Descripteur en français: | Hétérogénéité génétique | ||||
Descripteur en anglais: | Genetic Heterogeneity | ||||
Descripteur en espagnol: |
Heterogeneidad Genética
| ||||
Descripteur en portugais: | Heterogeneidade Genética | ||||
Code(s) d'arborescence: |
G05.365.331 |
||||
Identificateur unique RDF: | https://id.nlm.nih.gov/mesh/D018740 | ||||
Note d'application: | 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) |
||||
Qualificatifs autorisés: |
DE effets des médicaments et des substances chimiques HI histoire RE effets des radiations |
||||
Identifiant DeCS: | 32225 | ||||
ID du Descripteur: | D018740 | ||||
Documents indexés dans la Biblioteque Virtuelle de Santé (BVS): | Cliquez ici pour accéder aux documents VHL | ||||
Date d'établissement: | 01/01/1995 | ||||
Date d'entrée: | 19/04/1994 | ||||
Date de révision: | 08/07/2008 |
-
-
PHÉNOMÈNES ET PROCESSUS
Phénomènes génétiques [G05]Phénomènes génétiques
|
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey