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602134
ETM2
TREMOR, HEREDITARY ESSENTIAL, 2
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Parkinsonian Disorders
Movement Disorders
Essential Tremor
Parkinsonian Disorders
Neurologic Manifestations
Dyskinesias
Tremor
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Tremor
Database Center for Life Science
