| 疾病名称 |
别名 |
|
| Parkinson Disease 6, Autosomal Recessive Early-Onset |
|
Autosomal Recessive Early-Onset Parkinson Disease 6
|
Parkinson Disease 6
|
|
PARK6
|
Parkinson Disease 6, Early Onset
|
|
Parkinson'S Disease 6
|
Parkinson Disease 6, Early-Onset
|
|
Autosomal Recessive Early-Onset Parkinson'S Disease 6
|
Early-Onset Parkinson Disease 6
|
|
Autosomal Recessive Early-Onset Parkinson Disease Type 6
|
Parkinson Disease 6 Early-Onset
|
|
Parkinson Disease 6 Late-Onset Susceptibility To
|
Parkinson Disease Autosomal Recessive Early-Onset Digenic Pink1/Dj1
|
|
Parkinsonism Young Adult Onset
|
Parkinson Disease, Autosomal Recessive Early-Onset, Digenic, Pink1/Dj1
|
|
Parkinson Disease, Type 6, Autosomal Recessive, Early-Onset
|
|
|
| Parkinson Disease 2, Autosomal Recessive Juvenile |
|
Young-Onset Parkinson Disease
|
PARK2
|
|
Pdj
|
Autosomal Recessive Juvenile Parkinson Disease 2
|
|
Epdf
|
Parkinson Disease, Juvenile, Type 2
|
|
Parkinson'S Disease 2
|
Autosomal Recessive Juvenile Parkinson Disease
|
|
Early-Onset Parkinson Disease
|
Parkinson Disease 2
|
|
Parkinson Disease, Juvenile, Autosomal Recessive
|
Parkinsonism, Early-Onset, With Diurnal Fluctuation
|
|
Autosomal Recessive Juvenile Parkinson'S Disease 2
|
Jp
|
|
Juvenile Parkinsonism
|
Parkinson Disease Autosomal Recessive, Early Onset
|
|
Parkinsonism, Early Onset, With Diurnal Fluctuation
|
Yopd
|
|
Autosomal Recessive Early-Onset Parkinson Disease Type 2
|
Chromosome 6-Linked Autosomal Recessive Parkinsonism
|
|
Early-Onset Parkinsonism With Diurnal Fluctuation
|
Parkinsonism Young Adult Onset
|
|
Parkinson Disease, Type 2
|
Parkinsonism, Juvenile
|
|
|
| Parkinsonism |
|
Parkinsonism-Plus
|
Idiopathic Parkinsonism
|
|
Primary Parkinsonism
|
Paralysis Agitans Syndrome
|
|
Parkinsonian Syndrome
|
Trembling Paralysis
|
|
Paralysis Agitans
|
Shaking Palsy
|
|
Shaking Paralysis
|
|
|
| Movement Disease |
|
Movement Disorders
|
Movement Disorder
|
|
|
| Early-Onset Parkinson'S Disease |
|
Early-Onset Parkinson Disease
|
|
|
| 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
|
|
|
| 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
|
|
|
| Kufor-Rakeb Syndrome |
|
Park9
|
Krppd
|
|
KRS
|
Pallidopyramidal Degeneration With Supranuclear Upgaze Paresis And Dementia
|
|
Autosomal Recessive Parkinson Disease 9
|
Parkinson Disease 9
|
|
Parkinson Disease 9, Autosomal Recessive, Juvenile-Onset
|
Autosomal Recessive Juvenile Onset Parkinson Disease 9
|
|
Parkinson Disease Type 9
|
Pallidopyramidal Degeneration With Supranuclear Upgaze Paresis, And Dementia
|
|
Park 9
|
Atp13a2-Related Juvenile Neuronal Ceroid Lipofuscinosis
|
|
Cln12 Disease
|
Juvenile Parkinsonism-Neuronal Ceroid Lipofuscinosis
|
|
Parkinson Disease Autosomal Recessive 9
|
|
|
| Parkinson Disease 15, Autosomal Recessive Early-Onset |
|
Parkinsonian-Pyramidal Syndrome
|
Pallidopyramidal Syndrome
|
|
Parkinson Disease 15, Autosomal Recessive
|
PARK15
|
|
Pkps
|
Pallido-Pyramidal Syndrome
|
|
Parkinson'S Disease 15
|
Autosomal Recessive Early-Onset Parkinson Disease 15
|
|
Autosomal Recessive Early-Onset Parkinson'S Disease 15
|
Pallido-Pyramidal Disease
|
|
Parkinson Disease 15
|
Parkinson Disease 15 Autosomal Recessive
|
|
Pps
|
Parkinson Disease, Type 15
|
|
|
| Dystonia 12 |
|
DYT12
|
Rdp
|
|
Generalized Dystonia
|
Dystonia-12
|
|
Rapid-Onset Dystonia-Parkinsonism
|
Familial Dystonia
|
|
Dystonia Musculorum Deformans
|
