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190300
ETM1
TREMOR, HEREDITARY ESSENTIAL, 1
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Digestive System Diseases
Liver Diseases
Hepatolenticular Degeneration
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Dystonia Musculorum Deformans
Hepatolenticular Degeneration
Parkinsonian Disorders
Parkinson Disease
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hepatolenticular Degeneration
Movement Disorders
Dystonic Disorders
Dystonia Musculorum Deformans
Essential Tremor
Hepatolenticular Degeneration
Parkinsonian Disorders
Parkinson Disease
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Dystonia Musculorum Deformans
Hepatolenticular Degeneration
Parkinson Disease
Neurologic Manifestations
Dyskinesias
Dystonia
Tremor
Neurobehavioral Manifestations
Memory Disorders
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
Heredodegenerative Disorders, Nervous System
Dystonia Musculorum Deformans
Hepatolenticular Degeneration
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hepatolenticular Degeneration
Metal Metabolism, Inborn Errors
Hepatolenticular Degeneration
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hepatolenticular Degeneration
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hepatolenticular Degeneration
Metal Metabolism, Inborn Errors
Hepatolenticular Degeneration
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Pathologic Processes
Chromosome Aberrations
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Diseases in Twins
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Dystonia
Tremor
Neurobehavioral Manifestations
Memory Disorders
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