| Diseases |
Alias |
|
| 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
|
|
|
| Lopes-Maciel-Rodan Syndrome |
|
|
| Juvenile Huntington Disease |
|
Jhd
|
Juvenile Huntington Chorea
|
|
Huntington Disease, Juvenile Onset
|
Juvenile Onset Hd
|
|
|
| Non-Specific Syndromic Intellectual Disability |
|
Complex Neurodevelopmental Disorder
|
|
|
| Dentatorubral-Pallidoluysian Atrophy |
|
DRPLA
|
Naito-Oyanagi Disease
|
|
Haw River Syndrome
|
Myoclonic Epilepsy With Choreoathetosis
|
|
Nod
|
Ataxia, Chorea, Seizures, And Dementia
|
|
Dentatorubropallidoluysian Atrophy
|
Hrs
|
|
Naito Oyanagi Disease
|
Dentatorubral Pallidoluysian Atrophy
|
|
Dentatorubro-Pallidoluysian Atrophy
|
Myoclonic Epilepsies, Progressive
|
|
Atrophy, Pallidoluysian, Dentatorubral
|
|
|
| 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
|
|
|
| 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
|
|
|
| Alexander Disease |
|
Alexander'S Disease
|
ALXDRD
|
|
Alexanders Leukodystrophy
|
Axd
|
|
Demyelinogenic Leukodystrophy
|
Megalencephaly In Infancy Accompanied By Progressive Spasticity And Dementia
|
|
Alx
|
Dysmyelinogenic Leukodystrophy
|
|
Fibrinoid Degeneration Of Astrocytes
|
Leukodystrophy With Rosenthal Fibers
|
|
Alexander Disease Type Ii
|
Axd Type Ii
|
|
Alexander Disease Type I
|
Axd Type I
|
|
Alexanders Disease
|
Alexander'S Leukodystrophy
|
|
|
| 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
|
|
|
| Spinocerebellar Ataxia 1 |
|
Spinocerebellar Ataxia Type 1
|
SCA1
|
|
Olivopontocerebellar Atrophy I
|
Opca1
|
|
Opca4
|
Menzel Type Opca
|
|
Schut-Haymaker Type Opca
|
Spinocerebellar Atrophy I
|
|
Opca I
|
Olivopontocerebellar Atrophy Iv
|
|
Opca Iv
|
Cerebelloparenchymal Disorder I
|
|
Cpd1
|
Olivopontocerebellar Atrophy 1
|
|
Cerebelloparenchymal Disorder 1
|
Olivopontocerebellar Atrophy 4
|
|
Spinocerebellar Atrophy 1
|
Type 1 Spinocerebellar Ataxia
|
|
Spinocerebellar Ataxia-1
|
Ataxia, Spinocerebellar, Type 1
|
|
|
| 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
|
|
|
| Movement Disease |
|
Movement Disorders
|
Movement Disorder
|
|
|
| Choreatic Disease |
|
|
| Autosomal Dominant Cerebellar Ataxia |
|
Spinocerebellar Ataxia
|
Adca
|
|
Pierre Marie Cerebellar Ataxia
|
Ataxia, Spinocerebellar
|
|
Sca
|
Autosomal Dominant Spinocerebellar Ataxia
|
|
Spinocerebellar Ataxias
|
|
|
| Dystonia |
|
Dystonic Disease
|
Dystonic Disorder
|
|
Dystonia Disorders
|
Neuroleptic Dyskinesia
|
|
|
| Open-Angle Glaucoma |
|
Glaucoma Simplex
|
Pigmentary Glaucoma
|
|
Wide-Angle Glaucoma
|
Glaucoma, Open-Angle
|
|
Open Angle Glaucoma
|
Glaucoma Open-Angle
|
|
Chronic Simple Glaucoma
|
Coag - [Chronic Open-Angle Glaucoma]
|
|
Csg - [Chronic Simple Glaucoma]
|
Poag - [Primary Open-Angle Glaucoma]
|
|
Oag - [Open-Angle Glaucoma]
|
Chronic Glaucoma
|
|
Chronic Open Angle Glaucoma
|
Simple Glaucoma
|
|
Chronic Noncongestive Glaucoma
|
Ltg - [Low Tension Glaucoma]
|
|
Noncongestive Glaucoma
|
Nonobstructive Glaucoma
|
|
Normal Pressure Glaucoma
|
Primary Low Tension Glaucoma
|
|
Low-Tension Glaucoma
|
Residual Stage Low Tension Glaucoma
|
|
Open Cleft Glaucoma
|
|
|
| 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
|
|
|
| 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
|
|
|
