| Diseases |
Alias |
|
| 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
|
|
|
| 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
|
|
|
| Alzheimer Disease 3 |
|
AD3
|
Alzheimer Disease, Type 3
|
|
Alzheimer Disease, Type 3, With Spastic Paraparesis And Apraxia
|
Alzheimer Disease, Type 3, With Spastic Paraparesis And Unusual Plaques
|
|
Alzheimer'S Disease 3
|
Alzheimer Disease, Familial, 3, With Spastic Paraparesis And Apraxia
|
|
Alzheimer Disease 3, Early-Onset
|
Alzheimer Disease, Familial, 3
|
|
Alzheimer Disease, Protection Against, Due To Apoe3-Christchurch
|
Alzheimer Disease 3, Early Onset
|
|
Alzheimer Disease Familial 3
|
Early-Onset Familial Alzheimer Disease 3
|
|
Familial Alzheimer Disease 3
|
Familial Alzheimer Disease 3 With Spastic Paraparesis And Apraxia
|
|
Familial Alzheimer Disease 3 With Spastic Paraparesis And Unusual Plaques
|
Alzheimer Disease, Familial, 3, With Spastic Paraparesis And Unusual Plaques
|
|
Alzheimer Disease, Familial, Type 3
|
|
|
| Cardiomyopathy, Dilated, 1u |
|
CMD1U
|
Dilated Cardiomyopathy 1u
|
|
Cardiomyopathy, Dilated 1u
|
|
|
| Acne Inversa, Familial, 3 |
|
ACNINV3
|
Acne Inversa Familial
|
|
Hidradenitis Suppurativa Familial
|
Acne Inversa, Familial, Type 3
|
|
|
| Early-Onset, Autosomal Dominant Alzheimer Disease |
|
Familial Alzheimer Disease
|
Early-Onset Autosomal Dominant Alzheimer Disease
|
|
Eofad
|
Early-Onset Familial Autosomal Dominant Alzheimer Disease
|
|
Alzheimer'S Disease, Familial
|
|
|
| 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
|
|
|
| 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
|
|
|
| Alzheimer Disease 4 |
|
AD4
|
Alzheimer Disease-4
|
|
Alzheimer'S Disease 4
|
Alzheimer Disease, Familial, 4
|
|
Alzheimer Disease, Familial4
|
Alzheimer'S Disease 4, Early Onset
|
|
Alzheimer Disease, Type 4
|
|
|
| Spastic Paraparesis |
|
|
| 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
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| Congenital Nervous System Abnormality |
|
Congenital Neurologic Anomaly
|
Congenital Nervous System Disorder
|
|
|
| Familial Isolated Dilated Cardiomyopathy |
|
Familial Or Idiopathic Dilated Cardiomyopathy
|
|
|
| Dilated Cardiomyopathy |
|
Familial Dilated Cardiomyopathy
|
Primary Dilated Cardiomyopathy
|
|
Idiopathic Dilated Cardiomyopathy
|
Congestive Cardiomyopathy
|
|
Idiopathic Dilation Cardiomyopathy
|
Primary Familial Dilated Cardiomyopathy
|
|
Cardiomyopathy, Dilated
|
DCM
|
|
Cardiomyopathy, Familial Dilated
|
Dilated Cardiomyopathy, Familial
|
|
Hypokinetic Dilated Cardiomyopathy, Familial
|
Familial Idiopathic Cardiomyopathy
|
|
Fdc
|
Cardiomyopathy, Familial Idiopathic
|
|
Idiopathic Cardiomegaly
|
Dilated Congestive Cardiomyopathy
|
|
Chronic Dilated Cardiomyopathy
|
Ccm - [Congestive Cardiomyopathy]
|
|
Cocm - [Congestive Cardiomyopathy]
|
Dcm - [Dilated Cardiomyopathy]
|
|
Dilated-Hypokinetic Cardiomyopathy
|
Congestive Idiopathic Cardiomyopathy
|
|
Primary Idiopathic Dilated Cardiomyopathy
|
|
|
| Aphasia |
|
|
| Acne |
|
Acne Vulgaris
|
Acne Varioliformis
|
|
Frontalis Acne
|
|
|
| Cerebral Amyloid Angiopathy, Cst3-Related |
|
Cerebral Amyloid Angiopathy
|
Hereditary Cerebral Hemorrhage With Amyloidosis
|
|
Hchwa
|
Hereditary Cystatin C Amyloid Angiopathy
|
|
Cerebral Amyloid Angiopathy, Familial
|
Amyloidosis, Cerebroarterial, Icelandic Type
|
|
Amyloidosis Vi
|
Cerebral Hemorrhage, Hereditary, With Amyloidosis
|
|
Cst3-Related Cerebral Amyloid Angiopathy
|
Cerebral Hemorrhage, Hereditary, With Amyloidosis, Icelandic Variant
|
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Icelandic Variant
|
Caa, Familial
|
|
Cerebral Amyloid Angiopathy, Genetic
|
Acys Amyloidosis
|
|
Cst3-Related Amyloidosis
|
Cystatin Amyloidosis
|
|
Hchwa, Icelandic Type
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Icelandic Type
|
|
Amyloidosis 6
|
AMYL6
|
|
Acys
|
Caa
|
|
Cerebral Amyloid Angiopathy Cst3-Related
|
Cerebroarterial Amyloidosis Icelandic Type
|
|
Cystatin C Amyloidosis
|
Hccaa
|
|
Hchwai
|
Hchwa-I
|
|
Hereditary Cerebral Hemorrhage With Amyloidosis Icelandic Type
|
Cerebral Amyloid Angiopathy Familial
|
|
Angiopathy, Amyloid, Cerebral, Cst3-Related
|
Hereditary Cerebral Amyloid Angiopathy, Icelandic Type
|
|
Familial Cerebral Amyloid Angiopathy
|
Cerebral Amyloid Angiopathy, Hereditary
|
|
|
| Apraxia |
|
|
| Amyloidosis |
|
Amyloid Disease
|
Amyloid
|
|
Amyloid Degeneration
|
Amyloidosis Nos
|
|
Amyloid Deposition
|
Amyloid Infiltration
|
|
Idiopathic Amyloidosis
|
Hyaloid Degeneration
|
|
Lardaceous Degeneration
|
|
|
| Vascular Dementia |
|
Dementia, Vascular
|
Multi Infarct Dementia
|
|
Multifocal Dementia
|
Dementia Vascular
|
|
Vascular Dementia, Susceptibility To
|
Dementia, Multi-Infarct
|
|
Multi-Infarct Dementia
|
|
|
| Visual Agnosia |
|
|
| 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
|
|
|
| Hidradenitis Suppurativa |
|
Acne Inversa
|
Suppurative Hidradenitis
|
|
Acne Inversa, Familial
|
Apocrinitis
|
|
Hidradenitides, Suppurative
|
Hidradenitis, Suppurative
|
|
Suppurative Hidradenitides
|
Inverse Acne
|
|
|
| Inclusion Body Myositis |
|
Ibm
|
Sporadic Inclusion Body Myositis
|
|
Inflammatory Myopathy
|
Myositis, Inclusion Body
|
|
Inflammatory Myopathies
|
Sibm
|
|
Myositis Inclusion Body
|
Nonaka Myopathy
|
|
Inclusion Body Myopathy, Autosomal Recessive
|
Inclusion Body Myopathy, Autosomal Dominant
|
|
Myositis
|
Inclusion Body Myopathy, Sporadic
|
|
|
| Hidradenitis |
|
|
| Cerebral Amyloid Angiopathy, App-Related |
|
Hchwad
|
Amyloidosis, Cerebroarterial, App-Related
|
|
Amyloidosis, Hereditary, With Cerebral Hemorrhage, Dutch Variant
|
Cerebral Amyloid Angiopathy, App-Related, Dutch Variant
|
|
Cerebral Amyloid Angiopathy, App-Related, Iowa Variant
|
Cerebral Amyloid Angiopathy, App-Related, Italian Variant
|
|
Cerebral Amyloid Angiopathy, App-Related, Flemish Variant
|
Cerebral Amyloid Angiopathy, App-Related, Arctic Variant
|
|
Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants
