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606350
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Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Muscle Weakness
Nervous System Diseases
Autonomic Nervous System Diseases
Primary Dysautonomias
Multiple System Atrophy
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Multiple System Atrophy
Brain Diseases, Metabolic
Mitochondrial Encephalomyopathies
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Ataxias
Ataxia Telangiectasia
Spinocerebellar Degenerations
Epilepsy
Seizures
Movement Disorders
Multiple System Atrophy
Ocular Motility Disorders
Spinal Cord Diseases
Spinocerebellar Degenerations
Cranial Nerve Diseases
Ocular Motility Disorders
Oculomotor Nerve Diseases
Oculomotor Nerve Diseases
Neurocutaneous Syndromes
Ataxia Telangiectasia
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Multiple System Atrophy
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Spinocerebellar Ataxias
Ataxia Telangiectasia
Dystonia
Neurobehavioral Manifestations
Psychomotor Disorders
Apraxias
Neuromuscular Manifestations
Muscle Weakness
Seizures
Sensation Disorders
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Peripheral Nervous System Diseases
Eye Diseases
Ocular Motility Disorders
Oculomotor Nerve Diseases
Cardiovascular Diseases
Vascular Diseases
Telangiectasis
Ataxia Telangiectasia
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Protein Disorders
Hypoproteinemia
Hypoalbuminemia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Ataxia Telangiectasia
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Hyperlipoproteinemia Type II
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Mitochondrial Encephalomyopathies
DNA Repair-Deficiency Disorders
Ataxia Telangiectasia
Lipid Metabolism Disorders
Dyslipidemias
Hyperlipidemias
Hyperlipoproteinemias
Hyperlipoproteinemia Type II
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Hyperlipoproteinemia Type II
Mitochondrial Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Endocrine System Diseases
Immune System Diseases
Immunologic Deficiency Syndromes
Ataxia Telangiectasia
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Pathologic Processes
Disease
Syndrome
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Muscle Weakness
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Dystonia
Neurobehavioral Manifestations
Apraxias
Psychomotor Disorders
Apraxias
Neuromuscular Manifestations
Muscle Weakness
Seizures
Sensation Disorders
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