| Diseases |
Alias |
|
| Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia |
|
Amyotrophic Lateral Sclerosis Type 10
|
ALS10
|
|
Amyotrophic Lateral Sclerosis 10, With Or Without Ftd
|
Frontotemporal Lobar Degeneration, Tardbp-Related
|
|
Amyotrophic Lateral Sclerosis 10
|
Amyotrophic Lateral Sclerosis 10, With Or Without Frontotemporal Dementia
|
|
Tardbp-Related Frontotemporal Lobar Degeneration With Tdp43 Inclusions
|
Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia And With Tdp43 Inclusions
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 10
|
|
|
| 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
|
|
|
| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1 |
|
FTDALS1
|
Frontotemporal Dementia And/Or Motor Neuron Disease
|
|
Ftdmnd
|
Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia
|
|
Alsftd
|
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis
|
|
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-1
|
Frontotemporal Dementia With Motor Neuron Disease
|
|
Ftdals
|
Ftd-Als
|
|
Ftd-Mnd
|
Frontotemporal Dementia With Amyotrophic Lateral Sclerosis
|
|
Amyotrophic Lateral Sclerosis With Frontotemporal Dementia 1
|
Amyotrophic Lateral Sclerosis/Frontotemporal Dementia
|
|
Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis
|
Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia 1
|
|
Frontotemporal Lobar Degeneration
|
Grn-Related Frontotemporal Dementia
|
|
|
| Amyotrophic Lateral Sclerosis 1 |
|
Amyotrophic Lateral Sclerosis
|
ALS
|
|
Lou Gehrig Disease
|
Amyotrophic Lateral Sclerosis Type 1
|
|
Charcot Disease
|
ALS1
|
|
Amyotrophic Lateral Sclerosis, Susceptibility To
|
Fals
|
|
Lou Gehrig'S Disease
|
Mnd
|
|
Motor Neuron Disease
|
Familial Amyotrophic Lateral Sclerosis
|
|
Amyotrophic Lateral Sclerosis 1, Familial
|
Amyotrophic Lateral Sclerosis 1, Autosomal Dominant
|
|
Motor Neuron Disease, Bulbar
|
Motor Neurone Disease
|
|
Amyotrophic Lateral Sclerosis With Dementia
|
Dementia With Amyotrophic Lateral Sclerosis
|
|
Motor Neuron Disease, Amyotrophic Lateral Sclerosis
|
Sclerosis, Lateral, Amyotrophic
|
|
Sclerosis, Lateral, Amyotrophic, Type 1
|
Amyotrophic Sclerosis
|
|
Als - [Amyotrophic Lateral Sclerosis]
|
Wasting Palsy
|
|
Amyotrophic Paralysis
|
Amyotrophy Lateral Sclerosis
|
|
Wasting Paralysis
|
Spinal Progressive Amyotrophy
|
|
Progressive Atrophic Paralysis
|
|
|
| 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
|
|
|
| Aphasia |
|
|
| Lateral Sclerosis |
|
Primary Lateral Sclerosis
|
Adult-Onset Primary Lateral Sclerosis
|
|
Adult-Onset Pls
|
Motor Neuron Disease
|
|
Pls
|
Pls - [Primary Lateral Sclerosis]
|
|
Lateral Spinal Sclerosis
|
Lateral Complete Paralysis
|
|
Lateral Incomplete Paralysis
|
Lateral Paralysis
|
|
|
| Corticobasal Degeneration |
|
|
| 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
|
|
|
| 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
|
|
|
| Perry Syndrome |
|
Parkinsonism With Alveolar Hypoventilation And Mental Depression
|
PERRYS
|
|
|
| Speech And Communication Disorders |
|
Language Disorder
|
Communication Disorder
|
|
Language Disorders
|
Communication Disorders
|
|
Speech Language Disorder
|
Speech-Language Disorder
|
|
Communication Impairment
|
Speech And Language Disorder
|
|
|
| Nominal Aphasia |
|
|