| Middle Cranial Fossa Meningioma |
|
Meningioma Of The Middle Cranial Fossa
|
|
|
| Muscular Atrophy |
|
Muscle Wasting
|
Amyotrophia
|
|
Wasting - Muscle
|
Skeletal Muscle Atrophy
|
|
|
| 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 |
|
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
|
|
|
| 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
|
|
|
| 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]
|
|
|
| Multiple System Atrophy 1 |
|
Multiple System Atrophy
|
Shy-Drager Syndrome
|
|
Msa
|
MSA1
|
|
Multiple System Atrophy 1, Susceptibility To
|
Sporadic Olivopontocerebellar Atrophy
|
|
Multisystem Atrophy
|
Msa1, Susceptibility To
|
|
Multiple System Atrophy, Susceptibility To
|
Opca
|
|
Progressive Autonomic Failure With Multiple System Atrophy
|
Sds
|
|
|
| Parkinson Disease 23, Autosomal Recessive Early-Onset |
|
Autosomal Recessive Early-Onset Parkinson Disease 23
|
PARK23
|
|
Parkinson Disease 23, Autosomal Recessive, Early Onset
|
Parkinson'S Disease 23
|
|
Autosomal Recessive Early-Onset Parkinson'S Disease 23
|
Parkinson Disease, Type 23, Autosomal Recessive, Early Onset
|
|
|
| Cerebellar Disease |
|
Cerebellar Diseases
|
Cerebellar Dysfunction
|
|
Cerebellar Abnormality
|
Cerebellar Disorders
|
|
|
| Chronic Myelomonocytic Leukemia |
|
Leukemia, Myelomonocytic, Chronic
|
Cmml
|
|
Leukemia Myelomonocytic Chronic
|
Cmml - [Chronic Myelomonocytic Leukaemia]
|
|
Chronic Myelomonocytic Leukaemia Without Mention Of Remission
|
Chronic Monocytic Leukaemia
|
|
Chronic Monocytoid Leukaemia
|
|
|
| Fatal Familial Insomnia |
|
Insomnia, Fatal Familial
|
FFI
|
|
Familial Fatal Insomnia
|
Insomnia Familial Fatal
|
|
Insomnia Fatal Familial
|
Insomnia, Fatal, Familial
|
|
Ffi - [Fatal Familial Insomnia]
|
|
|
| Huntington Disease-Like 2 |
|
HDL2
|
Huntington'S Disease-Like 2
|
|
Huntington Disease-Like, Type 2
|
|
|
| Kuru |
|
Kuru, Susceptibility To
|
Kuru Encephalopathy
|
|
Kuru Encephalitis
|
Kuru Disease
|
|
|
| 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
|
|
|
| Toxic Encephalopathy |
|
Neurotoxicity
|
Neurotoxicity Syndromes
|
|
Neurotoxicity Syndrome
|
Encephalopathy, Toxic
|
|
|
| Hereditary Ataxia |
|
Sca
|
Spinocerebellar Ataxia
|
|
Ataxias Hereditary
|
Ataxias, Hereditary
|
|
|
| Pheochromocytoma |
|
Pheochromocytoma, Susceptibility To
|
Phaeochromocytoma
|
|
Adrenal Gland Chromaffin Paraganglioma
|
Adrenal Gland Chromaffinoma
|
|
Adrenal Gland Paraganglioma
|
Adrenal Gland Pheochromocytoma
|
|
Chromaffin Paraganglioma Of The Adrenal Gland
|
Intraadrenal Paraganglioma
|
|
PCC
|
Chromaffin Cell Tumor
|
|
Medullary Chromaffinoma
|
Medullary Paraganglioma
|
|
Pheochromoblastoma
|
Pheochromocytomas
|
|
Chromaffin Cell Neoplasm
|
Pheochromocytoma, Malignant
|
|
|
| Dialysis-Related Amyloidosis |
|
Abeta2m Amyloidosis
|
Amyloidosis Beta2m
|
|
Beta2-Microglobulinic Amyloidosis
|
Variant Abeta2m Amyloidosis
|
|
Autosomal Dominant Beta2-Microglobulinic Amyloidosis
|
Aβ2m Amyloidosis
|
|
Dialysis-Related Beta2-Microglobulin Amyloidosis
|
Amyloidosis Dialysis-Related
|
|
Beta-2-Microglobulin Amyloidosis
|
Dra
|
|
Hemodialysis-Associated Amyloidosis
|
|
|
| Amyloidosis, Hereditary, Transthyretin-Related |
|
Transthyretin Amyloidosis
|
