| Diseases |
Alias |
|
| Gerstmann Syndrome |
|
Aphasia-Angular Gyrus Syndrome
|
Developmental Gerstmann Syndrome
|
|
Gs
|
Gerstmann Badal Syndrome
|
|
Gerstmann Tetrad
|
Gerstmann'S Syndrome
|
|
Developmental Gerstmann'S Syndrome
|
|
|
| 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
|
|
|
| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 7 |
|
Ftd3
|
Frontotemporal Dementia, Chromosome 3-Linked
|
|
Amyotrophic Lateral Sclerosis, Chmp2b-Related
|
Chromosome 3-Linked Frontotemporal Dementia
|
|
FTDALS7
|
Chmp2b-Related Frontotemporal Dementia
|
|
Amyotrophic Lateral Sclerosis 17, Formerly
|
Als17, Formerly
|
|
Amyotrophic Lateral Sclerosis Type 17
|
Dtm1
|
|
Ftd-3
|
Ftd-Chmp2b
|
|
Als17
|
Amyotrophic Lateral Sclerosis 17
|
|
Sclerosis, Lateral, Amyotrophic, Type 17
|
Dementia, Frontotemporal, Chromosome 3-Linked
|
|
|
| Dysgraphia |
|
|
| Parkinson-Dementia Syndrome |
|
Progressive Supranuclear Palsy-Parkinsonism Syndrome
|
Supranuclear Palsy, Progressive Atypical
|
|
Progressive Supranuclear Palsy Atypical
|
Atypical Psp
|
|
Psp-P
|
Psp-Parkinsonism
|
|
Atypical Progressive Supranuclear Palsy Syndrome
|
Atypical Psp Syndrome
|
|
PARDE
|
Steele-Richardson-Olszewski Syndrome Atypical
|
|
Supranuclear Palsy Progressive 1 Atypical
|
Supranuclear Palsy, Progressive, 1, Atypical
|
|
|
| Parkinsonism |
|
Parkinsonism-Plus
|
Idiopathic Parkinsonism
|
|
Primary Parkinsonism
|
Paralysis Agitans Syndrome
|
|
Parkinsonian Syndrome
|
Trembling Paralysis
|
|
Paralysis Agitans
|
Shaking Palsy
|
|
Shaking Paralysis
|
|
|
| Corticobasal Degeneration |
|
|
| Chromosomal Disease |
|
Chromosomal Disorders
|
Congenital Chromosomal Disease
|
|
|
| Vascular Dementia |
|
Dementia, Vascular
|
Multi Infarct Dementia
|
|
Multifocal Dementia
|
Dementia Vascular
|
|
Vascular Dementia, Susceptibility To
|
Dementia, Multi-Infarct
|
|
Multi-Infarct Dementia
|
|
|
| Progressive Supranuclear Palsy-Pure Akinesia With Gait Freezing Syndrome |
|
Psp-Pagf
|
Psp-Pure Akinesia With Gait Freezing
|
|
|
| Chromosomal Duplication Syndrome |
|
|
| 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
|
|
|
| Prosopagnosia |
|
|
| 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
|
|
|
| Writing Disorder |
|
|
| 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]
|
|
|
| Paralytic Lagophthalmos |
|
|
| Schizophrenia |
|
SCZD
|
Schizophrenia With Or Without An Affective Disorder
|
|
Schizophrenia 12
|
Schizophrenia, Susceptibility To
|
|
Schizophrenia-1
|
Dementia Praecox
|
|
Schizophrenia 1
|
|
|
| Nominal Aphasia |
|
|
| Hereditary Late-Onset Parkinson Disease |
|
Autosomal Dominant Late-Onset Parkinson Disease
|
Lopd
|
|
Hereditary Late Onset Parkinson Disease
|
|
|
| Myxoid Chondrosarcoma |
|
|
| Prion Disease |
|
Spongiform Encephalopathy
|
Transmissible Spongiform Encephalopathies
|
|
Prion Diseases
|
Prion Disease Pathway
|
|
Transmissible Spongiform Encephalopathy
|
Prion Induced Disorder
|
|
Prion Protein Disease
|
Inherited Human Transmissible Spongiform Encephalopathies
|
|
Prion Protein Diseases
|
Prion-Associated Disorders
|
|
Prion-Induced Disorders
|
Transmissible Dementias
|
|
Tses
|
Human Prion Disease
|
|
Tse
|
Encephalopathy, Transmissible Spongiform
|
|
Prion Disease, Susceptibility To
|
Spongiform Encephalopathies
|
|
Human Transmissible Spongiform Encephalopathies, Inherited
|
|
|
| Apperceptive Agnosia |
|
|
| Hydrocephalus |
|
Hydrocephalus, Nonsyndromic, Autosomal Recessive
|
Hydrocephalus, X-Linked
|
|
Hydrocephalus Adverse Event
|
Hydrocephaly Nos
|
|
|
| Postencephalitic Parkinson Disease |
|
Postencephalitic Parkinsonism
|
Parkinson Disease, Postencephalitic
|
|
|
| Capgras Syndrome |
