MeSH Treeview
Query OMIM entry list
607677
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CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Base Sequence
Genetic Phenomena
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 16-18
Chromosomes, Human, Pair 17
Genome
Genome Components
Genes
Multigene Family
Genetic Variation
Mutation
Mutation, Missense
Point Mutation
Genotype
Genetic Predisposition to Disease
Genetic Linkage
Phenotype
Database Center for Life Science