MeSH Treeview
Query OMIM entry list
608591
CMT2G
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2G
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High-scoring List
Genetic Phenomena
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 12
Genome
Genome Components
Genes
Genes, Dominant
Genotype
Haplotypes
Inheritance Patterns
Genes, Dominant
Genetic Linkage
Lod Score
Physiological Phenomena
Electrophysiological Phenomena
Electrophysiological Processes
Neural Conduction
Physiological Processes
Electrophysiological Processes
Neural Conduction
Movement
Locomotion
Musculoskeletal and Neural Physiological Phenomena
Musculoskeletal Physiological Phenomena
Musculoskeletal Physiological Processes
Movement
Locomotion
Nervous System Physiological Phenomena
Nervous System Physiological Processes
Neural Conduction
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