List of MeSH codes (G13)

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 – genetic phenomena

MeSH G13.180 – consanguinity

MeSH G13.285 – founder effect

MeSH G13.330 – gene frequency

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 G13.400 – hybrid vigor

MeSH G13.420 – inheritance patterns

MeSH G13.540 – linkage (genetics)

MeSH G13.695 – phenotype

MeSH G13.697 – phylogeny

MeSH G13.700 – ploidies

MeSH G13.810 – sequence homology

MeSH G13.815 – sex ratio

MeSH G13.820 – structural homology, protein

MeSH G13.920 – variation (genetics)

The list continues at List of MeSH codes (G14).

gollark: Each "tick", though, do the new actions replace the old ones or what?
gollark: Hmm, seems good, very functional programming ish.
gollark: I mean, it could also detect non-blue things.
gollark: Thus, object detection?
gollark: Oh, neat.
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