List of MeSH codes (G13)
This article needs to be updated. The reason given is: no files for 2006 are listed at the cited source, but files for 2013 are there; NLM releases this information annually.(February 2020) |
The following is a partial list of the "G" codes for Medical Subject Headings (MeSH), as defined by the United States National Library of Medicine (NLM).
This list continues the information at List of MeSH codes (G12). Codes following these are found at List of MeSH codes (G14). For other MeSH codes, see List of MeSH codes.
The source for this content is the set of 2006 MeSH Trees from the NLM.
MeSH G13 – []
MeSH G13.180 – consanguinity[]
MeSH G13.285 – founder effect[]
MeSH G13.330 – gene frequency[]
- MeSH G13.330.159 – gene flow
- MeSH G13.330.320 – genetic drift
MeSH G13.340 – gene order[]
MeSH G13.345 – gene pool[]
MeSH G13.360 – genetic load[]
MeSH G13.370 – genomic instability[]
MeSH G13.380 – genotype[]
- MeSH G13.380.350 – gene dosage
- MeSH G13.380.355 –
- MeSH G13.380.360 – haplotypes
- MeSH G13.380.383 – heterozygote
- MeSH G13.380.554 – homozygote
MeSH G13.400 – hybrid vigor[]
MeSH G13.420 – []
- MeSH G13.420.040 – anticipation, genetic
- MeSH G13.420.275 –
- MeSH G13.420.275.500 – genes, mitochondrial
- MeSH G13.420.320 – genes, dominant
- MeSH G13.420.325 – genes, recessive
- MeSH G13.420.457 –
- MeSH G13.420.523 –
- MeSH G13.420.590 – multifactorial inheritance
- MeSH G13.420.720 –
MeSH G13.540 – linkage (genetics)[]
- MeSH G13.540.500 – linkage disequilibrium
- MeSH G13.540.562 – lod score
MeSH G13.695 – phenotype[]
- MeSH G13.695.450 – genetic markers
- MeSH G13.695.650 – penetrance
MeSH G13.697 – phylogeny[]
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 G13.815 – sex ratio[]
MeSH G13.820 – structural homology, protein[]
MeSH G13.920 – variation (genetics)[]
- MeSH G13.920.036 –
- MeSH G13.920.073 – antigenic variation
- MeSH G13.920.331 – genetic heterogeneity
- MeSH G13.920.590 – mutation
- MeSH G13.920.590.029 –
- MeSH G13.920.590.029.530 – loss of heterozygosity
- MeSH G13.920.590.029.530.175 – chromosome deletion
- MeSH G13.920.590.060 –
- 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 –
- MeSH G13.920.590.175.175 –
- 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 –
- 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 –
- MeSH G13.920.590.675 – point mutation
- MeSH G13.920.590.762 –
- MeSH G13.920.590.762.180 – chromosome deletion
- MeSH G13.920.590.762.320 – gene deletion
- MeSH G13.920.590.835 –
- MeSH G13.920.795 –
- MeSH G13.920.795.595 –
- MeSH G13.920.795.600 –
- MeSH G13.920.795.800 –
The list continues at List of MeSH codes (G14).
Categories:
- Medical Subject Headings