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Query OMIM entry list
600858
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CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, WITH WOLFF-PARKINSON-WHITE SYNDROME
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Conserved Sequence
Sequence Homology
Sequence Homology, Amino Acid
Genetic Phenomena
Gene Frequency
Genetic Processes
Mutagenesis
Sequence Deletion
Recombination, Genetic
Transformation, Genetic
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 7
Genetic Code
Codon
Genome
Genome Components
DNA, Intergenic
Introns
Genes
Alleles
Gene Components
Codon
Exons
Introns
Genes, Fungal
Genome, Fungal
Genes, Fungal
Genetic Variation
Mutation
Mutation, Missense
Sequence Deletion
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Genotype
Genetic Predisposition to Disease
Heterozygote
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Sequence Homology
Sequence Homology, Amino Acid
Mathematical Concepts
Sensitivity and Specificity
Database Center for Life Science
