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125370
DRPLA
DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY
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Neoplasms
Neoplasms by Histologic Type
Neoplasms, Germ Cell and Embryonal
Neuroectodermal Tumors
Neoplasms, Neuroepithelial
Neuroectodermal Tumors, Primitive
Neuroectodermal Tumors, Primitive, Peripheral
Neuroblastoma
Neoplasms, Glandular and Epithelial
Neoplasms, Neuroepithelial
Neuroectodermal Tumors, Primitive
Neuroectodermal Tumors, Primitive, Peripheral
Neuroblastoma
Neoplasms, Nerve Tissue
Neuroectodermal Tumors
Neoplasms, Neuroepithelial
Neuroectodermal Tumors, Primitive
Neuroectodermal Tumors, Primitive, Peripheral
Neuroblastoma
Musculoskeletal Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Myotonic Dystrophy
Myotonic Disorders
Myotonic Dystrophy
Nervous System Diseases
Autonomic Nervous System Diseases
Primary Dysautonomias
Multiple System Atrophy
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Huntington Disease
Multiple System Atrophy
Olivopontocerebellar Atrophies
Parkinsonian Disorders
Parkinson Disease
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Ataxias
Machado-Joseph Disease
Spinocerebellar Degenerations
Myoclonic Cerebellar Dyssynergia
Olivopontocerebellar Atrophies
Spinocerebellar Ataxias
Machado-Joseph Disease
Dementia
Alzheimer Disease
Huntington Disease
Epilepsy
Epilepsies, Myoclonic
Myoclonic Epilepsies, Progressive
Epilepsies, Partial
Epilepsy, Generalized
Epilepsy, Tonic-Clonic
Status Epilepticus
Hydrocephalus
Hydrocephalus, Normal Pressure
Movement Disorders
Dyskinesias
Chorea
Huntington Disease
Dystonic Disorders
Torticollis
Multiple System Atrophy
Olivopontocerebellar Atrophies
Parkinsonian Disorders
Parkinson Disease
Ocular Motility Disorders
Spinal Cord Diseases
Muscular Atrophy, Spinal
Spinocerebellar Degenerations
Myoclonic Cerebellar Dyssynergia
Olivopontocerebellar Atrophies
Spinocerebellar Ataxias
Machado-Joseph Disease
Cranial Nerve Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Demyelinating Diseases
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Huntington Disease
Myotonic Dystrophy
Spinocerebellar Degenerations
Myoclonic Cerebellar Dyssynergia
Olivopontocerebellar Atrophies
Spinocerebellar Ataxias
Machado-Joseph Disease
Motor Neuron Disease
Muscular Atrophy, Spinal
Multiple System Atrophy
Olivopontocerebellar Atrophies
Olivopontocerebellar Atrophies
Parkinson Disease
Tauopathies
Alzheimer Disease
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Spinocerebellar Ataxias
Machado-Joseph Disease
Athetosis
Chorea
Dystonia
Torticollis
Myoclonus
Tremor
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Intellectual Disability
Mental Retardation, X-Linked
Fragile X Syndrome
Perceptual Disorders
Hallucinations
Psychomotor Disorders
Neuromuscular Manifestations
Muscular Atrophy
Paralysis
Paraplegia
Reflex, Abnormal
Neuromuscular Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Muscular Atrophy, Spinal
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Myotonic Dystrophy
Myotonic Disorders
Myotonic Dystrophy
Muscular Disorders, Atrophic
Eye Diseases
Corneal Diseases
Eye Diseases, Hereditary
Retinitis Pigmentosa
Ocular Motility Disorders
Nystagmus, Pathologic
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Male Urogenital Diseases
Genital Diseases, Male
Infertility
Infertility, Male
Oligospermia
Urologic Diseases
Kidney Diseases
Nephritis
Glomerulonephritis
Glomerulosclerosis, Focal Segmental
Renal Insufficiency
Renal Insufficiency, Chronic
Kidney Failure, Chronic
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Nephritis
Glomerulonephritis
Glomerulosclerosis, Focal Segmental
Renal Insufficiency
Renal Insufficiency, Chronic
Kidney Failure, Chronic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Genetic Diseases, Inborn
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Eye Diseases, Hereditary
Retinitis Pigmentosa
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Fragile X Syndrome
Heredodegenerative Disorders, Nervous System
Huntington Disease
Mental Retardation, X-Linked
Fragile X Syndrome
Myotonic Dystrophy
Spinocerebellar Degenerations
Myoclonic Cerebellar Dyssynergia
Olivopontocerebellar Atrophies
Spinocerebellar Ataxias
Machado-Joseph Disease
Muscular Dystrophies
Myotonic Dystrophy
Skin and Connective Tissue Diseases
Skin Diseases
Photosensitivity Disorders
Nutritional and Metabolic Diseases
Metabolic Diseases
Calcium Metabolism Disorders
Calcinosis
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Pathologic Processes
Chromosome Aberrations
Chromosomal Instability
Chromosome Fragility
Death
Cadaver
Disease
Syndrome
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Anticipation, Genetic
Diseases in Twins
Genomic Instability
Chromosomal Instability
Chromosome Fragility
Gliosis
Nerve Degeneration
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Athetosis
Chorea
Dystonia
Torticollis
Myoclonus
Tremor
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Intellectual Disability
Perceptual Disorders
Hallucinations
Psychomotor Disorders
Neuromuscular Manifestations
Muscular Atrophy
Paralysis
Paraplegia
Reflex, Abnormal
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