Consanguinity
"Consanguinity" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The magnitude of INBREEDING in humans.
| Descriptor ID |
D003241
|
| MeSH Number(s) |
G05.180 G05.355.090.403.180
|
| Concept/Terms |
Consanguinous Mating- Consanguinous Mating
- Consanguinous Matings
- Mating, Consanguinous
- Matings, Consanguinous
- Inbreeding, Human
- Human Inbreeding
- Human Inbreedings
- Inbreedings, Human
|
Below are MeSH descriptors whose meaning is more general than "Consanguinity".
Below are MeSH descriptors whose meaning is more specific than "Consanguinity".
This graph shows the total number of publications written about "Consanguinity" by people in UAMS Profiles by year, and whether "Consanguinity" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2017 | 0 | 1 | 1 |
| 2014 | 0 | 1 | 1 |
| 2012 | 1 | 0 | 1 |
| 2009 | 0 | 1 | 1 |
| 2008 | 0 | 3 | 3 |
| 2007 | 0 | 1 | 1 |
| 2005 | 0 | 1 | 1 |
| 2002 | 0 | 1 | 1 |
| 2001 | 0 | 1 | 1 |
| 1994 | 0 | 1 | 1 |
| 1989 | 1 | 1 | 2 |
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Below are the most recent publications written about "Consanguinity" by people in Profiles over the past ten years.
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Hardin JS, Schaefer GB, Sallam AB, Williams MK, Uwaydat S. A unique case series of autosomal recessive bestrophinopathy exhibiting multigenerational inheritance. Ophthalmic Genet. 2017 12; 38(6):570-574.