"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 |
|---|
| 2006 | 1 | 0 | 1 |
| 2012 | 0 | 2 | 2 |
| 2013 | 0 | 1 | 1 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Consanguinity" by people in Profiles.
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Associations of autozygosity with a broad range of human phenotypes. Nat Commun. 2019 10 31; 10(1):4957.
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Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India. Diabetes. 2013 May; 62(5):1746-55.
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A clinical evaluation tool for SNP arrays, especially for autosomal recessive conditions in offspring of consanguineous parents. Genet Med. 2013 May; 15(5):354-60.
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A novel mutation in the interleukin-1 receptor antagonist associated with intrauterine disease onset. Clin Immunol. 2012 Oct; 145(1):77-81.
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Novel homozygous, heterozygous and hemizygous FRMD7 gene mutations segregated in the same consanguineous family with congenital X-linked nystagmus. Eur J Hum Genet. 2012 Oct; 20(10):1032-6.
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Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred Arab family with an apparent autosomal dominant inheritance and reduced penetrance: clinical and genetic analysis. Am J Med Genet A. 2006 Jul 01; 140(13):1440-6.
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Multiple childhood osteosarcomas in an American Indian family with erythroid macrocytosis and skeletal anomalies. Cancer. 1977 Dec; 40(6):3115-22.