| 疾病名称 |
别名 |
|
| Postencephalitic Parkinson Disease |
|
Postencephalitic Parkinsonism
|
Parkinson Disease, Postencephalitic
|
|
|
| Machado-Joseph Disease |
|
SCA3
|
MJD
|
|
Spinocerebellar Ataxia 3
|
Azorean Disease
|
|
Spinocerebellar Ataxia Type 3
|
Azorean Neurologic Disease
|
|
Spinopontine Atrophy
|
Nigrospinodentatal Degeneration
|
|
Spinocerebellar Atrophy
|
Spinocerebellar Atrophy Iii
|
|
Spinocerebellar Atrophy Type 3
|
Azorean Ataxia
|
|
Azorean Disease Of The Nervous System
|
Machado Disease
|
|
Nigro-Spino-Dentatal Degeneration With Nuclear Ophthalmoplegia
|
Disease, Machado-Joseph
|
|
Ataxia, Spinocerebellar
|
|
|
| Athetosis |
|
|
| 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
|
|
|
| Aphasia |
|
|
| 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
|
|
|
| Rem Sleep Behavior Disorder |
|
Rem Sleep Behaviour Disorder
|
Rapid Eye Movement Sleep Behavior Disorder
|
|
Rapid Eye Movement Sleep Behaviour Disorder
|
Rem - [Rapid Eye Movement] Behaviour Disorder
|
|
|
| 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
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| 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
|
|
|
| Neuronal Ceroid Lipofuscinosis |
|
Hereditary Ceroid Lipofuscinosis
|
Batten Disease
|
|
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
|
|
|
| Constipation |
|
|
| Kufor-Rakeb Syndrome |
|
Park9
|
Krppd
|
|
KRS
|
Pallidopyramidal Degeneration With Supranuclear Upgaze Paresis And Dementia
|
|
Autosomal Recessive Parkinson Disease 9
|
Parkinson Disease 9
|
|
Parkinson Disease 9, Autosomal Recessive, Juvenile-Onset
|
Autosomal Recessive Juvenile Onset Parkinson Disease 9
|
|
Parkinson Disease Type 9
|
Pallidopyramidal Degeneration With Supranuclear Upgaze Paresis, And Dementia
|
|
Park 9
|
Atp13a2-Related Juvenile Neuronal Ceroid Lipofuscinosis
|
|
Cln12 Disease
|
Juvenile Parkinsonism-Neuronal Ceroid Lipofuscinosis
|
|
Parkinson Disease Autosomal Recessive 9
|
|
|
| Klippel-Feil Syndrome 1, Autosomal Dominant |
|
KFS1
|
Cervical Vertebral Fusion Autosomal Dominant
|
|
Kfs
|
Cervical Vertebral Fusion, Autosomal Dominant
|
|
Cervical Vertebral Fusion Congenital
|
Congenital Klippel-Feil Segment
|
|
Fused Cervical Segments Congenital
|
Isolated Klippel-Feil Syndrome
|
|
Klippel-Feil Malformation
|
Klippel-Feil Sequence
|
|
Klippel-Feil Syndrome, Type 1, Autosomal Dominant
|
Klippel-Feil Syndrome, Autosomal Dominant
|
|
|
| Sleep Disorder |
|
Sleep Disorders
|
Non-Organic Sleep Disorder
|
|
|
| Meier-Gorlin Syndrome 3 |
|
MGORS3
|
Meier-Gorlin Syndrome, Type 3
|
|
|
| Hereditary Late-Onset Parkinson Disease |
|
Autosomal Dominant Late-Onset Parkinson Disease
|
Lopd
|
|
Hereditary Late Onset Parkinson Disease
|
|
|
| Parkinson Disease 15, Autosomal Recessive Early-Onset |
|
Parkinsonian-Pyramidal Syndrome
|
Pallidopyramidal Syndrome
|
|
Parkinson Disease 15, Autosomal Recessive
|
PARK15
|
|
Pkps
|
Pallido-Pyramidal Syndrome
|
|
Parkinson'S Disease 15
|
Autosomal Recessive Early-Onset Parkinson Disease 15
|
|
Autosomal Recessive Early-Onset Parkinson'S Disease 15
|
Pallido-Pyramidal Disease
|
|
Parkinson Disease 15
|
Parkinson Disease 15 Autosomal Recessive
|
|
Pps
|
Parkinson Disease, Type 15
