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158170
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MONOSOMY 9p SYNDROME
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Phenomena
Genetic Processes
Mutagenesis
Sequence Deletion
Chromosome Deletion
Gene Deletion
Translocation, Genetic
Sex Determination Processes
Genetic Structures
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 9
Sex Chromosomes
X Chromosome
Y Chromosome
Genome
Genome Components
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Trisomy
Chromosome Duplication
Trisomy
Translocation, Genetic
Sequence Deletion
Chromosome Deletion
Gene Deletion
Phenotype
Genetic Markers
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Trisomy
Physiological Phenomena
Physiological Processes
Growth and Development
Morphogenesis
Embryonic and Fetal Development
Organogenesis
Sex Determination Processes
Sexual Development
Sex Determination Processes
Reproductive and Urinary Physiological Phenomena
Reproductive Physiological Phenomena
Reproductive Physiological Processes
Sexual Development
Sex Determination Processes
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