MeSH Tree Structures - 2008

G13 - Genetic Phenomena

• Genetic Phenomena [G13]
  • Consanguinity [G13.180]
  • Founder Effect [G13.285]
  • Gene Frequency [G13.330]
    • Gene Flow [G13.330.159]
    • Genetic Drift [G13.330.320]
  • Gene Order [G13.340]
  • Gene Pool [G13.345]
  • Genetic Load [G13.360]
  • Genomic Instability [G13.370]
    • Chromosomal Instability [G13.370.180]
      • Chromosome Fragility [G13.370.180.180]
    • Microsatellite Instability [G13.370.590]
  • Genotype [G13.380]
    • Gene Dosage [G13.380.350]
    • Genetic Predisposition to Disease [G13.380.355]
    • Haplotypes [G13.380.360]
    • Heterozygote [G13.380.383]
    • Homozygote [G13.380.554]
  • Hybrid Vigor [G13.400]
  • Inheritance Patterns [G13.420]
    • Anticipation, Genetic [G13.420.040]
    • Extrachromosomal Inheritance [G13.420.275]
      • Genes, Mitochondrial [G13.420.275.500]
    • Genes, Dominant [G13.420.320]
    • Genes, Recessive [G13.420.325]
    • Genes, X-Linked [G13.420.457]
    • Genes, Y-Linked [G13.420.523]
    • Multifactorial Inheritance [G13.420.590]
    • Quantitative Trait, Heritable [G13.420.720]
  • Linkage (Genetics) [G13.540]
    • Linkage Disequilibrium [G13.540.500]
    • Lod Score [G13.540.562]
  • Phenotype [G13.695]
    • Genetic Markers [G13.695.450]
    • Penetrance [G13.695.650]
  • Phylogeny [G13.697]
  • Ploidies [G13.700]
    • Aneuploidy [G13.700.131]
      • Monosomy [G13.700.131.500]
      • Trisomy [G13.700.131.750]
    • Diploidy [G13.700.264]
    • Haploidy [G13.700.456]
    • Polyploidy [G13.700.740]
  • Sequence Homology [G13.810]
    • Sequence Homology, Amino Acid [G13.810.200]
    • Sequence Homology, Nucleic Acid [G13.810.550]
      • Synteny [G13.810.550.830]
  • Sex Ratio [G13.815]
  • Structural Homology, Protein [G13.820]
  • Variation (Genetics) [G13.920]
    • Antibody Diversity [G13.920.036]
    • Antigenic Variation [G13.920.073]
    • Genetic Heterogeneity [G13.920.331]
    • Mutation [G13.920.590]
      • Allelic Imbalance [G13.920.590.029]
        • Loss of Heterozygosity [G13.920.590.029.530]
          • Chromosome Deletion [G13.920.590.029.530.175]
      • Base Pair Mismatch [G13.920.590.060]
      • Chromosome Aberrations [G13.920.590.175]
        • Aneuploidy [G13.920.590.175.050]
          • Monosomy [G13.920.590.175.050.500]
          • Trisomy [G13.920.590.175.050.750]
        • Chimerism [G13.920.590.175.125]
        • Chromosomal Instability [G13.920.590.175.165]
          • Chromosome Fragility [G13.920.590.175.165.180]
        • Chromosome Breakage [G13.920.590.175.175]
        • Chromosome Deletion [G13.920.590.175.177]
        • Inversion, Chromosome [G13.920.590.175.420]
        • Isochromosomes [G13.920.590.175.430]
        • Micronuclei, Chromosome-Defective [G13.920.590.175.570]
        • Mosaicism [G13.920.590.175.595]
        • Ring Chromosomes [G13.920.590.175.760]
        • Sex Chromosome Aberrations [G13.920.590.175.815]
          • XYY Karyotype [G13.920.590.175.815.970]
        • Translocation, Genetic [G13.920.590.175.870]
          • Philadelphia Chromosome [G13.920.590.175.870.680]
        • Uniparental Disomy [G13.920.590.175.935]
      • Codon, Nonsense [G13.920.590.195]
      • DNA Repeat Expansion [G13.920.590.220]
        • Trinucleotide Repeat Expansion [G13.920.590.220.865]
      • Frameshift Mutation [G13.920.590.265]
      • Gene Amplification [G13.920.590.310]
      • Gene Duplication [G13.920.590.320]
      • Genomic Instability [G13.920.590.335]
        • Microsatellite Instability [G13.920.590.335.590]
      • Germ-Line Mutation [G13.920.590.350]
      • INDEL Mutation [G13.920.590.500]
      • Mutagenesis, Insertional [G13.920.590.575]
      • Mutation, Missense [G13.920.590.650]
      • Point Mutation [G13.920.590.675]
      • Sequence Deletion [G13.920.590.762]
        • Chromosome Deletion [G13.920.590.762.180]
        • Gene Deletion [G13.920.590.762.320]
      • Suppression, Genetic [G13.920.590.835]
    • Polymorphism, Genetic [G13.920.795]
      • Polymorphism, Restriction Fragment Length [G13.920.795.595]
      • Polymorphism, Single Nucleotide [G13.920.795.598]
      • Polymorphism, Single-Stranded Conformational [G13.920.795.600]

Last updated: 08 October 2007
First published: 08 October 2007
Metadata| Permanence level: Permanent: Dynamic Content