|
|
|
| Intellectual Developmental Disorder, Autosomal Dominant 55, With Seizures |
|
MRD55
|
Mental Retardation, Autosomal Dominant 55, With Seizures
|
|
Autosomal Dominant Mental Retardation 55
|
Autosomal Dominant Intellectual Developmental Disorder 55
|
|
Autosomal Dominant Intellectual Developmental Disorder-55 With Seizures
|
Mental Retardation, Autosomal Dominant, Type 55, With Seizures
|
|
|
| Hereditary Spastic Paraplegia |
|
Familial Spastic Paraplegia
|
Hereditary Spastic Paraparesis
|
|
Strumpell-Lorrain Disease
|
Hsp
|
|
Spg
|
Strümpell-Lorrain Disease
|
|
Spastic Paraplegia, Hereditary
|
French Settlement Disease
|
|
Strumpell-Lorrain Syndrome
|
Fsp
|
|
Familial Spastic Paraparesis
|
Spastic Paraplegia, Familial
|
|
Spastic Paraplegia Hereditary
|
Spastic Paraplegia 3, Autosomal Dominant
|
|
Spastic Paraparesis
|
Hereditary Spastic Paralysis
|
|
Familial Spastic Paralysis
|
Hereditary Spastic Ataxia
|
|
|
| Rheumatoid Arthritis |
|
RA
|
Arthritis, Rheumatoid
|
|
Rheumatoid Arthritis, Susceptibility To
|
Arthritis Or Polyarthritis, Rheumatic
|
|
Atrophic Arthritis
|
Rheumatism Arthritis
|
|
Rheumatoid Polyarthritis
|
|
|
| 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
|
|
|
| Parkinson Disease 1, Autosomal Dominant |
|
Autosomal Dominant Parkinson Disease 1
|
PARK1
|
|
Parkinson Disease 1
|
Parkinson'S Disease 1
|
|
Atypical Parkinson Disease
|
Parkinson Disease 1, Autosomal Dominant Lewy Body
|
|
Autosomal Dominant Parkinson'S Disease 1
|
Lewy Body Parkinsonism
|
|
Parkinson Disease Autosomal Dominant 1
|
Parkinson Disease Familial Type 1
|
|
Parkinson Disease, Type 1
|
Parkinson Disease, Familial, Type 1
|
|
|
| Ciliary Dyskinesia, Primary, 43 |
|
CILD43
|
Primary Ciliary Dyskinesia 43
|
|
Ciliary Dyskinesia, Primary, 43, With Or Without Situs Inversus
|
Primary Ciliary Dyskinesia 43 With Or Without Situs Inversus
|
|
Ciliary Dyskinesia, Primary, 43 With Or Without Situs Inversus
|
|
|
| Movement Disease |
|
Movement Disorders
|
Movement Disorder
|
|
|
| Early-Onset Parkinson'S Disease |
|
Early-Onset Parkinson Disease
|
|
|
| Parkinson Disease 2, Autosomal Recessive Juvenile |
|
Young-Onset Parkinson Disease
|
PARK2
|
|
Pdj
|
Autosomal Recessive Juvenile Parkinson Disease 2
|
|
Epdf
|
Parkinson Disease, Juvenile, Type 2
|
|
Parkinson'S Disease 2
|
Autosomal Recessive Juvenile Parkinson Disease
|
|
Early-Onset Parkinson Disease
|
Parkinson Disease 2
|
|
Parkinson Disease, Juvenile, Autosomal Recessive
|
Parkinsonism, Early-Onset, With Diurnal Fluctuation
|
|
Autosomal Recessive Juvenile Parkinson'S Disease 2
|
Jp
|
|
Juvenile Parkinsonism
|
Parkinson Disease Autosomal Recessive, Early Onset
|
|
Parkinsonism, Early Onset, With Diurnal Fluctuation
|
Yopd
|
|
Autosomal Recessive Early-Onset Parkinson Disease Type 2
|
Chromosome 6-Linked Autosomal Recessive Parkinsonism
|
|
Early-Onset Parkinsonism With Diurnal Fluctuation
|
Parkinsonism Young Adult Onset
|
|
Parkinson Disease, Type 2
|
Parkinsonism, Juvenile
|
|
|
| Vascular Parkinsonism |
|
|
| 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]
|
|
|
| 3-Methylglutaconic Aciduria, Type Iii |
|
Optic Atrophy
|
3-Methylglutaconic Aciduria Type 3
|
|
Costeff Syndrome
|
