellar Ataxia 16q22-Linked
|
Spinocerebellar Ataxia, 16q22-Linked
|
|
Pure Spinocerebellar Ataxia Japanese Type
|
Sca4 Pure Japanese Type
|
|
Ataxia, Spinocerebellar, Type 31
|
|
|
| Postpoliomyelitis Syndrome |
|
Postpolio Syndrome
|
Post-Polio Syndrome
|
|
Post Polio Syndrome
|
Polio Late Effects
|
|
Post-Polio Muscular Atrophy
|
Post-Polio Sequelae
|
|
Post-Poliomyelitic Syndrome
|
Postpolio Sequelae
|
|
Postpoliomyelitic Syndrome
|
Postpoliomyelitis Sequelae
|
|
|
| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 3 |
|
FTDALS3
|
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-3
|
|
Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis, Type 3
|
|
|
| Myotonic Dystrophy 2 |
|
Myotonic Dystrophy Type 2
|
Proximal Myotonic Myopathy
|
|
Promm
|
Ricker Syndrome
|
|
DM2
|
Dystrophia Myotonica 2
|
|
Myotonic Myopathy, Proximal
|
Myotonic Disorders
|
|
Dystrophia Myotonica Type 2
|
Proximal Myotonic Dystrophy
|
|
Ricker Disease
|
Myotonic Dystrophy, Type 2
|
|
Dystrophy, Myotonic, Type 2
|
|
|
| Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 |
|
Guam Disease
|
Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex Of Guam
|
|
Als-Pdc
|
Lytico-Bodig Disease
|
|
Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Complex
|
Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1, Susceptibility To
|
|
Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex, Susceptibility To
|
Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex
|
|
Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Of Guam Syndrome
|
Parkinsonism-Dementia-Als Complex
|
|
Pdals
|
Amyotrophic Lateral Sclerosis, Parkinsonism/Dementia Complex Of Guam
|
|
Parkinson-Dementia Complex Of Guam
|
G-Pdc
|
|
Guam Parkinsonism-Dementia Complex
|
ALS-PDC1
|
|
Als/Pdc Of Guam
|
Amyotrophic Lateral Sclerosis
|
|
Sclerosis, Lateral, Amyotrophic/Parkinsonism/Dementia Complex 1
|
Amyotrophic Lateral Sclerosis, Guam Form
|
|
Parkinsonian Disorders
|
|
|
| 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
|
|
|
| Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia |
|
Amyotrophic Lateral Sclerosis Type 10
|
ALS10
|
|
Amyotrophic Lateral Sclerosis 10, With Or Without Ftd
|
Frontotemporal Lobar Degeneration, Tardbp-Related
|
|
Amyotrophic Lateral Sclerosis 10
|
Amyotrophic Lateral Sclerosis 10, With Or Without Frontotemporal Dementia
|
|
Tardbp-Related Frontotemporal Lobar Degeneration With Tdp43 Inclusions
|
Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia And With Tdp43 Inclusions
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 10
|
|
|
| Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone With Or Without Frontotemporal Dementia 2 |
|
Ibmpfd2
|
Msp2
|
|
Multisystem Proteinopathy 2
|
|
|
| Myotonic Disease |
|
Myotonic Disorders
|
Myotonic Syndrome
|
|
Symptomatic Myotonia
|
|
|
| Ideomotor Apraxia |
|
Apraxia, Ideomotor
|
Classic Apraxia
|
|
Ideomotor Dyspraxia
|
Limb-Kinetic Apraxia
|
|
Transcortical Apraxia
|
|
|
| Perry Syndrome |
|
Parkinsonism With Alveolar Hypoventilation And Mental Depression
|
PERRYS
|
|
|
| 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
|
|
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
|
|
|
| Pseudobulbar Palsy |
|
|
| Spinal And Bulbar Muscular Atrophy, X-Linked 1 |
|
Kennedy Disease
|
Sbma
|
|
Spinal And Bulbar Muscular Atrophy
|
Kennedy'S Disease
|
|
X-Linked Spinal And Bulbar Muscular Atrophy
|
SMAX1
|
|
Kd
|
Kennedy Spinal And Bulbar Muscular Atrophy
|
|
Spinobulbar Muscular Atrophy
|
Bulbospinal Muscular Atrophy, X-Linked
|
|
Bulbospinal Neuronopathy, X-Linked Recessive
|
Xbsn
|
|
Spinal And Bulbar Muscular Atrophy Of Kennedy
|
Bulbospinal Muscular Atrophy
|
|
X-Linked Bulbospinal Amyotrophy
|
Bulbo-Spinal Atrophy, X-Linked
|
|
Spinal Bulbar Muscular Atrophy
|
X-Linked Bulbo-Spinal Atrophy
|
|
X-Linked Spinal Bulbar Muscular Atrophy
|
X-Linked Bsma
|
|
X-Linked Bulbospinal Muscular Atrophy
|
Spinal And Bulbar Muscular Atrophy X-Linked 1
|
|
Bulbospinal Muscular Atrophy X-Linked
|
Bulbospinal Neuronopathy X-Linked Recessive
|
|
Kennedy Disease)
|
Kennedy Syndrome
|
|
Atrophy, Muscular, Spinal And Bulbar, Kennedy Type
|
Atrophy, Muscular, Spinobulbar
|
|
Bulbospinal Neuronopathy
|
|
|
| Amyotrophic Lateral Sclerosis 20 |
|
Amyotrophic Lateral Sclerosis Type 20
|
ALS20
|
|
Sclerosis, Lateral, Amyotrophic, Type 20
|
|
|
| Obsessive-Compulsive Disorder |
|
OCD
|
Obsessive-Compulsive Disorder, Susceptibility To
|
|
Anancastic Neurosis
|
Obsessive Compulsive Disorder
|
|
Anankastic Neurosis
|
Obsessive-Compulsive Neurosis
|
|
Obsessive Compulsive Behavior
|
|
|
| Amyotrophic Lateral Sclerosis 16, Juvenile |
|
Amyotrophic Lateral Sclerosis Type 16
|
ALS16
|
|
Amyotrophic Lateral Sclerosis 16
|
Sclerosis, Lateral, Amyotrophic, Type 16, Juvenile
|
|
|
| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 4 |
|
FTDALS4
|
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-4
|
|
Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis, Type 4
|
|
|
| Restless Legs Syndrome |
|
Wed
|
Willis-Ekbom Disease
|
|
Restless Leg Syndrome
|
Ekbom Syndrome
|
|
Wittmaack-Ekbom Syndrome
|
Willis Ekbom Disease
|
|
Ekbom'S Syndrome
|
Rls
|
|
Restless Legs
|
Restless Legs Syndrome, Susceptibility To
|
|
|
| Alexia |
|
Dyslexia
|
Dyslexia, Acquired
|
|
Acquired Dyslexia
|
Aphemesthaesia
|
|
|
| Pupil Disease |
|
Pupil Disorders
|
Pupillary Disorder
|
|
|
| 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
|
|
|
| Amyotrophic Lateral Sclerosis 8 |
|
Amyotrophic Lateral Sclerosis Type 8
|
ALS8
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 8
|