|
App-Related Cerebral Amyloid Angiopathy
|
|
Abetaa21g Amyloidosis
|
Abeta Amyloidosis, Italian Type
|
|
Abeta Amyloidosis, Arctic Type
|
Abeta Amyloidosis, Iowa Type
|
|
Abeta Amyloidosis, Dutch Type
|
Hchwa-D
|
|
Abeta Amyloidosis, Flemish Type
|
Abetaa21g-Related Amyloidosis
|
|
Hchwa, Flemish Type
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Flemish Type
|
|
Abetae22k Amyloidosis
|
Hchwa, Italian Type
|
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Italian Type
|
Abetae22g Amyloidosis
|
|
Hchwa, Arctic Type
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Arctic Type
|
|
Abetad23n Amyloidosis
|
Hchwa, Iowa Type
|
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Iowa Type
|
Abetal34v Amyloidosis
|
|
Abeta Amyloidosis, Piedmont Type
|
Abetal34v-Related Amyloidosis
|
|
Hchwa, Piedmont Type
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Piedmont Type
|
|
Abetae22q Amyloidosis
|
Hchwa, Dutch Type
|
|
Hereditary Cerebral Hemorrhage With Amyloidosis, Dutch Type
|
CAA-APP
|
|
Amyloidosis Cerebroarterial App-Related
|
Amyloidosis Hereditary With Cerebral Hemorrhage Dutch Variant
|
|
Cerebral Amyloid Angiopathy App-Related Arctic Variant
|
Cerebral Amyloid Angiopathy App-Related Dutch Variant
|
|
Cerebral Amyloid Angiopathy App-Related Flemish Variant
|
Cerebral Amyloid Angiopathy App-Related Iowa Variant
|
|
Cerebral Amyloid Angiopathy App-Related Italian Variant
|
Familial Occipital Calcifications With Hemorrhagic Strokes Leukoencephalopathy Arterial Dysplasia Dementia
|
|
Fochs-Ladd
|
Hereditary Cerebral Amyloid Angiopathy Dutch Type
|
|
Hereditary Cerebral Hemorrhage With Amyloidosis Dutch Type
|
Hereditary Cerebral Hemorrhage With Amyloidosis Italian Type
|
|
Cerebral Hemorrhage With Amyloidosis, Hereditary, Dutch Type
|
|
|
| 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
|
|
|
| Mild Cognitive Impairment |
|
|
| Speech And Communication Disorders |
|
Language Disorder
|
Communication Disorder
|
|
Language Disorders
|
Communication Disorders
|
|
Speech Language Disorder
|
Speech-Language Disorder
|
|
Communication Impairment
|
Speech And Language Disorder
|
|
|
| Parkinsonism |
|
Parkinsonism-Plus
|
Idiopathic Parkinsonism
|
|
Primary Parkinsonism
|
Paralysis Agitans Syndrome
|
|
Parkinsonian Syndrome
|
Trembling Paralysis
|
|
Paralysis Agitans
|
Shaking Palsy
|
|
Shaking Paralysis
|
|
|
| Subjective Cognitive Decline |
|
|
| Simultanagnosia |
|
|
| Gerstmann Syndrome |
|
Aphasia-Angular Gyrus Syndrome
|
Developmental Gerstmann Syndrome
|
|
Gs
|
Gerstmann Badal Syndrome
|
|
Gerstmann Tetrad
|
Gerstmann'S Syndrome
|
|
Developmental Gerstmann'S Syndrome
|
|
|
| Anosognosia |
|
|
| Ideomotor Apraxia |
|
Apraxia, Ideomotor
|
Classic Apraxia
|
|
Ideomotor Dyspraxia
|
Limb-Kinetic Apraxia
|
|
Transcortical Apraxia
|
|
|
| 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
|
|
|
| Chromosomal Duplication Syndrome |
|
|
| Nominal Aphasia |
|
|
| Cerebral Amyloid Angiopathy, Itm2b-Related, 1 |
|
Dementia, Familial British
|
Fbd
|
|
Presenile Dementia With Spastic Ataxia
|
Familial British Dementia
|
|
Abri Amyloidosis
|
Cerebral Amyloid Angiopathy, British Type
|
|
Itm2b-Related Cerebral Amyloid Angiopathy 1
|
Familial Dementia, British Type
|
|
Cerebral Amyloid Angiopathy, Itm2b-Related 1
|
CAA-ITM2B1
|
|
Cerebral Amyloid Angiopathy British Type
|
Dementia, Familial, British
|
|
|
| Alexia |
|
Dyslexia
|
Dyslexia, Acquired
|
|
Acquired Dyslexia
|
Aphemesthaesia
|
|
|
| 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
|
|
|
| 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]
|
|
|
| Polycystic Lipomembranous Osteodysplasia With Sclerosing Leukoencephalopathy 1 |
|
Nasu-Hakola Disease
|
Polycystic Lipomembranous Osteodysplasia With Sclerosing Leukoencephalopathy
|
|
Plosl
|
Nhd
|
|
Presenile Dementia With Bone Cysts
|
Plo-Sl
|
|
PLOSL1
|
Dementia, Prefrontal, With Bone Cysts
|
|
Dementia, Progressive, With Lipomembranous Polycystic Osteodysplasia
|
Brain-Bone-Fat Disease
|
|
Progressive Dementia With Lipomembranous Polycystic Osteodysplasia
|
Brain-Bone-Fat Disease
|
|
|
| Fatal Familial Insomnia |
|
Insomnia, Fatal Familial
|
FFI
|
|
Familial Fatal Insomnia
|
Insomnia Familial Fatal
|
|
Insomnia Fatal Familial
|
Insomnia, Fatal, Familial
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Ffi - [Fatal Familial Insomnia]
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| Dyscalculia |
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Disorder Of Arithmetical Skills
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Mathematics Disorder
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Developmental Arithmetic Disorder
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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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| Toxic Encephalopathy |
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Neurotoxicity
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Neurotoxicity Syndromes
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Neurotoxicity Syndrome
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Encephalopathy, Toxic
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| Parkinson Disease, Late-Onset |
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Parkinson Disease
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Parkinson'S Disease
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PD
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PARK
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Parkinson Disease, Susceptibility To
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Late Onset Parkinson'S Disease
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Late Onset Parkinson Disease
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Paralysis Agitans
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Primary Parkinsonism
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Idiopathic Parkinson Disease
