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Query OMIM entry list
211750
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C SYNDROME
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Base Sequence
Cell Physiological Phenomena
Cell Physiological Processes
Cell Adhesion
Genetic Phenomena
Genetic Processes
Gene Expression
Mutagenesis
Sequence Deletion
Chromosome Deletion
Translocation, Genetic
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 3
Chromosomes, Human, 4-5
Chromosomes, Human, Pair 4
Chromosomes, Human, Pair 5
Genome
Genome Components
Genes
Genes, Dominant
Genes, Recessive
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Trisomy
Chromosome Duplication
Trisomy
Translocation, Genetic
Mutation, Missense
Sequence Deletion
Chromosome Deletion
Inheritance Patterns
Genes, Dominant
Genes, Recessive
Phenotype
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Trisomy
Musculoskeletal and Neural Physiological Phenomena
Musculoskeletal Physiological Phenomena
Psychomotor Performance
Nervous System Physiological Phenomena
Psychomotor Performance
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