Dystonic Disorders
|
|
Idiopathic Familial Dystonia
|
Dystonia-Parkinsonism, Rapid-Onset
|
|
Fragments Of Torsion Dystonia
|
Dyt-Atp1a3
|
|
Rapid-Onset Dystonia Parkinsonism
|
Rodp
|
|
Dystonia, Type 12
|
Dystonia 3, Torsion, X-Linked
|
|
Idiopathic Non-Familial Dystonia
|
Symptomatic Torsion Dystonia
|
|
Dystonia Disorders
|
|
|
| Postencephalitic Parkinson Disease |
|
Postencephalitic Parkinsonism
|
Parkinson Disease, Postencephalitic
|
|
|
| Gaucher Disease, Type I |
|
Glucocerebrosidase Deficiency
|
Acid Beta-Glucosidase Deficiency
|
|
Gba Deficiency
|
GD1
|
|
Gd I
|
Gaucher Disease, Noncerebral Juvenile
|
|
Gaucher Disease Type 1
|
Gaucher Disease Type I
|
|
Gaucher'S Disease Type I
|
Gaucher Disease
|
|
Gd 1
|
Non-Cerebral Juvenile Gaucher Disease
|
|
GD
|
Gaucher Disease 1
|
|
Adult Non-Neuronopathic Gaucher Disease
|
Noncerebral Juvenile Gaucher Disease
|
|
Type 1 Gaucher Disease
|
Gaucher Disease, Type 1
|
|
|
| Muscular Dystrophy, Congenital, Megaconial Type |
|
Megaconial Type Congenital Muscular Dystrophy
|
Congenital Megaconial Myopathy
|
|
Congenital Muscular Dystrophy Due To Phosphatidylcholine Biosynthesis Defect
|
Congenital Muscular Dystrophy With Mitochondrial Structural Abnormalities
|
|
Megaconial Congenital Muscular Dystrophy
|
MDCMC
|
|
Muscular Dystrophy, Congenital, With Mitochondrial Structural Abnormalities
|
Megaconial Congénital Muscular Dystrophy
|
|
Dystrophy, Muscular, Congenital, Megaconial Type
|
|
|
| Rem Sleep Behavior Disorder |
|
Rapid Eye Movement Sleep Behavior Disorder
|
Rem Sleep Behaviour Disorder
|
|
Rapid Eye Movement Sleep Behaviour Disorder
|
Rem - [Rapid Eye Movement] Behaviour Disorder
|
|
|
| Vascular Parkinsonism |
|
|
| Dystonia |
|
Dystonic Disease
|
Dystonic Disorder
|
|
Dystonia Disorders
|
Neuroleptic Dyskinesia
|
|
|
| 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]
|
|
|
| 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
|
|
|
| Gaucher'S Disease |
|
Gaucher Disease
|
Kerasin Thesaurismosis
|
|
Glucocerebrosidase Deficiency
|
Glucosylceramidase Deficiency
|
|
Cerebroside Lipidosis Syndrome
|
Acid Beta-Glucosidase Deficiency
|
|
Glucosylceramide Beta-Glucosidase Deficiency
|
Acute Cerebral Gaucher Disease
|
|
Gaucher Splenomegaly
|
Glucocerebrosidosis
|
|
Glucosyl Cerebroside Lipidosis
|
Kerasin Lipoidosis
|
|
Lipoid Histiocytosis
|
Glocucerebrosidase Deficiency
|
|
Sphingolipidosis 1
|
Gaucher Syndrome
|
|
Gauchers Disease
|
Gd
|
|
Glucosylceramide Lipidosis
|
Kerasin Histiocytosis
|
|
Gaucher Disease, Type 1
|
Gaucher Disease, Type 2
|
|
|
| Sphingolipidosis |
|
|
| Toxic Encephalopathy |
|
Neurotoxicity
|
Neurotoxicity Syndromes
|
|
Neurotoxicity Syndrome
|
Encephalopathy, Toxic
|
|
|
| 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
|
|
|
| Male Infertility |
|
Infertility, Male
|
Infertility Male
|
|
Male Sterility
|
Absolute Infertility
|
|
|
| Optic Nerve Disease |
|
Optic Neuropathy
|
Disorder Of The Second Nerve
|
|
Optic Nerve Disorder
|
Optic Nerve
|
|
Abnormality Of The Optic Nerve
|
Optic Nerve Disorders
|
|
Neuropathy, Optic
|
Disorder Of The Optic Nerve
|
|
|
| Neurodegeneration With Brain Iron Accumulation |
|
Nbia
|
Neurodegeneration With Brain Iron Accumulation Disorders
|
|
Neurodegeneration, With Brain Iron Accumulation
|
|
|
| Mitochondrial Complex I Deficiency, Nuclear Type 1 |
|
Mitochondrial Complex I Deficiency
|
Nadh:Q(1) Oxidoreductase Deficiency
|
|
MC1DN1