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Parkinson'S
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Parkinson Disease, Late-Onset, Susceptibility To
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Parkinson Disease, Age Of Onset, Modifier
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Lewy Body Parkinson Disease
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Idiopathic Parkinson'S Disease
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Pd - [Parkinson Disease]
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Parkinson Disease Nos
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Parkinson, Nos
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Primary Parkinson Disease
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| Amnestic Disorder |
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Amnesia
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Amnestic Syndrome
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Korsakoff'S Psychosis Or Syndrome
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Amnesic Syndrome
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Amnestic Disorder In Conditions Classified Elsewhere
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Korsakoff Psychosis Or Syndrome, Nonalcoholic
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Nonalcoholic Organic Amnesic Syndrome
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Organic Amnesic Syndrome
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| Kuru |
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Kuru, Susceptibility To
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Kuru Encephalopathy
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Kuru Encephalitis
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Kuru Disease
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| Narcolepsy |
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Paroxysmal Sleep
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Gelineau Syndrome
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Narcoleptic Syndrome
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Narcolepsy-Cataplexy Syndrome
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Cataplexy And Narcolepsy
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Narcolepsy, Without Cataplexy
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Gelineau'S Syndrome
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Narcolepsy With Or Without Cataplexy
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Narcolepsy Nos
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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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| Supranuclear Palsy, Progressive, 1 |
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Progressive Supranuclear Palsy
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Steele-Richardson-Olszewski Syndrome
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Supranuclear Palsy, Progressive
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Progressive Supranuclear Ophthalmoplegia
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Psp
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PSNP1
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Familial Progressive Supranuclear Palsy
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Richardson'S Syndrome
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Psp Syndrome
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Progressive Supranuclear Palsy 1
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Supranuclear Palsy Progressive
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Ophthalmoplegia, Supranuclear, Progressive
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Steele-Richardson-Olszewksi Syndrome
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| Disease Of Mental Health |
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Mental Health
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Mental Disorders
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| Normal Pressure Hydrocephalus |
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Low Pressure Hydrocephalus
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Hydrocephalus Normal Pressure
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Hydrocephalus, Normal Pressure
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Normal Pressure Hydrocephalus Nos
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Nph - [Normal Pressure Hydrocephalus]
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Normal Pressure Hydrocephaly
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| Chromosomal Disease |
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Chromosomal Disorders
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Congenital Chromosomal Disease
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| Psychotic Disorder |
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Psychotic Disorders
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Mental Or Behavioural Disorder
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Psychotic
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Mental Disorders
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| Communicating Hydrocephalus |
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Acquired Communicating Hydrocephalus
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| Alzheimer Disease 11 |
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Ad11
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Alzheimer'S Disease 11
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Alzheimer Disease, Familial, 11
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Alzheimer Disease-11
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Alzheimer'S Disease 11, Late Onset
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| Neuroblastoma |
