| Diseases |
Alias |
|
| Amyotrophic Lateral Sclerosis 15 With Or Without Frontotemporal Dementia |
|
Amyotrophic Lateral Sclerosis 15, With Or Without Frontotemporal Dementia
|
ALS15
|
|
Sclerosis, Lateral, Amyotrophic, Type 15, With/Without Frontotemporal Dementia
|
|
|
| Amyotrophic Lateral Sclerosis Type 15 |
|
Amyotrophic Lateral Sclerosis 15, With Or Without Frontotemporal Dementia
|
Als15
|
|
Amyotrophic Lateral Sclerosis 15
|
|
|
| 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
|
|
|
| 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
|
|
|
| Amyotrophic Lateral Sclerosis 18 |
|
Amyotrophic Lateral Sclerosis Type 18
|
ALS18
|
|
Sclerosis, Lateral, Amyotrophic, Type 18
|
|
|
| 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
|
|
|
| Amyotrophic Lateral Sclerosis 16, Juvenile |
|
Amyotrophic Lateral Sclerosis Type 16
|
ALS16
|
|
Amyotrophic Lateral Sclerosis 16
|
Sclerosis, Lateral, Amyotrophic, Type 16, Juvenile
|
|
|
| Amyotrophic Lateral Sclerosis 19 |
|
Amyotrophic Lateral Sclerosis Type 19
|
ALS19
|
|
Sclerosis, Lateral, Amyotrophic, Type 19
|
|
|
| Amyotrophic Lateral Sclerosis Type 14 |
|
Als14
|
Amyotrophic Lateral Sclerosis 14
|
|
Amyotrophic Lateral Sclerosis, With Or Without Frontotemporal Dementia
|
Amyotrophic Lateral Sclerosis 14 With Or Without Frontotemporal Dementia
|
|
|
| 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
|
|
|
| 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 20 |
|
Amyotrophic Lateral Sclerosis Type 20
|
ALS20
|
|
Sclerosis, Lateral, Amyotrophic, Type 20
|
|
|
| Multisystem Proteinopathy |
|
|
| Amyotrophic Lateral Sclerosis Type 22 |
|
Als 22
|
Amyotrohpic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia
|
|
Amyotrophic Lateral Sclerosis 22
|
|
|
| Brown-Vialetto-Van Laere Syndrome |
|
|
| 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]
|
|
|
| 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
|
|
|
| Amyotrophic Lateral Sclerosis Type 12 |
|
Amyotrophic Lateral Sclerosis 12
|
Als12
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 12
|
|
|
| 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
|
|
|
| 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
|
|
|
| Progressive Bulbar Palsy |
|
Bulbar Palsy, Progressive
|
Progressive Bulbar Atrophy
|
|
Bulbar Palsy
|
Pbp - [Progressive Bulbar Palsy]
|
|
Progressive Bulbar Paralysis
|
Bulbar Paralysis
|
|
Chronic Bulbar Palsy
|
Chronic Bulbar Paralysis
|
|
Supranuclear Bulbar Paralysis
|
|
|
| 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
|
|
|
| Giant Axonal Neuropathy 2 |
|
|
| Perry Syndrome |
|
Parkinsonism With Alveolar Hypoventilation And Mental Depression
|
PERRYS
|
|
|
| Amyotrophic Lateral Sclerosis 8 |
|
Amyotrophic Lateral Sclerosis Type 8
|
ALS8
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 8
|
|
|
| Amyotrophic Lateral Sclerosis 4, Juvenile |
|
Amyotrophic Lateral Sclerosis Type 4
|
ALS4
|
|
Amyotrophic Lateral Sclerosis 4
|
Dhmn With Upper Motor Neuron Signs
|
|
Distal Hereditary Motor Neuropathy With Upper Motor Neuron Signs
|
Neuronopathy, Distal Hereditary Motor, With Pyramidal Features
|
|
Als 4
|
Distal Hereditary Motor Neuropathy With Pyramidal Features
|
|
Amyotrophic Lateral Sclerosis Juvenile 4
|
Neuronopathy Distal Hereditary Motor With Pyramidal Features
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 4
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Autosomal Dominant Cerebellar Ataxia |
|
Spinocerebellar Ataxia
|
Adca
|
|
Pierre Marie Cerebellar Ataxia
|
Ataxia, Spinocerebellar
|
|
Sca
|
Autosomal Dominant Spinocerebellar Ataxia
|
|
Spinocerebellar Ataxias
|
|
|
| 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
|
|
|
| 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
|
|
|
