Aneuploidy [aneuploidie]

topical
197
Terms

aneuploidní buňka

 

Aneuploid
Aneuploid Cell

Persistent link   https://www.medvik.cz/link/D000782
Definition

The chromosomal constitution of cells which deviate from the normal by the addition or subtraction of CHROMOSOMES, chromosome pairs, or chromosome fragments. In a normally diploid cell (DIPLOIDY) the loss of a chromosome pair is termed nullisomy (symbol: 2N-2), the loss of a single chromosome is MONOSOMY (symbol: 2N-1), the addition of a chromosome pair is tetrasomy (symbol: 2N+2), the addition of a single chromosome is TRISOMY (symbol: 2N+1).

DUI
D000782 MeSH Browser
CUI
M0001173
Previous indexing
Chromosome Abnormalities (1966-1967)
History note
68
Public note
68

C Diseases
C23 Pathological Conditions, Signs and Symptoms 451
C23.550 Pathologic Processes 195
C23.550.210 Chromosome Aberrations 1 578
C23.550.210.024 Abnormal Karyotype 19
C23.550.210.050 Aneuploidy 197
C23.550.210.050.500 Monosomy 23
C23.550.210.050.625 Tetrasomy 2
C23.550.210.050.750 Trisomy 176
C23.550.210.110 Chromosomal Instability 40
C23.550.210.170 Chromosome Breakage 26
C23.550.210.182 Chromosome Duplication 7
C23.550.210.190 Chromosome Inversion 18
C23.550.210.310 Chromothripsis 7
C23.550.210.430 Isochromosomes 2
C23.550.210.570 Micronuclei, Chromosome-Defective 32
C23.550.210.645 Nondisjunction, Genetic 7
C23.550.210.702 Polyploidy 139
C23.550.210.760 Ring Chromosomes 12
C23.550.210.815 Sex Chromosome Aberrations 28
C23.550.210.870 Translocation, Genetic 343

G Phenomena and Processes
G05 Genetic Phenomena 135
G05.365 Genetic Variation 861
G05.365.590 Mutation 5 036
G05.365.590.175 Chromosome Aberrations 1 578
G05.365.590.175.024 Abnormal Karyotype 19
G05.365.590.175.050 Aneuploidy 197
G05.365.590.175.050.500 Monosomy 23
G05.365.590.175.050.625 Tetrasomy 2
G05.365.590.175.050.750 Trisomy 176
G05.365.590.175.125 Chimerism 30
G05.365.590.175.165 Chromosomal Instability 40
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 32
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 343
G05.365.590.175.935 Uniparental Disomy 14
G05.700 Ploidies 90
G05.700.131 Aneuploidy 197
G05.700.131.500 Monosomy 23
G05.700.131.625 Tetrasomy 2
G05.700.131.750 Trisomy 176
G05.700.264 Diploidy 143
G05.700.456 Haploidy 22
G05.700.740 Polyploidy 139

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Chromosome 15q, tetrasomy Disease MeSH Browser

Chromosome 18, tetrasomy 18p Disease MeSH Browser

Chromosome 21, tetrasomy 21q Disease MeSH Browser

Chromosome 9, duplication 9q21 Disease MeSH Browser

Chromosome 9, tetrasomy 9p Disease MeSH Browser

Schmid-Fraccaro syndrome Disease MeSH Browser

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