Familial Amyloid Polyneuropathy
|
|
Ttr Amyloid Neuropathy
|
Transthyretin Amyloid Neuropathy
|
|
Transthyretin Amyloid Polyneuropathy
|
Fap
|
|
Familial Transthyretin Amyloidosis
|
Amyloidosis Transthyretin Related
|
|
Type I Familial Amyloid Polyneuropathy
|
Familial Amyloid Polyneuropathy Type I
|
|
Attrv122i Amyloidosis
|
Hereditary Amyloidosis, Transthyretin-Related
|
|
Amyloid Polyneuropathy, Familial
|
Attr Amyloidosis
|
|
Attrm Amyloidosis
|
Corino De Andrade'S Disease
|
|
Paramyloidosis
|
Transthyretin-Related Hereditary Amyloidosis
|
|
Ttr Amyloidosis
|
Hereditary Attr Amyloidosis
|
|
Portuguese Polyneuritic Amyloidosis
|
Portuguese Type Familial Amyloid Neuropathy
|
|
Swiss Type Amyloid Polyneuropathy
|
Type Ii Familial Amyloid Polyneuropathy
|
|
Attrv30m Amyloidosis
|
Attrv30m-Related Amyloidosis
|
|
Familial Amyloid Polyneuropathy, Portuguese-Swedish-Japanese Type
|
Attr Cardiomyopathy
|
|
Attrv122i-Related Amyloidosis
|
Ttr-Related Amyloid Cardiomyopathy
|
|
Ttr-Related Cardiac Amyloidosis
|
Transthyretin Amyloid Cardiopathy
|
|
Transthyretin-Related Familial Amyloid Cardiomyopathy
|
Amyloidosis, Transthyretin-Related
|
|
AMYL-TTR
|
Amyloidosis I
|
|
Amyloidosis Ohio Type
|
Amyloidosis Type 7
|
|
Amyloidosis Vii
|
Amyloid Polyneuropathy
|
|
Attr
|
Familial Amyloid Polyneuropathy Type Ii
|
|
Hereditary Amyloidosis Transthyretin-Related
|
Leptomeningeal Amyloidosis
|
|
Meningocerebrovascular Amyloidosis
|
Oculoleptomeningeal Amyloidosis
|
|
Familial Amyloid Polyneuropathies
|
Amyloidosis, Leptomeningeal
|
|
Senile Cardiac Amyloidosis
|
Amyloid Neuropathies, Familial
|
|
Danish Type Familial Amyloid Cardiomyopathy
|
Familial Amyloid Neuropathy, Portuguese Type
|
|
Amyloid Polyneuropathy, Swiss Type
|
Hereditary Oculoleptomeningeal Amyloid Angiopathy
|
|
Amyloid Neuropathies
|
|
|
| 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
|
|
|
| Chronic Wasting Disease |
|
|
| Neuroacanthocytosis |
|
Neuroacanthocytosis Syndrome
|
|
|
| Spinocerebellar Ataxia 17 |
|
Spinocerebellar Ataxia Type 17
|
SCA17
|
|
Huntington Disease-Like 4
|
Hdl4
|
|
Olivopontocerebellar Atrophy V
|
Cerebelloparenchymal Disorder Ii
|
|
Opca5
|
Cpd2
|
|
Sca 17
|
Ataxia, Spinocerebellar, Type 17
|
|
|
| Retinitis Pigmentosa-Deafness Syndrome |
|
Retinitis Pigmentosa 8, Formerly
|
Rp8, Formerly
|
|
Retinitis Pigmentosa 21, Formerly
|
Rp21, Formerly
|
|
Usher Syndrome
|
|
|
| Spinocerebellar Ataxia 7 |
|
Spinocerebellar Ataxia Type 7
|
SCA7
|
|
Opca3
|
Opca Iii
|
|
Olivopontocerebellar Atrophy Iii
|
Opca With Retinal Degeneration
|
|
Opca With Macular Degeneration And External Ophthalmoplegia
|
Adca, Type Ii
|
|
Autosomal Dominant Cerebellar Ataxia Type 2
|
Olivopontocerebellar Atrophy 3
|
|
Autosomal Dominant Cerebellar Ataxia, Type Ii
|
Autosomal Dominant Cerebellar Ataxia Type Ii
|
|
Adca2
|
Adcaii
|
|
Ataxia With Pigmentary Retinopathy
|
Cerebellar Syndrome-Pigmentary Maculopathy Syndrome
|
|
Olivopontocerebellar Atrophy With Retinal Degeneration
|
Spinocerebellar Ataxia-7
|
|
Ataxia, Spinocerebellar, Type 7
|
|
|
| Anosognosia |
|
|
| 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
|
|
|
| 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
|
|
|
| Myotonic Disease |
|
Myotonic Disorders
|
