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Genetic Heterogeneity

"Genetic Heterogeneity" 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.

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The presence of apparently similar characters for which the genetic evidence indicates that different genes or different genetic mechanisms are involved in different pedigrees. In clinical settings genetic heterogeneity refers to the presence of a variety of genetic defects which cause the same disease, often due to mutations at different loci on the same gene, a finding common to many human diseases including ALZHEIMER DISEASE; CYSTIC FIBROSIS; LIPOPROTEIN LIPASE DEFICIENCY, FAMILIAL; and POLYCYSTIC KIDNEY DISEASES. (Rieger, et al., Glossary of Genetics: Classical and Molecular, 5th ed; Segen, Dictionary of Modern Medicine, 1992)


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This graph shows the total number of publications written about "Genetic Heterogeneity" by people in UAMS Profiles by year, and whether "Genetic Heterogeneity" was a major or minor topic of these publications.
Bar chart showing 15 publications over 13 distinct years, with a maximum of 2 publications in 2012 and 2018
To see the data from this visualization as text, click here.