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Query OMIM entry list
609311
CMT4H
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Genetic Phenomena
Genetic Processes
Gene Expression
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 12
Chromosomes, Human, 13-15
Chromosomes, Human, Pair 13
Genome
Genome Components
Genes
Genes, Recessive
Genetic Variation
Mutation
Genotype
Genetic Predisposition to Disease
Homozygote
Inheritance Patterns
Genes, Recessive
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