MeSH Treeview
Query OMIM entry list
608673
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CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Phenomena
Genetic Structures
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 12
Genome
Genome Components
Genes
Genes, Dominant
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Variation
Mutation
Mutation, Missense
Genotype
Haplotypes
Inheritance Patterns
Genes, Dominant
Genetic Linkage
Lod Score
Database Center for Life Science