|
|
| Amyotrophic Lateral Sclerosis 3 |
|
ALS3
|
Amyotrophic Lateral Sclerosis Type 3
|
|
|
| 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
|
|
|
| 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]
|
|
|
| Huntington Disease |
|
Huntington'S Disease
|
Huntington Chorea
|
|
HD
|
Huntington'S Chorea
|
|
Huntington Chronic Progressive Hereditary Chorea
|
Juvenile Huntington Disease
|
|
Chronic Progressive Chorea
|
Chronic Progressive Hereditary Chorea
|
|
Hc - [Huntington Chorea]
|
Hereditary Chorea
|
|
Progressive Hereditary Chorea
|
|
|
| Myotonic Dystrophy 1 |
|
Myotonic Dystrophy
|
Dystrophia Myotonica
|
|
Steinert Disease
|
Myotonic Dystrophy Type 1
|
|
Myotonia Atrophica
|
DM1
|
|
Congenital Myotonic Dystrophy
|
Myotonia Dystrophica
|
|
Steinert Myotonic Dystrophy
|
Dystrophia Myotonica 1
|
|
Dm
|
Steinert'S Disease
|
|
Steinert Myotonic Dystrophy Syndrome
|
Myotonic Dystrophy Of Steinert
|
|
Dystrophia Myotonica Type 1
|
Myotonic Dystrophy Congenital
|
|
Dystrophy, Myotonic, Type 1
|
Dm - [Dystrophia Myotonica]
|
|
Myotonic Muscular Dystrophy
|
|
|
| Subjective Cognitive Decline |
|
|
| Cerebellar Disease |
|
Cerebellar Diseases
|
Cerebellar Dysfunction
|
|
Cerebellar Abnormality
|
Cerebellar Disorders
|
|
|
| Cerebral Amyloid Angiopathy, Cst3-Related |
|
Cerebral Amyloid Angiopathy
|
Hereditary Cerebral Hemorrhage With Amyloidosis
|
|
Hchwa
|
Cerebral Amyloid Angiopathy, Familial
|
|
Hereditary Cystatin C Amyloid Angiopathy
|
Amyloidosis, Cerebroarterial, Icelandic Type
|
|
Amyloidosis Vi
|
Cerebral Hemorrhage, Hereditary, With Amyloidosis
|
|
Cst3-Related Cerebral Amyloid Angiopathy
|
Cerebral Hemorrhage, Hereditary, With Amyloidosis, Icelandic Variant
|
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Icelandic Variant
|
Caa, Familial
|
|
Cerebral Amyloid Angiopathy, Genetic
|
Acys Amyloidosis
|
|
Cst3-Related Amyloidosis
|
Cystatin Amyloidosis
|
|
Hchwa, Icelandic Type
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Icelandic Type
|
|
Amyloidosis 6
|
AMYL6
|
|
Acys
|
Caa
|
|
Cerebral Amyloid Angiopathy Cst3-Related
|
Cerebroarterial Amyloidosis Icelandic Type
|
|
Cystatin C Amyloidosis
|
Hccaa
|
|
Hchwai
|
Hchwa-I
|
|
Hereditary Cerebral Hemorrhage With Amyloidosis Icelandic Type
|
Cerebral Amyloid Angiopathy Familial
|
|
Angiopathy, Amyloid, Cerebral, Cst3-Related
|
Hereditary Cerebral Amyloid Angiopathy, Icelandic Type
|
|
Familial Cerebral Amyloid Angiopathy
|
Cerebral Amyloid Angiopathy, Hereditary
|
|
|
| Autosomal Dominant Cerebellar Ataxia |
|
Spinocerebellar Ataxia
|
Adca
|
|
Pierre Marie Cerebellar Ataxia
|
Ataxia, Spinocerebellar
|
|
Sca
|
Autosomal Dominant Spinocerebellar Ataxia
|
|
Spinocerebellar Ataxias
|
|
|
| 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
|
|
|
| Vascular Parkinsonism |
|
|
| Arteriolosclerosis |
|
|
| Normal Pressure Hydrocephalus |
|
Low Pressure Hydrocephalus
|
Hydrocephalus Normal Pressure
|
|
Hydrocephalus, Normal Pressure
|
Normal Pressure Hydrocephalus Nos
|
|
Nph - [Normal Pressure Hydrocephalus]
|
Normal Pressure Hydrocephaly
|
|
|
| Specific Developmental Disorder |
|
|
| Associative Agnosia |
|
|
| Alzheimer Disease 10 |
|
Ad10
|
Alzheimer Disease-10
|
|
Alzheimer'S Disease 10
|
Alzheimer Disease, Familial, 10
|
|
Alzheimer Disease Familial 10
|
Alzheimer'S Disease 10, Early Onset
|
|
|
| Coenzyme Q10 Deficiency, Primary, 1 |
|
COQ10D1
|
Ubiquinone Deficiency 1
|
|
Coenzyme Q Deficiency 1
|
Coq Deficiency 1
|
|
Coq10 Deficiency, Primary, 1
|
Primary Coenzyme Q10 Deficiency 1
|
|
Primary Coq10 Deficiency 1
|
Coenzyme Q10 Deficiency, Primary, Type 1
|
|
|
| Inclusion Body Myositis |
|
Ibm
|
Sporadic Inclusion Body Myositis