Myotonic Syndrome
|
|
Symptomatic Myotonia
|
|
|
| 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]
|
|
|
| Choreoacanthocytosis |
|
Chorea-Acanthocytosis
|
CHAC
|
|
Acanthocytosis With Neurologic Disorder
|
Levine-Critchley Syndrome
|
|
Choreaacanthocytosis
|
Chorea Acanthocytosis
|
|
Neuroacanthocytosis
|
Levine-Critchley Syndrome, Formerly
|
|
Neuroacanthocytosis, Formerly
|
Choreo-Acanthocytosis
|
|
Acanthocytosis Chorea
|
Chorea Acanthocytosis Syndrome
|
|
|
| Intellectual Developmental Disorder, X-Linked, Syndromic, Wilson-Turner Type |
|
Wilson-Turner Syndrome
|
WTS
|
|
Mrxs6
|
X-Linked Intellectual Disability-Gynecomastia-Obesity Syndrome
|
|
Mrxswt
|
Wilson-Turner X-Linked Mental Retardation Syndrome
|
|
Mental Retardation, X-Linked, Syndromic 6
|
Mental Retardation, X-Linked, With Gynecomastia And Obesity
|
|
Intellectual Disability, X-Linked, Syndromic 6
|
Intellectual Disability, X-Linked, With Gynecomastia And Obesity
|
|
Wilson Turner Intellectual Disability Syndrome
|
X-Linked Intellectual Disability - Gynecomastia - Obesity
|
|
|
| Alzheimer Disease 13 |
|
AD13
|
Alzheimer Disease-13
|
|
Alzheimer'S Disease 13
|
Alzheimer'S Disease 13, Late Onset
|
|
|
| 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
|
|
|
| Spinocerebellar Ataxia 8 |
|
Spinocerebellar Ataxia Type 8
|
SCA8
|
|
Ataxia, Spinocerebellar, Type 8
|
|
|
| Fragile X-Associated Tremor/Ataxia Syndrome |
|
Fxtas Syndrome
|
Fragile X Tremor/Ataxia Syndrome
|
|
Fxtas
|
|
|
| Spinal Muscular Atrophy |
|
Sma
|
5q Sma
|
|
Proximal Sma
|
Sma-Associated Sma
|
|
Spinal Amyotrophies
|
Spinal Amyotrophy
|
|
Spinal Muscle Degeneration
|
Spinal Muscle Wasting
|
|
Muscular Atrophy Spinal
|
Atrophy, Muscular, Spinal
|
|
Hereditary Motor Neuronopathy
|
Progressive Muscular Atrophy
|
|
Sma - [Spinal Muscular Atrophy]
|
|
|
| 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
|
|
|
| Neuroblastoma |
|
Nb
|
Neuroblastoma, Susceptibility To
|
|
Neuroblastomas
|
Central Neuroblastoma
|
|
|
| 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
|
|
|
| Autism |
|
Autistic Disorder
|
Autism Susceptibility 1
|
|
Childhood Autism
|
Autistic Disorder Of Childhood Onset
|
|
Infantile Autism
|
Kanner'S Syndrome
|
|
Autistic
|
|
|
| Syndromic X-Linked Intellectual Disability |
|
X-Linked Syndromic Intellectual Disability
|
|
|
| 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
|
|
|
| Syndromic Intellectual Disability |
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| 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
|
|
|
| Peripheral Nervous System Disease |
|
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
| 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
|
|
|
| Myopathy |
|
Muscular Diseases
|
Myopathies
|
|
|
| Congenital Nervous System Abnormality |
|
Congenital Neurologic Anomaly
|
Congenital Nervous System Disorder
|
|
|
| Retinitis Pigmentosa |
|
RP
|
Rod-Cone Dystrophy
|
|
Autosomal Recessive Retinitis Pigmentosa
|
Non-Syndromic Retinitis Pigmentosa
|
|
Pericentral Pigmentary Retinopathy
|
Pigmentary Retinopathy
|
|
Tapetoretinal Degeneration
|
Rcd
|
|
Retinitis Pigmentosa Autosomal Recessive
|
ARRP
|
|
Retinitis Pigmentosa, Autosomal Recessive
|
Retinitis Pigmentosa 1
|
|
|
