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118300
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CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Molecular Conformation
Protein Conformation
Protein Structure, Tertiary
Genetic Phenomena
Genetic Processes
Mutagenesis
Sequence Deletion
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 1
Chromosomes, Human, 16-18
Chromosomes, Human, Pair 17
Genome
Genome Components
Genes
Genes, Dominant
Genetic Variation
Mutation
Point Mutation
Sequence Deletion
Genotype
Haplotypes
Inheritance Patterns
Genes, Dominant
Genetic Linkage
Phenotype
Physiological Phenomena
Electrophysiological Phenomena
Electrophysiological Processes
Neural Conduction
Evoked Potentials
Evoked Potentials, Auditory
Physiological Processes
Electrophysiological Processes
Neural Conduction
Circulatory and Respiratory Physiological Phenomena
Cardiovascular Physiological Phenomena
Hemodynamics
Blood Pressure
Musculoskeletal and Neural Physiological Phenomena
Nervous System Physiological Phenomena
Evoked Potentials
Evoked Potentials, Auditory
Nervous System Physiological Processes
Neural Conduction
Reflex
Reflex, Abnormal
Sensation
Hearing
Otoacoustic Emissions, Spontaneous
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