Mga3
|
|
Costeff Optic Atrophy Syndrome
|
Optic Atrophy Plus Syndrome
|
|
Infantile Optic Atrophy With Chorea And Spastic Paraplegia
|
3-Methylglutaconic Aciduria Type Iii
|
|
Autosomal Recessive Optic Atrophy Plus Syndrome
|
Autosomal Recessive Optic Atrophy Type 3
|
|
Opa3 Defect
|
MGCA3
|
|
Mga, Type Iii
|
Iraqi Jewish Optic Atrophy Plus
|
|
Mga Type Iii
|
Optic Atrophy, Infantile, With Chorea And Spastic Paraplegia
|
|
Iraqi-Jewish 'Optic Atrophy Plus'
|
Optic Atrophy 3, Autosomal Recessive
|
|
Opa3, Autosomal Recessive
|
Opa3-Related 3-Methylglutaconic Aciduria
|
|
Iraqi-Jewish Optic Atrophy Plus
|
Atrophy Of Optic Disc
|
|
3-Alpha Methylglutaconic Aciduria Type Iii
|
Optic Atrophy 3
|
|
Optic Atrophy Infantile With Chorea And Spastic Paraplegia
|
Autosomal Recessive Opa3
|
|
Autosomal Recessive Optic Atrophy 3
|
3-Methylglutaconic Aciduria 3
|
|
3-Alpha-Methylglutaconic Aciduria Type 3
|
Optic Atrophy 3 Autosomal Recessive
|
|
Atrophy, Optic
|
Atrophy, Optic, Plus Syndrome
|
|
Optic Nerve Atrophy
|
Primary Optic Atrophy
|
|
Oa - [Optic Atrophy]
|
Second Cranial Nerve Atrophy
|
|
Second Cranium Nerve Atrophy
|
|
|
| Parkinson Disease, Late-Onset |
|
Parkinson Disease
|
Parkinson'S Disease
|
|
PD
|
PARK
|
|
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
|
|
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
|
|
|
| Parkinson Disease 3, Autosomal Dominant |
|
Parkinson Disease 3
|
PARK3
|
|
Parkinson Disease 3, Autosomal Dominant Lewy Body
|
Parkinson'S Disease 3
|
|
Autosomal Dominant Lewy Body Parkinson Disease 3
|
Autosomal Dominant Parkinson Disease 3
|
|
Parkinson Disease Type 3
|
Autosomal Dominant Parkinson Disease
|
|
Parkinson Disease, Autosomal Dominant
|
Parkinson Disease, Familial, Type 1
|
|
|
| Choreatic Disease |
|
|
| 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
|
|
|
| Parkinson Disease 8, Autosomal Dominant |
|
Parkinson Disease 8
|
Autosomal Dominant Parkinson Disease 8
|
|
PARK8
|
Parkinson'S Disease 8
|
|
Autosomal Dominant Parkinson'S Disease 8
|
Parkinson Disease-8
|
|
Parkinson Disease, Type 8, Autosomal Dominant
|
|
|
| Pick Disease Of Brain |
|
Pick Disease
|
Pick Disease Of The Brain
|
|
Lobar Atrophy Of Brain
|
Dementia With Lobar Atrophy And Neuronal Cytoplasmic Inclusions
|
|
Pick'S Disease
|
Behavioral Variant Of Frontotemporal Dementia
|
|
Dementia In Pick'S Disease
|
Lobar Atrophy Of The Brain
|
|
Bvftd
|
Bv-Ftd
|
|
PIDB
|
Picks Disease
|
|
|
| Parkinsonism |
|
Parkinsonism-Plus
|
Idiopathic Parkinsonism
|
|
Primary Parkinsonism
|
Paralysis Agitans Syndrome
|
|
Parkinsonian Syndrome
|
Trembling Paralysis
|
|
Paralysis Agitans
|
Shaking Palsy
|
|
Shaking Paralysis
|
|
|
| Cerebellar Disease |
|
Cerebellar Diseases
|
Cerebellar Dysfunction
|
|
Cerebellar Abnormality
|
Cerebellar Disorders
|
|
|
| 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
|
|
|
| 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]
|
|
|
| Gaucher'S Disease |
|
Gaucher Disease
|
Kerasin Thesaurismosis
|
|
Glucocerebrosidase Deficiency
|
Glucosylceramidase Deficiency
|
|
Acid Beta-Glucosidase Deficiency
|
Glucosylceramide Beta-Glucosidase Deficiency
|
|
Acute Cerebral Gaucher Disease
|
Cerebroside Lipidosis Syndrome