|
|
Myositis, Inclusion Body
|
Inflammatory Myopathy
|
|
Inflammatory Myopathies
|
Sibm
|
|
Myositis Inclusion Body
|
Nonaka Myopathy
|
|
Inclusion Body Myopathy, Autosomal Recessive
|
Inclusion Body Myopathy, Autosomal Dominant
|
|
Myositis
|
Inclusion Body Myopathy, Sporadic
|
|
|
| Ideomotor Apraxia |
|
Apraxia, Ideomotor
|
Classic Apraxia
|
|
Ideomotor Dyspraxia
|
Limb-Kinetic Apraxia
|
|
Transcortical Apraxia
|
|
|
| Alzheimer Disease 9 |
|
AD9
|
Alzheimer'S Disease 9
|
|
Alzheimer Disease 9, Susceptibility To
|
Alzheimer Disease 9, Late-Onset
|
|
Alzheimer'S Disease 9, Late Onset
|
{Alzheimer Disease 9, Susceptibility To}
|
|
|
| Mutism |
|
|
| 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
|
|
|
| Cortical Deafness |
|
|
| Stroke, Ischemic |
|
Cerebral Infarction
|
Stroke
|
|
Ischemic Stroke
|
Cerebrovascular Accident
|
|
Cerebral Infarction, Susceptibility To
|
Stroke, Ischemic, Susceptibility To
|
|
Cerebral Infarct
|
Ischemic Stroke, Susceptibility To
|
|
Stroke, Susceptibility To
|
Cva - Cerebral Infarction
|
|
ISCHSTR
|
Ischemic Cerebrovascular Accident
|
|
|
| Neuroblastoma |
|
Nb
|
Neuroblastoma, Susceptibility To
|
|
Neuroblastomas
|
Central Neuroblastoma
|
|
|
| Speech Disorder |
|
|
| Echolalia |
|
|
| 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
|
|
|
| Amyloidosis |
|
Amyloid Disease
|
Amyloid
|
|
Amyloid Degeneration
|
Amyloidosis Nos
|
|
Amyloid Deposition
|
Amyloid Infiltration
|
|
Idiopathic Amyloidosis
|
Hyaloid Degeneration
|
|
Lardaceous Degeneration
|
|
|
| Hereditary Ataxia |
|
Sca
|
Spinocerebellar Ataxia
|
|
Ataxias Hereditary
|
Ataxias, Hereditary
|
|
|
| Agraphia |
|
|
| 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
|
|
|
| Congenital Nervous System Abnormality |
|
Congenital Neurologic Anomaly
|
Congenital Nervous System Disorder
|
|
|
| Down Syndrome |
|
Trisomy 21
|
Complete Trisomy 21 Syndrome
|
|
Down'S Syndrome
|
Trisomy 21 Syndrome
|
|
Down'S Syndrome - Trisomy 21
|
Downs Syndrome
|
|
G Trisomy
|
47,Xx,+21
|
|
47,Xy,+21
|
Trisomy G
|
|
Down Syndrome, Susceptibility To
|
Chromosome 21 Trisomy
|
|
Trisomy 21 Nos
|
Abnormal Autosomes 21
|
|
|
| Central Nervous System Disease |
|
CNS
|
Cns Diseases
|
|
Central Nervous System Diseases
|
Cns Disorder
|
|
|
| Cerebral Degeneration |
|
Brain Degeneration
|
Degenerative Brain Disorder
|
|
|
| Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone With Or Without Frontotemporal Dementia 2 |
|
Ibmpfd2
|
Msp2
|
|
Multisystem Proteinopathy 2
|
|
|
| Pseudobulbar Palsy |
|
|
| 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
|
|
|
| Akinetic Mutism |
|
|
| 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
|
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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
|
Wld
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Ppnd
|
Dementia, Frontotemporal, With Or Without Parkinsonism
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Semantic Primary Progressive Aphasia
|
Semantic Variant Ppa
|
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Wilhemsen-Lynch Disease
|
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
|
Ftd - [Frontotemporal Dementia]
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Temple Dementia
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Frontal Lobe Dementia
|
|
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| Nervous System Disease |
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Abnormality Of The Nervous System
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Nervous System Diseases
|
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Nervous System Disorder