|
|
| Amyotrophic Lateral Sclerosis 4, Juvenile |
|
Amyotrophic Lateral Sclerosis Type 4
|
ALS4
|
|
Amyotrophic Lateral Sclerosis 4
|
Dhmn With Upper Motor Neuron Signs
|
|
Distal Hereditary Motor Neuropathy With Upper Motor Neuron Signs
|
Neuronopathy, Distal Hereditary Motor, With Pyramidal Features
|
|
Als 4
|
Distal Hereditary Motor Neuropathy With Pyramidal Features
|
|
Amyotrophic Lateral Sclerosis Juvenile 4
|
Neuronopathy Distal Hereditary Motor With Pyramidal Features
|
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Sclerosis, Lateral, Amyotrophic, Type Type 4
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| Huntington Disease-Like 2 |
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HDL2
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Huntington'S Disease-Like 2
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Huntington Disease-Like, Type 2
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| Echolalia |
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| Creutzfeldt-Jakob Disease |
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Variant Creutzfeldt-Jakob Disease
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CJD
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Bovine Spongiform Encephalopathy
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Vcjd
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Inherited Creutzfeldt-Jakob Disease
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Creutzfeldt-Jakob Disease, Familial
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Creutzfeldt Jakob Disease
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Creutzfeldt-Jacob Disease
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Creutzfeldt Jacob Disease
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Sporadic Creutzfeldt-Jakob Disease
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Encephalopathy, Bovine Spongiform
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Creutzfeldt-Jakob Disease, Variant, Resistance To
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Creutzfeldt-Jakob Disease, Variant
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Creutzfeldt Jacob Syndrome
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Jakob-Creutzfeldt Disease
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Subacute Spongiform Encephalopathy
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Transmissible Virus Dementia
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New Variant Of Cjd
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Nv-Cjd
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Variant Cjd
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Variant Creutzfeldt-Jacob Disease
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Sporadic Cjd
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Inherited Cjd
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Acquired Creutzfeldt-Jakob Disease
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Variant Mcj
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Encephalopathy Bovine Spongiform
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Familial Creutzfeldt-Jakob Disease
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Creutzfeldt-Jakob Syndrome
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New Variant Creutzfeldt-Jakob Disease
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Creutzfeldt-Jakob Disease, Sporadic
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Acquired Cjd
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Scjd - [Sporadic Creutzfeldt-Jakob Disease]
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Idiopathic Creutzfeldt-Jakob Disease
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Creutzfeld-Jakob Disease Nos
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Vcjd - [Variant Creutzfeldt-Jakob Disease]
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| Amyotrophic Lateral Sclerosis Type 6 |
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Amyotrophic Lateral Sclerosis 6, Autosomal Recessive
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Als6
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Amyotrophic Lateral Sclerosis 6, With Or Without Frontotemporal Dementia
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Autosomal Recessive Amyotrophic Lateral Sclerosis 6
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Sclerosis, Lateral, Amyotrophic, Type Type 6
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Amyotrophic Lateral Sclerosis 6
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| Visual Agnosia |
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| Amyotrophic Lateral Sclerosis 11 |
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Amyotrophic Lateral Sclerosis Type 11
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ALS11
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Sclerosis, Lateral, Amyotrophic, Type Type 11
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| Dementia, Lewy Body |
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Lewy Body Dementia
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Lewy Body Disease
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Diffuse Lewy Body Disease
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Dementia With Lewy Bodies
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DLB
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Autosomal Dominant Diffuse Lewy Body Disease
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Cortical Lewy Body Disease
