 | 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).
Contents
- 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)
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.