|
|
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| Alzheimer Disease, Familial, 1 |
|
Alzheimer Disease
|
Alzheimer'S Disease
|
|
Presenile And Senile Dementia
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AD1
|
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Alzheimer Disease, Susceptibility To
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Alzheimer Disease, Late-Onset, Susceptibility To
|
|
Alzheimer Disease 1, Familial
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AD
|
|
Familial Alzheimer Disease
|
Alzheimer Disease, Late-Onset
|
|
Alzheimers Dementia
|
Alzheimer Dementia
|
|
Alzheimer Sclerosis
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Alzheimer Syndrome
|
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Alzheimer-Type Dementia
|
Dat
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Primary Senile Degenerative Dementia
|
Sdat
|
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Alzheimer Disease 1
|
Autosomal Dominant Alzheimer Disease
|
|
Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy
|
Late Onset Alzheimer Disease
|
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Alzheimers Disease
|
Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy
|
|
Late-Onset Alzheimers Disease
|
Alzheimer'S Disease Pathway Kegg
|
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Dementia Due To Alzheimer'S Disease
|
Alzheimer Disease Type 1
|
|
Alzheimers
|
|
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| Neuronal Ceroid Lipofuscinosis |
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Hereditary Ceroid Lipofuscinosis
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Batten Disease
|
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Ncl
|
Neuronal Ceroid-Lipofuscinoses
|
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Lipofuscinosis, Ceroid, Neuronal
|
Juvenile Neuronal Ceroid Lipofuscinosis
|
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Cerebromacular Dystrophy
|
Cerebromacular Degeneration
|
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Ceroid-Lipofuscinosis
|
Ncl - [Neuronal Ceroid Lipofuscinosis]
|
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Amaurotic Familial Idiocy
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Amaurotic Idiocy
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Amaurotic Idiot
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Neuronal Lipofuscinosis
|
|
Pigmentary Retinal Lipoid Neuronal Heredodegeneration
|
|
|
| Progressive Non-Fluent Aphasia |
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Non-Fluent Variant Ppa
|
Non-Fluent Primary Progressive Aphasia
|
|
Agramatic Variant Of Ppa
|
Agramatic Variant Of Primary Progressive Aphasia
|
|
Progressive Nonfluent Aphasia
|
Primary Progressive Non Fluent Aphasia
|
|
Primary Progressive Nonfluent Aphasia
|
|
|
| Lumbosacral Plexus Lesion |
|
Lumbosacral Plexus Lesions
|
|
|
| Tremor |
|
Medicament-Induced Tremor
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Medication-Induced Postural Tremor
|
|
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| Perry Syndrome |
|
Parkinsonism With Alveolar Hypoventilation And Mental Depression
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PERRYS
|
|
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| Diabetes Mellitus |
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| Mild Cognitive Impairment |
|
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| Anosognosia |
|
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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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|
|
| Binswanger'S Disease |
