MeSH Treeview
Query OMIM entry list
607876
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EPILEPSY, MYOCLONIC, BENIGN ADULT FAMILIAL, TYPE 2
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High-scoring List
Genetic Phenomena
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 2
Genome
Genome Components
Genes
Alleles
Genes, Dominant
Genetic Variation
Genetic Heterogeneity
Inheritance Patterns
Genes, Dominant
Genetic Linkage
Lod Score
Physiological Phenomena
Electrophysiological Phenomena
Evoked Potentials
Evoked Potentials, Somatosensory
Evoked Potentials, Visual
Musculoskeletal and Neural Physiological Phenomena
Nervous System Physiological Phenomena
Evoked Potentials
Evoked Potentials, Somatosensory
Evoked Potentials, Visual
Nervous System Physiological Processes
Reflex
Ocular Physiological Phenomena
Evoked Potentials, Visual
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