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Nb
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Neuroblastoma, Susceptibility To
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Neuroblastomas
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Central Neuroblastoma
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| Dowling-Degos Disease |
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Reticular Pigment Anomaly Of Flexures
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Dark Dot Disease
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Reticulate Acropigmentation Of Kitamura
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Dowling-Degos Kitamura Disease
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Kitamura Reticulate Acropigmentation
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Ddd
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Dowling-Degos-Kitamura Disease
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Reticular Pigmented Anomaly Of Flexures
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| Movement Disease |
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Movement Disorders
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Movement Disorder
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| Alzheimer Disease 9 |
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AD9
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Alzheimer'S Disease 9
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Alzheimer Disease 9, Susceptibility To
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Alzheimer Disease 9, Late-Onset
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Alzheimer'S Disease 9, Late Onset
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{Alzheimer Disease 9, Susceptibility To}
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| Schizophrenia |
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SCZD
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Schizophrenia With Or Without An Affective Disorder
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Schizophrenia 12
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Schizophrenia, Susceptibility To
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Schizophrenia-1
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Dementia Praecox
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Schizophrenia 1
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| Amyotrophic Lateral Sclerosis 1 |
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Amyotrophic Lateral Sclerosis
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ALS
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Lou Gehrig Disease
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Amyotrophic Lateral Sclerosis Type 1
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Charcot Disease
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ALS1
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Amyotrophic Lateral Sclerosis, Susceptibility To
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Fals
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Lou Gehrig'S Disease
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Mnd
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Motor Neuron Disease
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Familial Amyotrophic Lateral Sclerosis
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Amyotrophic Lateral Sclerosis 1, Familial
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Amyotrophic Lateral Sclerosis 1, Autosomal Dominant
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Motor Neuron Disease, Bulbar
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Motor Neurone Disease
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Amyotrophic Lateral Sclerosis With Dementia
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Dementia With Amyotrophic Lateral Sclerosis
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Motor Neuron Disease, Amyotrophic Lateral Sclerosis
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Sclerosis, Lateral, Amyotrophic
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Sclerosis, Lateral, Amyotrophic, Type 1
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Amyotrophic Sclerosis
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Als - [Amyotrophic Lateral Sclerosis]
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Wasting Palsy
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Amyotrophic Paralysis
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Amyotrophy Lateral Sclerosis
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Wasting Paralysis
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Spinal Progressive Amyotrophy
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Progressive Atrophic Paralysis
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| Alzheimer'S Disease 1 |
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Alzheimer Disease Type 1
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Alzheimer'S Disease 1, Early Onset
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| Stroke, Ischemic |
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Cerebral Infarction
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Stroke
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Ischemic Stroke
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Cerebrovascular Accident
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Cerebral Infarction, Susceptibility To
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Stroke, Ischemic, Susceptibility To
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Cerebral Infarct
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Ischemic Stroke, Susceptibility To
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Stroke, Susceptibility To
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Cva - Cerebral Infarction