|
Nadh-Coenzyme Q Reductase Deficiency
|
|
Isolated Mitochondrial Respiratory Chain Complex I Deficiency
|
Isolated Nadh-Coenzyme Q Reductase Deficiency
|
|
Isolated Nadh-Coq Reductase Deficiency
|
Isolated Nadh-Ubiquinone Reductase Deficiency
|
|
Mitochondrial Nadh Dehydrogenase Component Of Complex I, Deficiency Of
|
Nuclear Type Mitochondrial Complex I Deficiency 1
|
|
Isolated Complex I Deficiency
|
Complex 1 Mitochondrial Respiratory Chain Deficiency
|
|
Nadh Coenzyme Q Reductase Deficiency
|
Complex I Mitochondrial Respiratory Chain Deficiency
|
|
Deficiency Of Mitochondrial Nadh Dehydrogenase Component Of Complex I
|
Nadh:Ubiquinone Oxidoreductase Deficiency
|
|
Complex I, Mitochondrial Respiratory Chain, Deficiency Of
|
|
|
| Leber Hereditary Optic Neuropathy, Modifier Of |
|
Leber Optic Atrophy
|
Leber Hereditary Optic Neuropathy
|
|
LHON
|
Leber'S Hereditary Optic Neuropathy
|
|
Leber Optic Atrophy, Susceptibility To
|
Leber'S Optic Atrophy
|
|
LOAM
|
Loas
|
|
Leber'S Disease
|
Leber'S Optic Neuropathy
|
|
Optic Atrophy, Hereditary, Leber
|
Lhon, Modifier Of
|
|
Optic Atrophy, Leber Type
|
Hereditary Optic Neuroretinopathy
|
|
Leber Hereditary Optic Atrophy
|
Loa
|
|
Optic Atrophy Leber Type
|
Leber Hereditary Optic Neuropathy, Modifier
|
|
Leber Hereditary Optic Neuropathy Susceptibility
|
Modifier Of Leber Hereditary Optic Neuropathy
|
|
Lebers Hereditary Optic Neuropathy
|
Leber Congenital Amaurosis
|
|
|
| Choreatic 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
|
|
|
| Cerebellar Disease |
|
Cerebellar Diseases
|
Cerebellar Dysfunction
|
|
Cerebellar Abnormality
|
Cerebellar Disorders
|
|
|
| Autosomal Dominant Cerebellar Ataxia |
|
Spinocerebellar Ataxia
|
Adca
|
|
Pierre Marie Cerebellar Ataxia
|
Ataxia, Spinocerebellar
|
|
Sca
|
Autosomal Dominant Spinocerebellar Ataxia
|
|
Spinocerebellar Ataxias
|
|
|
| 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
|
|
|
| Mitochondrial Myopathy |
|
Mitochondrial Myopathies
|
Mitochondrial Cytopathy
|
|
Myopathies In Mitochondrial Disorders
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| Peripheral Nervous System Disease |
|
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
| 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
|
|
|
| Leigh Syndrome |
|
Leigh Disease
|
Infantile Subacute Necrotizing Encephalopathy
|
|
Leigh Syndrome Due To Mitochondrial Complex Iv Deficiency
|
LS
|
|
Sne
|
Leigh'S Disease
|
|
Leigh Syndrome Due To Mitochondrial Complex I Deficiency
|
Necrotizing Encephalopathy, Infantile Subacute, Of Leigh
|
|
Subacute Necrotizing Encephalomyelopathy
|
Necrotizing Encephalopathy Infantile Subacute Of Leigh
|
|
Leigh Syndrome Due To Mitochondrial Complex Iii Deficiency
|
Infantile Necrotizing Encephalomyelopathy
|
|
Juvenile Subacute Necrotizing Encephalomyelopathy
|
Leigh'S Necrotizing Encephalopathy
|
|
Subacute Necrotizing Encephalopathy
|
Juvenile Subacute Necrotizing Encephalopathy
|
|
Leigh Syndrome Due To Mitochondrial Complex Ii Deficiency
|
Leigh Syndrome Due To Mitochondrial Complex V Deficiency
|
|
Encephalopathy, Subacute Necrotizing, Infantile
|
Encephalopathy, Subacute Necrotizing, Juvenile
|
|
Maternally Inherited Leigh Syndrome
|
Subacute Necrotising Encephalomyelopathy
|
|
Subacute Necrotising Encephalopathy
|
|
|
| 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
|
|
|
| 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
|
|
|