|
Multi-Infarct Dementia
|
Dementia Multi-Infarct
|
|
Binswanger Disease
|
|
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| Scrapie |
|
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| Visual Agnosia |
|
|
| Progressive Supranuclear Palsy-Corticobasal Syndrome |
|
Psp-Cbs
|
Psp-Corticobasal Syndrome
|
|
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| Restless Legs Syndrome |
|
Wed
|
Willis-Ekbom Disease
|
|
Restless Leg Syndrome
|
Ekbom Syndrome
|
|
Wittmaack-Ekbom Syndrome
|
Willis Ekbom Disease
|
|
Ekbom'S Syndrome
|
Rls
|
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Restless Legs
|
Restless Legs Syndrome, Susceptibility To
|
|
|
| Peripheral Nervous System Disease |
|
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
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Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
| Alcohol Dependence |
|
Alcoholism
|
Alcohol Dependence, Susceptibility To
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Aerodigestive Tract Cancer, Squamous Cell, Alcohol-Related, Protection Against
|
Alcohol Dependence, Protection Against
|
|
Alcoholism, Susceptibility To
|
Alcoholic Intoxication, Chronic
|
|
Pharyngeal Neoplasms
|
Chronic Alcoholism
|
|
Dipsomania
|
Alcohol Addiction
|
|
Ethanol Dependence
|
Chronic Ethanolism
|
|
Chronic Alcoholic Disease Nos
|
Alcoholic Disease Nos
|
|
Alcoholic
|
|
|
| Niemann-Pick Disease, Type C1 |
|
Niemann-Pick Disease, Type C
|
NPC1
|
|
Niemann-Pick Disease, Type D
|
Niemann-Pick Disease Type C1
|
|
Niemann-Pick Disease With Cholesterol Esterification Block
|
Niemann-Pick Disease, Subacute Juvenile Form
|
|
Neurovisceral Storage Disease With Vertical Supranuclear Ophthalmoplegia
|
Npc
|
|
Niemann-Pick Disease, Chronic Neuronopathic Form
|
Niemann-Pick Disease Without Sphingomyelinase Deficiency
|
|
Niemann-Pick Disease Type C
|
Niemann-Pick Disease Type D
|
|
Niemann-Pick C1 Disease
|
Niemann-Pick Disease C1
|
|
Niemann-Pick Disease Chronic Neuronopathic Form
|
Niemann-Pick Disease Nova Scotian Type
|
|
Niemann-Pick Disease Subacute Juvenile Form
|
Niemann-Pick Disease Type Ii
|
|
Niemann-Picks Disease Type C
|
|
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| Pick Disease Of Brain |
|
Pick Disease
|
Pick Disease Of The Brain
|
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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
|
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PIDB
|
Picks Disease
|
|
|
| Bipolar Disorder |
|
Bipolar Depression
|
Manic Disorder
|
|
Depression, Bipolar
|
Bipolar Disorder Manic Phase
|
|
Depressive-Manic Psych.
|
Manic Bipolar Affective Disorder
|
|
Manic Bipolar I Disorder
|
Manic Depression
|
|
Manic Depressive Disorder
|
Mixed Bipolar Disorder
|
|
Bipolar Affective Disorder
|
Bipolar Affective Psychosis
|
|
Bipolar Spectrum Disorder
|
Manic Depressive Illness
|
|
Depression Bipolar
|
Bipolar Disorder, Mixed
|
|
Major Affective Disorder
|
Major Affective Disorder 1
|
|
Major Affective Disorder 2
|
|
|
| Finger Agnosia |
|
|
| Toxic Encephalopathy |
|
Neurotoxicity
|
Neurotoxicity Syndromes
|
|
Neurotoxicity Syndrome
|
Encephalopathy, Toxic
|
|
|
| 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
|
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Autosomal Dominant Intellectual Developmental Disorder-55 With Seizures
|
Mental Retardation, Autosomal Dominant, Type 55, With Seizures
|
|
|
| Alzheimer Disease 11 |
|
Ad11
|
Alzheimer'S Disease 11
|
|
Alzheimer Disease, Familial, 11
|
Alzheimer Disease-11
|
|
Alzheimer'S Disease 11, Late Onset
|
|
|
| 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
|
|
|