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ISCHSTR
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Ischemic Cerebrovascular Accident
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| Huntington Disease |
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Huntington'S Disease
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Huntington Chorea
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Huntington'S Chorea
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HD
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Huntington Chronic Progressive Hereditary Chorea
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Juvenile Huntington Disease
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Chronic Progressive Chorea
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Chronic Progressive Hereditary Chorea
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Hc - [Huntington Chorea]
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Hereditary Chorea
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Progressive Hereditary Chorea
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| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1 |
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FTDALS1
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Frontotemporal Dementia And/Or Motor Neuron Disease
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Ftdmnd
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Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia
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Alsftd
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Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis
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Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-1
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Frontotemporal Dementia With Motor Neuron Disease
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Ftdals
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Ftd-Als
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Ftd-Mnd
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Frontotemporal Dementia With Amyotrophic Lateral Sclerosis
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Amyotrophic Lateral Sclerosis With Frontotemporal Dementia 1
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Amyotrophic Lateral Sclerosis/Frontotemporal Dementia
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Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis
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Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia 1
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Frontotemporal Lobar Degeneration
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Grn-Related Frontotemporal Dementia
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| 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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| Neuronal Ceroid Lipofuscinosis |
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Hereditary Ceroid Lipofuscinosis
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Batten Disease
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Ncl
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Neuronal Ceroid-Lipofuscinoses
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Lipofuscinosis, Ceroid, Neuronal
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Juvenile Neuronal Ceroid Lipofuscinosis
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Cerebromacular Dystrophy
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Cerebromacular Degeneration
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Ceroid-Lipofuscinosis
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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
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Pigmentary Retinal Lipoid Neuronal Heredodegeneration
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| Peripheral Nervous System Disease |
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Peripheral Neuropathy
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Peripheral Nerve Disease
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Peripheral Nerve Disorders
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Neuropathy, Peripheral
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Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
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| Hereditary Spastic Paraplegia |
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Familial Spastic Paraplegia
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Hereditary Spastic Paraparesis
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Strumpell-Lorrain Disease
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Familial Spastic Paraparesis
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Hsp
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Spg
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Strümpell-Lorrain Disease
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Spastic Paraplegia, Hereditary
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French Settlement Disease
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Strumpell-Lorrain Syndrome
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Fsp
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Spastic Paraplegia, Familial
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Spastic Paraplegia Hereditary
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Spastic Paraplegia 3, Autosomal Dominant
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Spastic Paraparesis
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Hereditary Spastic Paralysis
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Familial Spastic Paralysis
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Hereditary Spastic Ataxia
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