MeSH Treeview
Query OMIM entry list
600513
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EPILEPSY, NOCTURNAL FRONTAL LOBE, TYPE 1
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Physical Phenomena
Time
Periodicity
Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Sequence Homology
Sequence Homology, Amino Acid
Genetic Phenomena
Founder Effect
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 3
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 6
Chromosomes, Human, 13-15
Chromosomes, Human, Pair 15
Chromosomes, Human, 19-20
Chromosomes, Human, Pair 19
Chromosomes, Human, Pair 20
Genome
Genome Components
Genes
Gene Components
Exons
Genes, Dominant
Genetic Variation
Genetic Heterogeneity
Mutation
Mutation, Missense
Point Mutation
Polymorphism, Genetic
Polymorphism, Single-Stranded Conformational
Inheritance Patterns
Genes, Dominant
Penetrance
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Penetrance
Sequence Homology
Sequence Homology, Amino Acid
Physiological Phenomena
Chronobiology Phenomena
Periodicity
Circadian Rhythm
Musculoskeletal and Neural Physiological Phenomena
Nervous System Physiological Phenomena
Nervous System Physiological Processes
Sleep
Database Center for Life Science