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Dementia, Lewy Body, Susceptibility To
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Lewy Body Dementia, Susceptibility To
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Senile Dementia Of The Lewy Body Type
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Dementia Of The Lewy Body Type
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Lbd
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Diffuse Lewy Body Disease With Gaze Palsy
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Dysphasic Dementia Hereditary
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Lewy Body Type Senile Dementia
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Lewy Body Variant Of Alzheimer Disease
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Lewy Bodies
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Lewy Body
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Dlbd - [Diffuse Lewy Body Disease]
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Clbd - [Cortical Lewy Body Disease]
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| Mutism |
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| Paget'S Disease Of Bone |
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Osteitis Deformans
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Paget Disease Of Bone
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Osseous Paget'S Disease
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Paget Disease Of Bone, Familial
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Bone Paget Disease
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Familial Paget'S Disease Of Bone
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Paget'S Bone Disease
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Familial Paget Disease Of Bone
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Paget Disease, Bone
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Pdb
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Pagets Bone Disease
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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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| Hereditary Ataxia |
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Sca
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Spinocerebellar Ataxia
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Ataxias Hereditary
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Ataxias, Hereditary
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| Fatal Familial Insomnia |
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Insomnia, Fatal Familial
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FFI
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Familial Fatal Insomnia
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Insomnia Familial Fatal
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Insomnia Fatal Familial
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Insomnia, Fatal, Familial
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Ffi - [Fatal Familial Insomnia]
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| Leukoencephalopathy, Hereditary Diffuse, With Spheroids 1 |
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Hereditary Diffuse Leukoencephalopathy With Spheroids
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Adult-Onset Leukoencephalopathy With Axonal Spheroids And Pigmented Glia
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Alsp
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Gpsc
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Subcortical Gliosis Of Neumann
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Leukoencephalopathy, Diffuse Hereditary, With Spheroids 1
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Autosomal Dominant Leukoencephalopathy With Neuroaxonal Spheroids
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Hdls
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HDLS1
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Leukoencephalopathy, Adult-Onset, With Axonal Spheroids And Pigmented Glia
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Gliosis, Familial Progressive Subcortical
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Leukoencephalopathy, Diffuse Hereditary, With Spheroids
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Pold
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Pigmentary Orthochromatic Leukodystrophy
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Hereditary Diffuse Leukoencephalopathy With Axonal Spheroids And Pigmented Glia
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Familial Progressive Subcortical Gliosis
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Leukoencephalopathy With Neuroaxonal Spheroids, Autosomal Dominant
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Dementia, Familial, Neumann Type
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Adult-Onset Leukodystrophy With Neuroaxonal Spheroids
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Hereditary Diffuse Leukoencephalopathy With Axonal Spheroids
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Neuroaxonal Leukodystrophy
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Fpsg
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Familial Dementia, Neumann Type
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Familial Dementia Neumann Type
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Leukoencephalopathy, Diffuse Hereditary, With Spheroid
