MeSH Treeview
Query OMIM entry list
607684
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CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Phenomena
Genetic Processes
Mutagenesis
Amino Acid Substitution
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 8
Genome
Genome Components
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Variation
Mutation
Mutation, Missense
Point Mutation
Polymorphism, Genetic
Polymorphism, Single-Stranded Conformational
Genetic Linkage
Lod Score
Database Center for Life Science