MeSH Treeview
Query OMIM entry list
607831
CMT2K
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K
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Genetic Phenomena
Consanguinity
Founder Effect
Genetic Processes
Breeding
Inbreeding
Consanguinity
Genetic Structures
Genome
Genome Components
Genes
Genes, Recessive
Genetic Variation
Mutation
Chromosome Aberrations
Genotype
Haplotypes
Inheritance Patterns
Genes, Recessive
Genetic Linkage
Lod Score
Phenotype
Database Center for Life Science
