"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.
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Year | Major Topic | Minor Topic | Total |
---|
1998 | 0 | 1 | 1 |
1999 | 0 | 2 | 2 |
2001 | 0 | 1 | 1 |
2005 | 0 | 1 | 1 |
2019 | 0 | 1 | 1 |
2020 | 0 | 1 | 1 |
2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Consanguinity" by people in Profiles.
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Consanguineous Blood Transfusion for Jehovah's Witness Child? Ann Thorac Surg. 2022 12; 114(6):2404-2405.
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Wiskott-Aldrich Syndrome in four male siblings from a consanguineous family from Lebanon. Clin Immunol. 2020 10; 219:108573.
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Mutations in KIRREL1, a slit diaphragm component, cause steroid-resistant nephrotic syndrome. Kidney Int. 2019 10; 96(4):883-889.
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Update on the prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency. J Pediatr Endocrinol Metab. 2005 Feb; 18(2):133-42.
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Apparent mineralocorticoid excess. Trends Endocrinol Metab. 2001 Apr; 12(3):104-11.
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Prevalence of mild apparent mineralocorticoid excess in Mennonites. J Clin Endocrinol Metab. 1999 Dec; 84(12):4735-8.
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Prenatal diagnosis and treatment of 11beta-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia. J Clin Endocrinol Metab. 1999 Sep; 84(9):3129-34.
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A genetic defect resulting in mild low-renin hypertension. Proc Natl Acad Sci U S A. 1998 Aug 18; 95(17):10200-5.