MeSH Treeview
Query OMIM entry list
607731
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CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H
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Genetic Phenomena
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 8
Genome
Genome Components
Genes
Genes, Recessive
Genotype
Haplotypes
Inheritance Patterns
Genes, Recessive
Genetic Linkage
Phenotype
Genetic Markers
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