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Query OMIM entry list
600202
DYX2
DYSLEXIA, SUSCEPTIBILITY TO, 2
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Cell Physiological Phenomena
Cell Physiological Processes
Cell Differentiation
Cell Movement
Cell Migration Inhibition
Genetic Phenomena
Gene Frequency
Genetic Processes
Gene Expression Regulation
Epigenesis, Genetic
Gene Silencing
RNA Interference
Mutagenesis
Sequence Deletion
Recombination, Genetic
Genetic Structures
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 2
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 6
Chromosomes, Human, 13-15
Chromosomes, Human, Pair 15
Chromosomes, Human, 16-18
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 18
Genome
Genome Components
Genes
Alleles
Gene Components
Genes, Dominant
Major Histocompatibility Complex
Genetic Loci
Major Histocompatibility Complex
Quantitative Trait Loci
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Variation
Genetic Heterogeneity
Mutation
Sequence Deletion
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Genotype
Genetic Predisposition to Disease
Haplotypes
Inheritance Patterns
Genes, Dominant
Quantitative Trait, Heritable
Genetic Linkage
Linkage Disequilibrium
Lod Score
Phenotype
Genetic Markers
Physiological Phenomena
Physiological Processes
Movement
Locomotion
Cell Movement
Immune System Phenomena
Immunogenetic Phenomena
Major Histocompatibility Complex
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