MeSH Treeview
Query OMIM entry list
302802
CMTX3
CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3
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High-scoring List
Genetic Phenomena
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 1
Chromosomes, Human, 16-18
Chromosomes, Human, Pair 17
Sex Chromosomes
X Chromosome
Genome
Genome Components
Genes
Genes, Recessive
Genes, X-Linked
Genetic Variation
Genetic Heterogeneity
Polymorphism, Genetic
Polymorphism, Restriction Fragment Length
Genotype
Haplotypes
Heterozygote
Inheritance Patterns
Genes, Recessive
Genes, X-Linked
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Database Center for Life Science