| Spinocerebellar Ataxia 2 |
|
Spinocerebellar Ataxia Type 2
|
SCA2
|
|
Amyotrophic Lateral Sclerosis 13
|
Spinocerebellar Degeneration With Slow Eye Movements
|
|
SDSEM
|
Spinocerebellar Atrophy Ii
|
|
Olivopontocerebellar Atrophy Ii
|
Opca2
|
|
Cerebellar Degeneration With Slow Eye Movements
|
Wadia-Swami Syndrome
|
|
Amyotrophic Lateral Sclerosis Type 13
|
ALS13
|
|
Olivopontocerebellar Atrophy Holguin Type
|
Spinocerebellar Ataxia Cuban Type
|
|
Olivopontocerebellar Atrophy, Holguin Type
|
Spinocerebellar Ataxia, Cuban Type
|
|
Amyotrophic Lateral Sclerosis, Susceptibility To, 13
|
Olivopontocerebellar Atrophy 2
|
|
Sca 2
|
Spinocerebellar Ataxia With Slow Eye Movements
|
|
Spinocerebellar Atrophy 2
|
Wadia Swami Syndrome
|
|
Opca Ii
|
Spinocerebellar Ataxia-2
|
|
Ataxia, Spinocerebellar, Type 2
|
|
|
| Associative Agnosia |
|
|
| 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
|
|
|
| Alzheimer Disease 7 |
|
Ad7
|
Alzheimer'S Disease 7
|
|
Alzheimer Disease, Familial, 7
|
Alzheimer Disease-7
|
|
Alzheimer Disease, Familial 7
|
|
|
| Prosopagnosia |
|
|
| Niemann-Pick Disease |
|
Sphingomyelin/Cholesterol Lipidosis
|
Niemann-Pick Diseases
|
|
Lipoid Histiocytosis
|
Sphingomyelin Lipidosis
|
|
Sphingomyelinase Deficiency Disease
|
Lipid Histiocytosis
|
|
Neuronal Cholesterol Lipidosis
|
Neuronal Lipidosis
|
|
Npd
|
Sphingomyelinase Deficiency
|
|
Niemann-Pick Disease, Type A
|
|
|
| Ideomotor Apraxia |
|
Apraxia, Ideomotor
|
Classic Apraxia
|
|
Ideomotor Dyspraxia
|
Limb-Kinetic Apraxia
|
|
Transcortical Apraxia
|
|
|
| Machado-Joseph Disease |
|
SCA3
|
MJD
|
|
Spinocerebellar Ataxia 3
|
Azorean Disease
|
|
Spinocerebellar Ataxia Type 3
|
Spinocerebellar Atrophy
|
|
Azorean Neurologic Disease
|
Spinopontine Atrophy
|
|
Nigrospinodentatal Degeneration
|
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
|
|
|
| Agraphia |
|
|
| Multisystem Proteinopathy |
|
|
| Arteriolosclerosis |
|
|
| Writing Disorder |
|
|
| Amyotrophic Lateral Sclerosis Type 6 |
|
Amyotrophic Lateral Sclerosis 6, Autosomal Recessive
|
Als6
|
|
Amyotrophic Lateral Sclerosis 6, With Or Without Frontotemporal Dementia
|
Autosomal Recessive Amyotrophic Lateral Sclerosis 6
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 6
|
Amyotrophic Lateral Sclerosis 6
|
|
|
| Amyotrophic Lateral Sclerosis Type 22 |
|
Als 22
|
Amyotrohpic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia
|
|
Amyotrophic Lateral Sclerosis 22
|
|
|
| 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
|
|
|
| Muscular Atrophy |
|
Muscle Wasting
|
Amyotrophia
|
|
Wasting - Muscle
|
Skeletal Muscle Atrophy
|
|
|
| Dysgraphia |
|
|
| Amyotrophic Lateral Sclerosis 8 |
|
Amyotrophic Lateral Sclerosis Type 8
|
ALS8
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 8
|
|
|
| Progressive Muscular Atrophy |
|
Progressive Spinal Muscular Atrophy
|
Pure Progressive Muscular Atrophy
|
|
Pma
|
Hereditary Spinal Muscle Atrophy
|
|
Pma - [Progressive Muscular Atrophy]
|
Progressive Muscle Atrophy
|
|
Progressive Spinal Muscle Atrophy
|
Duchenne-Aran Atrophy
|
|
Duchenne-Aran Muscle Atrophy
|
Hereditary Sma - [Spinal Muscle Atrophy]
|
|
|
| Amyotrophic Lateral Sclerosis 11 |
|
Amyotrophic Lateral Sclerosis Type 11
|
ALS11
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 11
|
|
|
| Parkinsonism |