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| Autosomal Dominant Cerebellar Ataxia |
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Spinocerebellar Ataxia
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Adca
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Pierre Marie Cerebellar Ataxia
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Ataxia, Spinocerebellar
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Sca
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Autosomal Dominant Spinocerebellar Ataxia
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Spinocerebellar Ataxias
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| Movement Disease |
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Movement Disorders
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Movement Disorder
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| Spinocerebellar Ataxia 10 |
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Spinocerebellar Ataxia Type 10
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SCA10
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Spinocerebellar Ataxia-10
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Ataxia, Spinocerebellar, Type 10
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| Myotonic Dystrophy 1 |
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Myotonic Dystrophy
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Dystrophia Myotonica
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Steinert Disease
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Myotonic Dystrophy Type 1
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Myotonia Atrophica
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DM1
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Congenital Myotonic Dystrophy
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Myotonia Dystrophica
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Steinert Myotonic Dystrophy
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Dystrophia Myotonica 1
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Dm
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Steinert'S Disease
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Steinert Myotonic Dystrophy Syndrome
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Myotonic Dystrophy Of Steinert
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Dystrophia Myotonica Type 1
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Myotonic Dystrophy Congenital
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Dystrophy, Myotonic, Type 1
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Dm - [Dystrophia Myotonica]
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Myotonic Muscular Dystrophy
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| Hydrocephalus |
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Hydrocephalus, Nonsyndromic, Autosomal Recessive
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Hydrocephalus, X-Linked
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Hydrocephalus Adverse Event
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Hydrocephaly Nos
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| Dystonia |
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Dystonic Disease
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Dystonic Disorder
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Dystonia Disorders
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Neuroleptic Dyskinesia
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| Disease Of Mental Health |
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Mental Health
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Mental Disorders
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| Multiple System Atrophy 1 |
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Multiple System Atrophy
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Shy-Drager Syndrome
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Msa
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MSA1
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Multiple System Atrophy 1, Susceptibility To
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Sporadic Olivopontocerebellar Atrophy
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Multisystem Atrophy
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Msa1, Susceptibility To
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Multiple System Atrophy, Susceptibility To
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Opca
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Progressive Autonomic Failure With Multiple System Atrophy
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Sds
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| Fuchs' Endothelial Dystrophy |
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Fuchs Endothelial Corneal Dystrophy
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Fuchs Endothelial Dystrophy
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Fuchs Dystrophy
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Fced
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Fuchs' Corneal Dystrophy
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Fuchs' Endothelial Corneal Dystrophy
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Fuchs Atrophy
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Fuchs Corneal Dystrophy
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Endoepithelial Corneal Dystrophy
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Fecd
