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601462
SCCMS
MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL
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Physical Phenomena
Biophysical Phenomena
Membrane Potentials
Chemical Phenomena
Biochemical Phenomena
Biochemical Processes
Signal Transduction
Ion Channel Gating
Molecular Structure
Amino Acid Sequence
Base Sequence
Binding Sites
Molecular Conformation
Protein Conformation
Sequence Homology
Sequence Homology, Amino Acid
Chemical Processes
Biochemical Processes
Signal Transduction
Ion Channel Gating
Cell Physiological Phenomena
Cell Physiological Processes
Ion Channel Gating
Signal Transduction
Ion Channel Gating
Membrane Potentials
Action Potentials
Genetic Phenomena
Genetic Processes
Gene Expression Regulation
Gene Amplification
Mutagenesis
Gene Amplification
Recombination, Genetic
Transfection
Genetic Structures
Base Sequence
Genetic Code
Codon
Genome
Genome Components
Genes
Alleles
Gene Components
Codon
Exons
Genes, Dominant
Genetic Variation
Genetic Heterogeneity
Mutation
Gene Amplification
Mutation, Missense
Point Mutation
Polymorphism, Genetic
Polymorphism, Single-Stranded Conformational
Genotype
Genetic Predisposition to Disease
Heterozygote
Inheritance Patterns
Genes, Dominant
Sequence Homology
Sequence Homology, Amino Acid
Physiological Phenomena
Electrophysiological Phenomena
Electrophysiological Processes
Ion Channel Gating
Neural Conduction
Membrane Potentials
Action Potentials
Physiological Processes
Electrophysiological Processes
Ion Channel Gating
Neural Conduction
Reproductive and Urinary Physiological Phenomena
Reproductive Physiological Phenomena
Reproductive Physiological Processes
Reproduction
Pregnancy
Musculoskeletal and Neural Physiological Phenomena
Nervous System Physiological Phenomena
Membrane Potentials
Action Potentials
Nervous System Physiological Processes
Neural Conduction
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