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133701
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EXOSTOSES, MULTIPLE, TYPE II
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Repetitive Sequences, Nucleic Acid
Sequence Homology
Sequence Homology, Amino Acid
Structure-Activity Relationship
Genetic Phenomena
Gene Frequency
Genetic Processes
Mutagenesis
Sequence Deletion
Chromosome Deletion
Gene Deletion
Recombination, Genetic
Genetic Structures
Base Sequence
Repetitive Sequences, Nucleic Acid
Chromosome Structures
Centromere
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 8
Chromosomes, Human, Pair 11
Chromosomes, Human, 19-20
Chromosomes, Human, Pair 19
Genome
Genome Components
DNA, Intergenic
Introns
Genes
Alleles
Gene Components
Exons
Introns
Genes, Dominant
Genes, Neoplasm
Genes, Tumor Suppressor
Genes, Recessive
Genes, Tumor Suppressor
Multigene Family
Genetic Variation
Genetic Heterogeneity
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Frameshift Mutation
Mutation, Missense
Point Mutation
Sequence Deletion
Chromosome Deletion
Gene Deletion
Polymorphism, Genetic
Polymorphism, Single-Stranded Conformational
Genotype
Heterozygote
Inheritance Patterns
Genes, Dominant
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Sequence Homology
Sequence Homology, Amino Acid
Physiological Phenomena
Pharmacological Phenomena
Structure-Activity Relationship
Database Center for Life Science