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Late Hereditary Endothelial Dystrophy
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Corneal Dystrophy, Fuchs Endothelial
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Dystrophy, Corneal, Fuchs Endothelial
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Corneal Dystrophy, Fuchs' Endothelial, 1
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| Choreatic Disease |
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| Spinocerebellar Ataxia, Autosomal Recessive, With Axonal Neuropathy 2 |
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Aoa2
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Ataxia With Oculomotor Apraxia Type 2
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Scar1
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SCAN2
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Ataxia-Oculomotor Apraxia 2
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Ataxia-Ocular Apraxia 2
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Ataxia-Oculomotor Apraxia Type 2
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Scan 2
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Spinocerebellar Ataxia With Axonal Neuropathy Type 2
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Spinocerebellar Ataxia, Autosomal Recessive 1, Formerly
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Scar1, Formerly
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Autosomal Recessive Spinocerebellar Ataxia-1
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Spinocerebellar Ataxia, Autosomal Recessive, 1
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Ataxia-Ocular Apraxia-2
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Spinocerebellar Ataxia, Autosomal Recessive 1
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| Epithelial-Stromal Tgfbi Dystrophy |
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| Lattice Corneal Dystrophy |
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Familial Amyloid Neuropathy, Finnish Type
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Familial Amyloid Polyneuropathy, Type V
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| Dentatorubral-Pallidoluysian Atrophy |
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DRPLA
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Naito-Oyanagi Disease
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Haw River Syndrome
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Myoclonic Epilepsy With Choreoathetosis
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Nod
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Ataxia, Chorea, Seizures, And Dementia
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Dentatorubropallidoluysian Atrophy
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Hrs
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Naito Oyanagi Disease
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Dentatorubral Pallidoluysian Atrophy
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Dentatorubro-Pallidoluysian Atrophy
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Myoclonic Epilepsies, Progressive
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Atrophy, Pallidoluysian, Dentatorubral
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| Epilepsy, Idiopathic Generalized 2 |
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EIG2
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Epilepsy, Idiopathic Generalized, Susceptibility To, 2
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Idiopathic Generalized Epilepsy 2
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Epilepsy, Idiopathic Generalized Locus On Chromosome 14
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Epilepsy, Idiopathic Generalized, Susceptibility To, Locus On Chromosome 14
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| Specific Developmental Disorder |
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| Cortical Deafness |
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| Premature Ovarian Failure 1 |
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Ovarian Failure, Premature
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Fmr1-Related Primary Ovarian Insufficiency
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Fragile X-Associated Primary Ovarian Insufficiency
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POF1
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Pofx
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Hypergonadotropic Ovarian Failure, X-Linked
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Pof
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Primary Ovarian Insufficiency, Fragile X-Associated
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Primary Ovarian Insufficiency 1
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Ovarian Failure Premature
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Premature Ovarian Failure, X-Linked
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Fragile X Premature Ovarian Failure
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Fmr1-Related Premature Ovarian Failure
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Familial Premature Ovarian Failure
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Idiopathic Familial Premature Ovarian Failure
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Fxpoi
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X-Linked Hypergonadotropic Ovarian Failure
