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601068
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EPILEPSY, MYOCLONIC, BENIGN ADULT FAMILIAL, TYPE 1
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Degenerations
Epilepsy
Epilepsies, Myoclonic
Epilepsy, Generalized
Epilepsy, Tonic-Clonic
Movement Disorders
Essential Tremor
Spinal Cord Diseases
Spinocerebellar Degenerations
Cranial Nerve Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Myoclonus
Tremor
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Articulation Disorders
Dysarthria
Intellectual Disability
Eye Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Pathologic Processes
Chromosome Aberrations
Disease
Syndrome
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Gliosis
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Myoclonus
Tremor
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Articulation Disorders
Dysarthria
Intellectual Disability
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