MeSH Treeview
Query OMIM entry list
606232
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CHROMOSOME 22q13.3 DELETION SYNDROME
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Sequence Homology
Sequence Homology, Nucleic Acid
Genetic Phenomena
Genetic Processes
DNA Damage
DNA Breaks
Chromosome Breakage
Gene Rearrangement
Mutagenesis
Sequence Deletion
Chromosome Deletion
Gene Deletion
Translocation, Genetic
Genetic Structures
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Chromosome Structures
Telomere
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 12
Chromosomes, Human, 13-15
Chromosomes, Human, Pair 13
Chromosomes, Human, 19-20
Chromosomes, Human, Pair 20
Chromosomes, Human, 21-22 and Y
Chromosomes, Human, Pair 22
Ring Chromosomes
Genetic Vectors
Cosmids
Genome
Genome Components
DNA, Intergenic
Introns
Genes
Gene Components
Exons
Introns
Tandem Repeat Sequences
Microsatellite Repeats
Plasmids
Cosmids
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosome Breakage
Ring Chromosomes
Translocation, Genetic
Sequence Deletion
Chromosome Deletion
Gene Deletion
Genotype
Haplotypes
Phenotype
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Sequence Homology
Sequence Homology, Nucleic Acid
Physiological Phenomena
Body Constitution
Body Weights and Measures
Body Size
Body Weight
Overweight
Obesity
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