Uniparental Disomy [uniparentální disomie]
topical
14
- Terms
-
uniparentální dizomie
uniparentální dizómie
uniparentální heterodisomie
uniparentální heterodizomie
uniparentální heterodizómie
uniparentální isodisomie
uniparentální izodizomie
uniparentální izodizómie
-
Disomy, Uniparental
Uniparental Heterodisomy
Uniparental Isodisomy
Persistent link
https://www.medvik.cz/link/D024182
Definition
The presence in a cell of two paired chromosomes from the same parent, with no chromosome of that pair from the other parent. This chromosome composition stems from non-disjunction (NONDISJUNCTION, GENETIC) events during MEIOSIS. The disomy may be composed of both homologous chromosomes from one parent (heterodisomy) or a duplicate of one chromosome (isodisomy).
- DUI
- D024182 MeSH Browser
- CUI
- M0369518
- Previous indexing
- Aneuploidy (1980-2001); Chromosome Aberrations (1989-2001); Chromosome Abnormalities (1980-2001)
- History note
- 2002
- Public note
- 2002
Allowable subheadings
- CI
- chemically induced 0
- CY
- cytology 0
- DI
- diagnosis 5
- DE
- drug effects 0
- ET
- etiology 0
- GE
- genetics 8
- IM
- immunology 0
- PA
- pathology 0
- PP
- physiopathology 1
- RE
- radiation effects 0
- UL
- ultrastructure 0
...
Occurrences in Medvik records
C
Diseases
G
Phenomena and Processes