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Query OMIM entry list
607745
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SEIZURES, BENIGN FAMILIAL NEONATAL-INFANTILE
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High-scoring List
Genetic Phenomena
Founder Effect
Genetic Processes
Mutagenesis
Amino Acid Substitution
Recombination, Genetic
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 2
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 8
Chromosomes, Human, 19-20
Chromosomes, Human, Pair 19
Genome
Genome Components
Genes
Genes, Dominant
Genetic Variation
Genetic Heterogeneity
Mutation
Chromosome Aberrations
Mutation, Missense
Polymorphism, Genetic
Polymorphism, Single-Stranded Conformational
Genotype
Haplotypes
Inheritance Patterns
Genes, Dominant
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Biological Phenomena
Biological Processes
Remission, Spontaneous
Database Center for Life Science