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Hypergonadotropic Ovarian Failure X-Linked
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Poi
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Premature Ovarian Failure X-Linked
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Primary Ovarian Insufficiency
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Premature Ovarian Failure-1
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Ovarian Failure, Premature, Type 1
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Premature Ovarian Failure, Familial
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Premature Menopause
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Primary Hypogonadism
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Turner Syndrome
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| Speech Disorder |
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| Spinocerebellar Ataxia 1 |
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Spinocerebellar Ataxia Type 1
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SCA1
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Olivopontocerebellar Atrophy I
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Opca1
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Opca4
|
Menzel Type Opca
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Schut-Haymaker Type Opca
|
Spinocerebellar Atrophy I
|
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Opca I
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Olivopontocerebellar Atrophy Iv
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Opca Iv
|
Cerebelloparenchymal Disorder I
|
|
Cpd1
|
Olivopontocerebellar Atrophy 1
|
|
Cerebelloparenchymal Disorder 1
|
Olivopontocerebellar Atrophy 4
|
|
Spinocerebellar Atrophy 1
|
Type 1 Spinocerebellar Ataxia
|
|
Spinocerebellar Ataxia-1
|
Ataxia, Spinocerebellar, Type 1
|
|
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| Parkinson Disease, Late-Onset |
|
Parkinson Disease
|
Parkinson'S Disease
|
|
PD
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PARK
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|
Parkinson Disease, Susceptibility To
|
Late Onset Parkinson'S Disease
|
|
Late Onset Parkinson Disease
|
Paralysis Agitans
|
|
Primary Parkinsonism
|
Idiopathic Parkinson Disease
|
|
Parkinson'S
|
Parkinson Disease, Late-Onset, Susceptibility To
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|
Parkinson Disease, Age Of Onset, Modifier
|
Lewy Body Parkinson Disease
|
|
Idiopathic Parkinson'S Disease
|
Pd - [Parkinson Disease]
|
|
Parkinson Disease Nos
|
Parkinson, Nos
|
|
Primary Parkinson Disease
|
|
|
| Familial Adult Myoclonic Epilepsy |
|
Benign Adult Familial Myoclonus Epilepsy
|
Bafme
|
|
Benign Adult Familial Myoclonic Epilepsy
|
Fame
|
|
Familial Cortical Myoclonic Tremor And Epilepsy
|
Fcmte
|
|
Adcme
|
Autosomal Dominant Cortical Myoclonus And Epilepsy
|
|
Fam
|
Epilepsy, Myoclonic, Familial Adult
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|
Epilepsy, Myoclonic, Benign Adult Familial, Type 2
|
|
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| Neuronal Ceroid Lipofuscinosis |
|
Hereditary Ceroid Lipofuscinosis
|
Batten Disease
|
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Ncl
|
Neuronal Ceroid-Lipofuscinoses
|
|
Lipofuscinosis, Ceroid, Neuronal
|
Juvenile Neuronal Ceroid Lipofuscinosis
|
|
Cerebromacular Dystrophy
|
Cerebromacular Degeneration
|
|
Ceroid-Lipofuscinosis
|
Ncl - [Neuronal Ceroid Lipofuscinosis]
|
|
Amaurotic Familial Idiocy
|
Amaurotic Idiocy
|
|
Amaurotic Idiot
|
Neuronal Lipofuscinosis
|
|
Pigmentary Retinal Lipoid Neuronal Heredodegeneration
|
|
|
| Neuromuscular Disease |
|
Neuromuscular Diseases
|
Neuromuscular Disorders
|
|
Neuromuscular Disorder
|
|
|
| Spinal Muscular Atrophy |
|
Sma
|
5q Sma
|
|
Proximal Sma
|
Sma-Associated Sma
|
|
Spinal Amyotrophies
|
Spinal Amyotrophy
|
|
Spinal Muscle Degeneration
|
Spinal Muscle Wasting
|
|
Muscular Atrophy Spinal
|
Atrophy, Muscular, Spinal
|
|
Hereditary Motor Neuronopathy
|
Progressive Muscular Atrophy
|
|
Sma - [Spinal Muscular Atrophy]
|
|
|
| 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
|
|
|
| Schizophrenia |
|
SCZD
|
Schizophrenia With Or Without An Affective Disorder
|
|
Schizophrenia 12
|
Schizophrenia, Susceptibility To
|
|
Schizophrenia-1
|
Dementia Praecox
|
|
Schizophrenia 1
|
|
|
| Hemochromatosis, Type 1 |
|
Hemochromatosis
|
Hemochromatosis Type 1
|
|
Hereditary Hemochromatosis
|
Hh
|
|
HFE1
|
Hfe Hemochromatosis, Modifier Of
|
|
Symptomatic Form Of Classic Hemochromatosis
|
Symptomatic Form Of Hemochromatosis Type 1
|
|
Symptomatic Form Of Hfe-Related Hereditary Hemochromatosis
|
Haemochromatosis
|
|
Iron Storage Disorder
|
Bronze Diabetes
|
|
Hereditary Haemochromatosis
|
Hlah
|
|
Hfe
|
Hemochromatosis, Hereditary
|
|
Diabetes Bronze
|
Classic Hemochromatosis
|
|
Hfe-Associated Hereditary Hemochromatosis
|
Hemochromatosis Classic
|
|
Bronzed Cirrhosis
|
Familial Hemochromatosis
|
|
Genetic Hemochromatosis
|
Hc
|
|
Pigmentary Cirrhosis
|
Primary Hemochromatosis
|
|
Troisier-Hanot-Chauffard Syndrome
|
Von Recklenhausen-Applebaum Disease
|
|
Hemochromatosis 1
|
Primary Hereditary Hemochromatosis
|
|
Bronze Cirrhosis
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| 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
|
|
|
| Peripheral Nervous System Disease |
|
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
| 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
|
|
|
| Myopathy |
|
Muscular Diseases
|
Myopathies
|
|
|