|
Parkinsonism-Plus
|
Idiopathic Parkinsonism
|
|
Primary Parkinsonism
|
Paralysis Agitans Syndrome
|
|
Parkinsonian Syndrome
|
Trembling Paralysis
|
|
Paralysis Agitans
|
Shaking Palsy
|
|
Shaking Paralysis
|
|
|
| Liposarcoma |
|
|
| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 2 |
|
FTDALS2
|
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-2
|
|
Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis, Type 2
|
|
|
| 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]
|
|
|
| Amyotrophic Lateral Sclerosis 4, Juvenile |
|
Amyotrophic Lateral Sclerosis Type 4
|
ALS4
|
|
Amyotrophic Lateral Sclerosis 4
|
Dhmn With Upper Motor Neuron Signs
|
|
Distal Hereditary Motor Neuropathy With Upper Motor Neuron Signs
|
Neuronopathy, Distal Hereditary Motor, With Pyramidal Features
|
|
Als 4
|
Distal Hereditary Motor Neuropathy With Pyramidal Features
|
|
Amyotrophic Lateral Sclerosis Juvenile 4
|
Neuronopathy Distal Hereditary Motor With Pyramidal Features
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 4
|
|
|
| Postencephalitic Parkinson Disease |
|
Postencephalitic Parkinsonism
|
Parkinson Disease, Postencephalitic
|
|
|
| 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
|
|
|
| Amyotrophic Lateral Sclerosis 19 |
|
Amyotrophic Lateral Sclerosis Type 19
|
ALS19
|
|
Sclerosis, Lateral, Amyotrophic, Type 19
|
|
|
| Huntington Disease |
|
Huntington'S Disease
|
Huntington Chorea
|
|
Huntington'S Chorea
|
HD
|
|
Huntington Chronic Progressive Hereditary Chorea
|
Juvenile Huntington Disease
|
|
Chronic Progressive Chorea
|
Chronic Progressive Hereditary Chorea
|
|
Hc - [Huntington Chorea]
|
Hereditary Chorea
|
|
Progressive Hereditary Chorea
|
|
|
| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 3 |
|
FTDALS3
|
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-3
|
|
Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis, Type 3
|
|
|
| Amyotrophic Lateral Sclerosis, Juvenile, With Dementia |
|
Juvenile Amyotrophic Lateral Sclerosis With Dementia
|
Als-Dementia Complex
|
|
|
| Nonaka Myopathy |
|
Gne Myopathy
|
Hibm
|
|
Distal Myopathy With Rimmed Vacuoles
|
Hereditary Inclusion Body Myopathy
|
|
Ibm2
|
Inclusion Body Myopathy, Quadriceps-Sparing
|
|
Qsm
|
Dmrv
|
|
Distal Myopathy, Nonaka Type
|
Inclusion Body Myopathy 2
|
|
Inclusion Body Myopathy, Autosomal Recessive
|
NM
|
|
Nonaka Distal Myopathy
|
Myopathy, Distal, With Or Without Rimmed Vacuoles
|
|
Inclusion Body Myopathy, Hereditary, Autosomal Recessive
|
Inclusion Body Myopathy Type 2
|
|
Quadriceps-Sparing Myopathy
|
Quadriceps Sparing Myopathy
|
|
Rimmed Vacuole Myopathy
|
Inclusion Body Myopathy 2, Autosomal Recessive, Formerly
|
|
Ibm2, Formerly
|
Hibm2
|
|
Hereditary Inclusion Body Myopathy Type 2
|
Inclusion Body Myopathy 2, Autosomal Recessive
|
|
Myopathy, Distal, With Rimmed Vacuoles
|
Inclusion Body Myopathy Autosomal Recessive
|
|
Myopathy, Inclusion Body, Type 2
|
Myopathy, Nonaka
|
|
|
| Simultanagnosia |
|
|
| Pseudobulbar Palsy |
|
|
| Paget'S Disease Of Bone |
|
Osteitis Deformans
|
Paget Disease Of Bone
|
|
Osseous Paget'S Disease
|
Paget Disease Of Bone, Familial
|
|
Bone Paget Disease
|
Familial Paget'S Disease Of Bone
|
|
Paget'S Bone Disease
|
Familial Paget Disease Of Bone
|
|
Paget Disease, Bone
|
Pdb
|
|
Pagets Bone Disease