| 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
|
|
|
| Movement Disease |
|
Movement Disorders
|
Movement Disorder
|
|
|
| Apraxia |
|
|
| Choreatic Disease |
|
|
| Speech And Communication Disorders |
|
Language Disorder
|
Communication Disorder
|
|
Language Disorders
|
Communication Disorders
|
|
Speech Language Disorder
|
Speech-Language Disorder
|
|
Communication Impairment
|
Speech And Language Disorder
|
|
|
| Kuru |
|
Kuru, Susceptibility To
|
Kuru Encephalopathy
|
|
Kuru Encephalitis
|
Kuru Disease
|
|
|
| Myositis |
|
Idiopathic Inflammatory Myopathy
|
Idiopathic Inflammatory Myositis
|
|
Iim
|
Imm
|
|
Idiopathic Inflammatory Myopathies
|
Myopathy, Familial Idiopathic Inflammatory
|
|
Inflammatory Disorder Of Muscle
|
Idiopathic Inflammatory Myopathy, Familial
|
|
Inflammatory Myopathy, Idiopathic
|
Myopathies Idiopathic Inflammatory
|
|
Familial Idiopathic Inflammatory Myopathy
|
|
|
| Disease Of Mental Health |
|
Mental Health
|
Mental Disorders
|
|
|
| Amnestic Disorder |
|
Amnesia
|
Amnestic Syndrome
|
|
Korsakoff'S Psychosis Or Syndrome
|
Amnesic Syndrome
|
|
Amnestic Disorder In Conditions Classified Elsewhere
|
Korsakoff Psychosis Or Syndrome, Nonalcoholic
|
|
Nonalcoholic Organic Amnesic Syndrome
|
Organic Amnesic Syndrome
|
|
|
| Koolen-De Vries Syndrome |
|
KDVS
|
17q21.31 Microdeletion Syndrome
|
|
Microdeletion 17q21.31 Syndrome
|
Chromosome 17q21.31 Deletion Syndrome
|
|
Koolen De Vries Syndrome
|
Kansl1-Related Intellectual Disability Syndrome
|
|
Chromosome 17q21.31 Microdeletion Syndrome
|
Monosomy 17q21.31
|
|
17q21.31 Deletion Syndrome
|
Koolen Syndrome
|
|
Del(17)(Q21.31)
|
|
|
| Demyelinating Disease |
|
Demyelinating Diseases
|
Demyelinating Disorder
|
|
|
| Progressive Supranuclear Palsy-Progressive Non-Fluent Aphasia Syndrome |
|
Psp-Aos
|
Psp-Pnfa
|
|
Progressive Supranuclear Palsy-Apraxia Of Speech Syndrome
|
|
|
| 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
|
|
|
| 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
|
|
|
| Miyoshi Muscular Dystrophy |
|
Distal Myopathy
|
Distal Muscular Dystrophy
|
|
Miyoshi Myopathy
|
Distal Myopathies
|
|
Dystrophy, Muscular, Miyoshi
|
Myopathy, Distal
|
|
Distal Muscular Dystrophies
|
|
|
| Neuritis |
|
|
| Simultanagnosia |
|
|
| Muscular Atrophy |
|
Muscle Wasting
|
Amyotrophia
|
|
Wasting - Muscle
|
Skeletal Muscle Atrophy
|
|
|
| Communicating Hydrocephalus |
|
Acquired Communicating Hydrocephalus
|
|
|
| Classic Progressive Supranuclear Palsy Syndrome |
|
Classic Psp Syndrome
|
Richardson Syndrome
|
|
Steele-Richardson-Olszewski Disease
|
Progressive Supranuclear Palsy
|
|
|
| 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
|
|
|
| Temporal Lobe Neoplasm |
|
Neoplasm Of Temporal Lobe
|
Malignant Neoplasm Of Temporal Lobe
|
|
Tumor Of Temporal Lobe
|
|
|
| Frontotemporal Lobar Degeneration With Tdp43 Inclusions, Grn-Related |
|
Primary Progressive Aphasia
|
Grn-Related Frontotemporal Lobar Degeneration With Tdp43 Inclusions
|
|
Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions
|
Frontotemporal Dementia, Ubiquitin-Positive
|
|
Aphasia, Primary Progressive
|
Ppa
|
|
Ftld-Tdp, Grn-Related
|
Frontotemporal Dementia With Tdp43 Inclusions, Grn-Related
|
|
Ftldu
|
Ftdu
|
|
Dementia, Hereditary Dysphasic Disinhibition
|
Hddd
|
|
Primary Progressive Aphasia Syndrome
|
Mesulam Syndrome
|
|
Ubiquitin-Positive Frontotemporal Dementia
|
UP-FTD
|
|
Tau-Negative Frontotemporal Dementia Linked To Chromosome 17
|
Aphasia Primary Progressive
|
|
Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions, Susceptibility To
|
Aphasia, Primary Progressive, Susceptibility To
|
|
Frontotemporal Dementia
|
|
|
