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
CY
cytology
DI
diagnosis 5
DE
drug effects
ET
etiology
GE
genetics 8
IM
immunology
PA
pathology
PP
physiopathology 1
RE
radiation effects
UL
ultrastructure

C Diseases
C23 Pathological Conditions, Signs and Symptoms 451
C23.550 Pathologic Processes 195
C23.550.210 Chromosome Aberrations 1 574
C23.550.210.645 Nondisjunction, Genetic 7
C23.550.210.645.890 Uniparental Disomy 14

G Phenomena and Processes
G05 Genetic Phenomena 135
G05.365 Genetic Variation 858
G05.365.590 Mutation 4 997
G05.365.590.175 Chromosome Aberrations 1 574
G05.365.590.175.024 Abnormal Karyotype 19
G05.365.590.175.050 Aneuploidy 197
G05.365.590.175.125 Chimerism 30
G05.365.590.175.165 Chromosomal Instability 39
G05.365.590.175.175 Chromosome Breakage 26
G05.365.590.175.183 Chromosome Duplication 7
G05.365.590.175.190 Chromosome Inversion 18
G05.365.590.175.310 Chromothripsis 7
G05.365.590.175.430 Isochromosomes 2
G05.365.590.175.570 Micronuclei, Chromosome-Defective 31
G05.365.590.175.595 Mosaicism 118
G05.365.590.175.677 Polyploidy 139
G05.365.590.175.760 Ring Chromosomes 12
G05.365.590.175.815 Sex Chromosome Aberrations 28
G05.365.590.175.870 Translocation, Genetic 341
G05.365.590.175.935 Uniparental Disomy 14

Chromosome 1, uniparental disomy 1q12 q21 Disease MeSH Browser

Chromosome 10, uniparental disomy of Disease MeSH Browser

Chromosome 15, trisomy mosaicism Disease MeSH Browser

Chromosome 16, uniparental disomy Disease MeSH Browser

Chromosome 21, uniparental disomy of Disease MeSH Browser

Chromosome 5, uniparental disomy Disease MeSH Browser

Chromosome 7, trisomy mosaic Disease MeSH Browser

Chromosome 8, mosaic trisomy Disease MeSH Browser

Chromosome 9, trisomy mosaic Disease MeSH Browser

Trisomy 22 mosaicism syndrome Disease MeSH Browser

Uniparental disomy of 11 Disease MeSH Browser

Uniparental disomy of 13 Disease MeSH Browser

Uniparental disomy of chromosome 2 Disease MeSH Browser

Uniparental disomy, paternal, chromosome 14 Disease MeSH Browser

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