|
|
Gaucher Splenomegaly
|
Glucocerebrosidosis
|
|
Glucosyl Cerebroside Lipidosis
|
Kerasin Lipoidosis
|
|
Lipoid Histiocytosis
|
Glocucerebrosidase Deficiency
|
|
Sphingolipidosis 1
|
Gaucher Syndrome
|
|
Gauchers Disease
|
Gd
|
|
Glucosylceramide Lipidosis
|
Kerasin Histiocytosis
|
|
Gaucher Disease, Type 1
|
Gaucher Disease, Type 2
|
|
|
| Tremor |
|
Medicament-Induced Tremor
|
Medication-Induced Postural Tremor
|
|
|
| Mitochondrial Complex I Deficiency, Nuclear Type 1 |
|
Mitochondrial Complex I Deficiency
|
Nadh:Q(1) Oxidoreductase Deficiency
|
|
MC1DN1
|
Nadh-Coenzyme Q Reductase Deficiency
|
|
Isolated Mitochondrial Respiratory Chain Complex I Deficiency
|
Isolated Nadh-Coenzyme Q Reductase Deficiency
|
|
Isolated Nadh-Coq Reductase Deficiency
|
Isolated Nadh-Ubiquinone Reductase Deficiency
|
|
Mitochondrial Nadh Dehydrogenase Component Of Complex I, Deficiency Of
|
Nuclear Type Mitochondrial Complex I Deficiency 1
|
|
Isolated Complex I Deficiency
|
Complex 1 Mitochondrial Respiratory Chain Deficiency
|
|
Nadh Coenzyme Q Reductase Deficiency
|
Complex I Mitochondrial Respiratory Chain Deficiency
|
|
Deficiency Of Mitochondrial Nadh Dehydrogenase Component Of Complex I
|
Nadh:Ubiquinone Oxidoreductase Deficiency
|
|
Complex I, Mitochondrial Respiratory Chain, Deficiency Of
|
|
|
| Autosomal Dominant Cerebellar Ataxia |
|
Spinocerebellar Ataxia
|
Adca
|
|
Pierre Marie Cerebellar Ataxia
|
Ataxia, Spinocerebellar
|
|
Sca
|
Autosomal Dominant Spinocerebellar Ataxia
|
|
Spinocerebellar Ataxias
|
|
|
| Von Economo'S Disease |
|
Encephalitis Lethargica
|
Von Economo Encephalitis
|
|
Von Economo Disease
|
|
|
| Supranuclear Palsy, Progressive, 1 |
|
Progressive Supranuclear Palsy
|
Steele-Richardson-Olszewski Syndrome
|
|
Supranuclear Palsy, Progressive
|
Psp
|
|
Progressive Supranuclear Ophthalmoplegia
|
PSNP1
|
|
Familial Progressive Supranuclear Palsy
|
Richardson'S Syndrome
|
|
Psp Syndrome
|
Progressive Supranuclear Palsy 1
|
|
Supranuclear Palsy Progressive
|
Ophthalmoplegia, Supranuclear, Progressive
|
|
Steele-Richardson-Olszewksi Syndrome
|
|
|
| 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
|
|
|
| Gaucher Disease, Type I |
|
Glucocerebrosidase Deficiency
|
Acid Beta-Glucosidase Deficiency
|
|
Gba Deficiency
|
GD1
|
|
Gd I
|
Gaucher Disease, Noncerebral Juvenile
|
|
Gaucher Disease Type 1
|
Gaucher Disease Type I
|
|
Gaucher'S Disease Type I
|
Gaucher Disease
|
|
Gd 1
|
Non-Cerebral Juvenile Gaucher Disease
|
|
GD
|
Gaucher Disease 1
|
|
Adult Non-Neuronopathic Gaucher Disease
|
Noncerebral Juvenile Gaucher Disease
|
|
Type 1 Gaucher Disease
|
Gaucher Disease, Type 1
|
|
|
| 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
|
|
|
| Striatonigral Degeneration |
|
|
| Toxic Encephalopathy |
|
Neurotoxicity
|
Neurotoxicity Syndromes
|
|
Neurotoxicity Syndrome
|
Encephalopathy, Toxic
|
|
|
| Leprosy 3 |
|
Leprosy
|
Leprosy, Susceptibility To, 3
|
|
Hansen'S Disease
|
Leprosy, Susceptibility To
|
|
Hansen Disease
|
Infection Due To Mycobacterium Leprae
|
|
LPRS3
|
Leprosy, Type 3
|
|
Anaesthesia Leprosy
|
Anaesthetic Leprosy
|
|
Maculoanaesthetic Leprosy
|
Macular Leprosy
|
|
Leprosy Unspecified
|
|
|
| Sphingolipidosis |
|
|