|
|
|
| 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
|
|
|
| Neuronopathy, Distal Hereditary Motor, Type Viib |
|
HMN7B
|
Hmn Viib
|
|
Dhmn7b
|
Neuropathy, Distal Hereditary Motor, Type Viib
|
|
Distal Hereditary Motor Neuronopathy Type 7b
|
Distal Hereditary Motor Neuropathy Type Viib
|
|
Neuronopathy, Distal Hereditary Motor, Type 7b
|
Neuropathy, Distal Hereditary Motor, With Vocal Cord Paralysis, Type Viib
|
|
Lower Motor Neuron Disease, Dynactin Type
|
Distal Spinal Muscular Atrophy With Vocal Cord Paralysis Type 7b
|
|
Harper-Young Myopathy
|
Neuronopathy, Distal Hereditary Motor, 7b
|
|
Distal Hereditary Motor Neuropathy With Vocal Cord Paralysis Type Viib
|
Lower Motor Neuron Disease Dynactin Type
|
|
Plmnd
|
Progressive Lower Motor Neuron Disease
|
|
Neuropathy, Motor, Distal, Hereditary, Type Viib
|
|
|
| Supranuclear Palsy, Progressive, 1 |
|
Progressive Supranuclear Palsy
|
Steele-Richardson-Olszewski Syndrome
|
|
Supranuclear Palsy, Progressive
|
Progressive Supranuclear Ophthalmoplegia
|
|
Psp
|
PSNP1
|
|
Familial Progressive Supranuclear Palsy
|
Richardson'S Syndrome
|
|
Psp Syndrome
|
Progressive Supranuclear Palsy 1
|
|
Supranuclear Palsy Progressive
|
Ophthalmoplegia, Supranuclear, Progressive
|
|
Steele-Richardson-Olszewksi Syndrome
|
|
|
| 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
|
|
|
| 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]
|
|
|
| Locked-In Syndrome |
|
Locked In Syndrome
|
Cerebromedullospinal Disconnection
|
|
Locked-In State
|
Quadriplegia
|
|
|
| Fragile X Syndrome |
|
FXS
|
Martin-Bell Syndrome
|
|
Fraxa Syndrome
|
Marker X Syndrome
|
|
X-Linked Mental Retardation And Macroorchidism
|
Fragile X Mental Retardation Syndrome
|
|
Fra Syndrome
|
Mental Retardation, X-Linked, Associated With Marxq28
|
|
X-Linked Intellectual Disability And Macroorchidism
|
Frax Syndrome
|
|
Symptomatic Form Of Fragile X Syndrome In Female Carriers
|
Fragile-X Syndrome
|
|
Fraxe Syndrome
|
|
|
| Gerstmann Syndrome |
|
Aphasia-Angular Gyrus Syndrome
|
Developmental Gerstmann Syndrome
|
|
Gs
|
Gerstmann Badal Syndrome
|
|
Gerstmann Tetrad
|
Gerstmann'S Syndrome
|
|
Developmental Gerstmann'S Syndrome
|
|
|
| Alexia |
|
Dyslexia
|
Dyslexia, Acquired
|
|
Acquired Dyslexia
|
Aphemesthaesia
|
|
|
| Spinal And Bulbar Muscular Atrophy, X-Linked 1 |
|
Kennedy Disease
|
Sbma
|
|
Spinal And Bulbar Muscular Atrophy
|
Kennedy'S Disease
|
|
X-Linked Spinal And Bulbar Muscular Atrophy
|
SMAX1
|
|
Kd
|
Kennedy Spinal And Bulbar Muscular Atrophy
|
|
Spinobulbar Muscular Atrophy
|
Bulbospinal Muscular Atrophy, X-Linked
|
|
Bulbospinal Neuronopathy, X-Linked Recessive
|
Xbsn
|
|
Spinal And Bulbar Muscular Atrophy Of Kennedy
|
Bulbospinal Muscular Atrophy
|
|
X-Linked Bulbospinal Amyotrophy
|
Bulbo-Spinal Atrophy, X-Linked
|
|
Spinal Bulbar Muscular Atrophy
|
X-Linked Bulbo-Spinal Atrophy
|
|
X-Linked Spinal Bulbar Muscular Atrophy
|
X-Linked Bsma
|
|
X-Linked Bulbospinal Muscular Atrophy
|
Spinal And Bulbar Muscular Atrophy X-Linked 1
|
|
Bulbospinal Muscular Atrophy X-Linked
|
Bulbospinal Neuronopathy X-Linked Recessive
|
|
Kennedy Disease)
|
Kennedy Syndrome
|
|
Atrophy, Muscular, Spinal And Bulbar, Kennedy Type
|
Atrophy, Muscular, Spinobulbar
|
|
Bulbospinal Neuronopathy
|
|
|
