List of MeSH codes (G13)
- For other categories, see List of MeSH codes.
The following is a list of the "G" codes for MeSH. It is a product of the United States National Library of Medicine.
Source for content is here. (File "2006 MeSH Trees".)
MeSH G13 --- genetic phenomena
MeSH G13.330 --- gene frequency
- MeSH G13.330.159 --- gene flow
- MeSH G13.330.320 --- genetic drift
MeSH G13.370 --- genomic instability
- MeSH G13.370.180 --- chromosome instability
- MeSH G13.370.180.180 --- chromosome fragility
MeSH G13.380 --- genotype
- MeSH G13.380.350 --- gene dosage
- MeSH G13.380.355 --- genetic predisposition to disease
- MeSH G13.380.360 --- haplotypes
- MeSH G13.380.383 --- heterozygote
- MeSH G13.380.554 --- homozygote
MeSH G13.420 --- inheritance patterns
- MeSH G13.420.040 --- anticipation, genetic
- MeSH G13.420.275 --- extrachromosomal inheritance
- MeSH G13.420.275.500 --- genes, mitochondrial
- MeSH G13.420.320 --- genes, dominant
- MeSH G13.420.325 --- genes, recessive
- MeSH G13.420.457 --- genes, x-linked
- MeSH G13.420.523 --- genes, y-linked
- MeSH G13.420.590 --- multifactorial inheritance
- MeSH G13.420.720 --- quantitative trait, heritable
MeSH G13.540 --- linkage (genetics)
MeSH G13.695 --- phenotype
MeSH G13.700 --- ploidies
- MeSH G13.700.131 --- aneuploidy
- MeSH G13.700.131.500 --- monosomy
- MeSH G13.700.131.750 --- trisomy
- MeSH G13.700.264 --- diploidy
- MeSH G13.700.456 --- haploidy
- MeSH G13.700.740 --- polyploidy
MeSH G13.810 --- sequence homology
- MeSH G13.810.200 --- sequence homology, amino acid
- MeSH G13.810.550 --- sequence homology, nucleic acid
- MeSH G13.810.550.830 --- synteny
MeSH G13.920 --- variation (genetics)
- MeSH G13.920.036 --- antibody diversity
- MeSH G13.920.073 --- antigenic variation
- MeSH G13.920.331 --- genetic heterogeneity
- MeSH G13.920.590 --- mutation
- MeSH G13.920.590.029 --- allelic imbalance
- MeSH G13.920.590.029.530 --- loss of heterozygosity
- MeSH G13.920.590.029.530.175 --- chromosome deletion
- MeSH G13.920.590.060 --- base pair mismatch
- MeSH G13.920.590.120 --- codon, nonsense
- MeSH G13.920.590.175 --- chromosome aberrations
- MeSH G13.920.590.175.050 --- aneuploidy
- MeSH G13.920.590.175.050.500 --- monosomy
- MeSH G13.920.590.175.050.750 --- trisomy
- MeSH G13.920.590.175.125 --- chimerism
- MeSH G13.920.590.175.165 --- chromosomal instability
- MeSH G13.920.590.175.165.180 --- chromosome fragility
- MeSH G13.920.590.175.175 --- chromosome breakage
- MeSH G13.920.590.175.177 --- chromosome deletion
- MeSH G13.920.590.175.420 --- inversion, chromosome
- MeSH G13.920.590.175.430 --- isochromosomes
- MeSH G13.920.590.175.570 --- micronuclei, chromosome-defective
- MeSH G13.920.590.175.595 --- mosaicism
- MeSH G13.920.590.175.760 --- ring chromosomes
- MeSH G13.920.590.175.815 --- sex chromosome aberrations
- MeSH G13.920.590.175.815.970 --- xyy karyotype
- MeSH G13.920.590.175.870 --- translocation, genetic
- MeSH G13.920.590.175.870.680 --- philadelphia chromosome
- MeSH G13.920.590.175.935 --- uniparental disomy
- MeSH G13.920.590.220 --- dna repeat expansion
- MeSH G13.920.590.220.865 --- trinucleotide repeat expansion
- MeSH G13.920.590.300 --- frameshift mutation
- MeSH G13.920.590.310 --- gene amplification
- MeSH G13.920.590.320 --- gene duplication
- MeSH G13.920.590.335 --- genomic instability
- MeSH G13.920.590.350 --- germline mutation
- MeSH G13.920.590.650 --- mutation, missense
- MeSH G13.920.590.675 --- point mutation
- MeSH G13.920.590.762 --- sequence deletion
- MeSH G13.920.590.762.180 --- chromosome deletion
- MeSH G13.920.590.762.320 --- gene deletion
- MeSH G13.920.590.835 --- suppression, genetic
- MeSH G13.920.795 --- polymorphism, genetic
- MeSH G13.920.795.595 --- polymorphism, restriction fragment length
- MeSH G13.920.795.600 --- polymorphism, single-stranded conformational
- MeSH G13.920.795.800 --- polymorphism, single nucleotide
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