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254800
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MYOCLONIC EPILEPSY OF UNVERRICHT AND LUNDBORG
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Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MERRF Syndrome
Muscular Disorders, Atrophic
Muscular Dystrophies
Myotonic Dystrophy
Myotonic Disorders
Myotonic Dystrophy
Digestive System Diseases
Liver Diseases
Porphyrias, Hepatic
Porphyria, Acute Intermittent
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
MERRF Syndrome
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Degenerations
Myoclonic Cerebellar Dyssynergia
Epilepsy
Epilepsies, Myoclonic
Myoclonic Epilepsies, Progressive
Lafora Disease
MERRF Syndrome
Unverricht-Lundborg Syndrome
Myoclonic Epilepsy, Juvenile
Epilepsy, Generalized
Epilepsy, Tonic-Clonic
Spasms, Infantile
Epilepsy, Reflex
Spinal Cord Diseases
Muscular Atrophy, Spinal
Spinal Muscular Atrophies of Childhood
Spinocerebellar Degenerations
Myoclonic Cerebellar Dyssynergia
Cranial Nerve Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Lafora Disease
Myotonic Dystrophy
Spinal Muscular Atrophies of Childhood
Spinocerebellar Degenerations
Myoclonic Cerebellar Dyssynergia
Unverricht-Lundborg Syndrome
Motor Neuron Disease
Muscular Atrophy, Spinal
Spinal Muscular Atrophies of Childhood
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Myoclonus
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Articulation Disorders
Dysarthria
Intellectual Disability
Reflex, Abnormal
Neuromuscular Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Spinal Muscular Atrophies of Childhood
Muscular Atrophy, Spinal
Spinal Muscular Atrophies of Childhood
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Myotonic Dystrophy
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MERRF Syndrome
Myotonic Disorders
Myotonic Dystrophy
Eye Diseases
Corneal Diseases
Corneal Opacity
Ocular Motility Disorders
Nystagmus, Pathologic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Lafora Disease
Myotonic Dystrophy
Spinal Muscular Atrophies of Childhood
Spinocerebellar Degenerations
Myoclonic Cerebellar Dyssynergia
Unverricht-Lundborg Syndrome
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
MERRF Syndrome
Porphyrias
Porphyrias, Hepatic
Porphyria, Acute Intermittent
Muscular Dystrophies
Myotonic Dystrophy
Skin Diseases, Genetic
Porphyrias, Hepatic
Porphyria, Acute Intermittent
Skin and Connective Tissue Diseases
Skin Diseases
Skin Diseases, Genetic
Porphyrias, Hepatic
Porphyria, Acute Intermittent
Skin Diseases, Metabolic
Porphyrias
Porphyrias, Hepatic
Porphyria, Acute Intermittent
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
MERRF Syndrome
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
MERRF Syndrome
Porphyrias
Porphyrias, Hepatic
Porphyria, Acute Intermittent
Mitochondrial Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MERRF Syndrome
Porphyrias
Porphyrias, Hepatic
Porphyria, Acute Intermittent
Skin Diseases, Metabolic
Porphyrias
Porphyrias, Hepatic
Porphyria, Acute Intermittent
Animal Diseases
Cattle Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Pathologic Processes
Chromosome Aberrations
Micronuclei, Chromosome-Defective
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Facies
Gliosis
Nerve Degeneration
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Myoclonus
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Articulation Disorders
Dysarthria
Intellectual Disability
Reflex, Abnormal
Substance-Related Disorders
Alcohol-Related Disorders
Alcoholic Intoxication
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