| Akinetic 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
|
|
|
| Kuru |
|
Kuru, Susceptibility To
|
Kuru Encephalopathy
|
|
Kuru Encephalitis
|
Kuru Disease
|
|
|
| Distal Hereditary Motor Neuronopathy Type 7 |
|
Dhmn7
|
Dhmnvpy
|
|
Distal Spinal Muscular Atrophy With Vocal Cord Paralysis
|
|
|
| Amyotrophic Lateral Sclerosis Type 12 |
|
Amyotrophic Lateral Sclerosis 12
|
Als12
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 12
|
|
|
| Fatal Familial Insomnia |
|
Insomnia, Fatal Familial
|
FFI
|
|
Familial Fatal Insomnia
|
Insomnia Familial Fatal
|
|
Insomnia Fatal Familial
|
Insomnia, Fatal, Familial
|
|
Ffi - [Fatal Familial Insomnia]
|
|
|
| Rett Syndrome |
|
Atypical Rett Syndrome
|
RTT
|
|
Rett Disorder
|
Rts
|
|
Autism, Dementia, Ataxia, And Loss Of Purposeful Hand Use
|
Rett Syndrome, Preserved Speech Variant
|
|
Rett Syndrome, Atypical
|
Rett'S Disorder
|
|
Rett Syndrome Variant
|
Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use Syndrome
|
|
Cerebroatrophic Hyperammonemia
|
Rett Like Syndrome
|
|
Rett'S Syndrome
|
Atypical Rtt
|
|
Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use
|
Rett Syndrome Preserved Speech Variant
|
|
Rett Syndrome Zappella Variant
|
Rett Syndrome, Zappella Variant
|
|
|
| Movement Disease |
|
Movement Disorders
|
Movement Disorder
|
|
|
| Epilepsy, Idiopathic Generalized 2 |
|
EIG2
|
Epilepsy, Idiopathic Generalized, Susceptibility To, 2
|
|
Idiopathic Generalized Epilepsy 2
|
Epilepsy, Idiopathic Generalized Locus On Chromosome 14
|
|
Epilepsy, Idiopathic Generalized, Susceptibility To, Locus On Chromosome 14
|
|
|
| Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone With Or Without Frontotemporal Dementia 2 |
|
Ibmpfd2
|
Msp2
|
|
Multisystem Proteinopathy 2
|
|
|
| Disease Of Mental Health |
|
Mental Health
|
Mental Disorders
|
|
|
| Giant Axonal Neuropathy 2 |
|
|
| 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
|
|
|
| Autosomal Dominant Cerebellar Ataxia |
|
Spinocerebellar Ataxia
|
Adca
|
|
Pierre Marie Cerebellar Ataxia
|
Ataxia, Spinocerebellar
|
|
Sca
|
Autosomal Dominant Spinocerebellar Ataxia
|
|
Spinocerebellar Ataxias
|
|
|
| Speech Disorder |
|
|
| Cerebellar Disease |
|
Cerebellar Diseases
|
Cerebellar Dysfunction
|
|
Cerebellar Abnormality
|
Cerebellar Disorders
|
|
|
| Neuromuscular Disease |
|
Neuromuscular Diseases
|
Neuromuscular Disorders
|
|
Neuromuscular Disorder
|
|
|
| Hereditary Spastic Paraplegia |
|
Familial Spastic Paraplegia
|
Hereditary Spastic Paraparesis
|
|
Strumpell-Lorrain Disease
|
Familial Spastic Paraparesis
|
|
Hsp
|
Spg
|
|
Strümpell-Lorrain Disease
|
Spastic Paraplegia, Hereditary
|
|
French Settlement Disease
|
Strumpell-Lorrain Syndrome
|
|
Fsp
|
Spastic Paraplegia, Familial
|
|
Spastic Paraplegia Hereditary
|
Spastic Paraplegia 3, Autosomal Dominant
|
|
Spastic Paraparesis
|
Hereditary Spastic Paralysis
|
|
Familial Spastic Paralysis
|
Hereditary Spastic Ataxia
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| Charcot-Marie-Tooth Disease |
|
Cmt
|
Hmsn
|
|
Hereditary Motor And Sensory Neuropathy
|
Pma
|
|
Cmt - Charcot-Marie-Tooth Disease
|
Charcot Marie Tooth Disease
|
|
Charcot-Marie-Tooth Hereditary Neuropathy
|
Charcot-Marie-Tooth Syndrome
|
|
Peroneal Muscular Atrophy
|
Hereditary Motor And Sensory Neuropathies
|
|
|
