"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) |
G05.090.403.180 G05.180
|
| Concept/Terms |
Consanguinous Mating- Consanguinous Mating
- Consanguinous Matings
- Mating, Consanguinous
- Matings, Consanguinous
- Inbreeding, Human
- Human Inbreeding
- Human Inbreedings
- Inbreedings, Human
Consanguineous Marriage- Consanguineous Marriage
- Consanguineous Marriages
- Marriage, Consanguineous
- Marriages, Consanguineous
|
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 this website 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 |
|---|
| 2001 | 0 | 1 | 1 |
| 2009 | 0 | 1 | 1 |
| 2012 | 0 | 1 | 1 |
| 2016 | 0 | 1 | 1 |
| 2017 | 0 | 11 | 11 |
| 2018 | 2 | 10 | 12 |
| 2019 | 1 | 1 | 2 |
| 2020 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Consanguinity" by people in Profiles.
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Gastrointestinal bleeding in a newborn infant with congenital factor X deficiency and COVID-19-A common clinical feature between a rare disorder and a new, common infection. Int J Lab Hematol. 2020 12; 42(6):e277-e279.
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COVID-19 reveals Brugada pattern in an adolescent patient. Cardiol Young. 2020 Nov; 30(11):1735-1737.
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Parental consanguinity in patients with psychogenic nonepileptic seizures. Epilepsy Behav. 2019 05; 94:167-168.
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Age of identification of sensorineural hearing loss and Characteristics of affected children: Findings from two cross-sectional studies in Saudi Arabia. Int J Pediatr Otorhinolaryngol. 2019 Jul; 122:27-34.
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IFN-? and CD25 drive distinct pathologic features during hemophagocytic lymphohistiocytosis. J Allergy Clin Immunol. 2019 06; 143(6):2215-2226.e7.
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A CIB1 Splice-Site Founder Mutation in Families with Typical Epidermodysplasia Verruciformis. J Invest Dermatol. 2019 05; 139(5):1195-1198.
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Assessment of coding region variants in Kuwaiti population: implications for medical genetics and population genomics. Sci Rep. 2018 11 08; 8(1):16583.
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Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability. Hum Genet. 2018 Sep; 137(9):735-752.
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Schizophrenia and co-morbid obsessive - compulsive disorder: Clinical characteristics. Asian J Psychiatr. 2018 Oct; 37:80-84.
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A novel in-frame deletion in ZMPSTE24 is associated with autosomal recessive acrogeria (Gottron type) in an extended consanguineous family. Clin Dysmorphol. 2018 Jul; 27(3):88-90.