MeSH Treeview
Query OMIM entry list
609260
CMT2A2
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2
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Chemical Phenomena
Biochemical Phenomena
Biochemical Processes
Carbohydrate Metabolism
Gluconeogenesis
Molecular Structure
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Chemical Processes
Biochemical Processes
Carbohydrate Metabolism
Gluconeogenesis
Metabolic Phenomena
Metabolism
Carbohydrate Metabolism
Gluconeogenesis
Genetic Phenomena
Gene Frequency
Genetic Processes
Mutagenesis
Amino Acid Substitution
Sequence Deletion
Recombination, Genetic
Genetic Structures
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 1
Genome
Genome Components
DNA, Intergenic
Introns
Genes
Alleles
Gene Components
Exons
Introns
Genes, Dominant
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Variation
Mutation
Mutation, Missense
Point Mutation
Sequence Deletion
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Genotype
Genetic Predisposition to Disease
Haplotypes
Inheritance Patterns
Genes, Dominant
Penetrance
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Penetrance
Physiological Phenomena
Electrophysiological Phenomena
Electrophysiological Processes
Neural Conduction
Physiological Processes
Electrophysiological Processes
Neural Conduction
Movement
Locomotion
Musculoskeletal and Neural Physiological Phenomena
Musculoskeletal Physiological Phenomena
Musculoskeletal Physiological Processes
Movement
Locomotion
Nervous System Physiological Phenomena
Nervous System Physiological Processes
Neural Conduction
Mathematical Concepts
Probability
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