Translocation, Genetic [translokace genetická]

topical
341
Terms

chromozomální translokace
genetická translokace
translokace

 

Chromosomal Translocation
Translocation, Chromosomal

Persistent link   https://www.medvik.cz/link/D014178
Definition

A type of chromosome aberration characterized by CHROMOSOME BREAKAGE and transfer of the broken-off portion to another location, often to a different chromosome.

DUI
D014178 MeSH Browser
CUI
M0021829
Previous indexing
Chromosome Abnormalities (1966-1967); Chromosome Aberrations (1968-1974)
History note
2005(1968)
Public note
2005; see TRANSLOCATION (GENETICS) 1978-2005; see CHROMOSOME ABERRATIONS 1968-1977

Allowable subheadings

DE
drug effects 9
ES
ethics
GE
genetics 50
IM
immunology 6
PH
physiology 4
RE
radiation effects 1

C Diseases
C23 Pathological Conditions, Signs and Symptoms 451
C23.550 Pathologic Processes 195
C23.550.210 Chromosome Aberrations 1 574
C23.550.210.024 Abnormal Karyotype 19
C23.550.210.050 Aneuploidy 197
C23.550.210.110 Chromosomal Instability 39
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 31
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 341
C23.550.210.870.680 Philadelphia Chromosome 73

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
G05.365.590.175.870.680 Philadelphia Chromosome 73
G05.365.590.175.935 Uniparental Disomy 14
G05.558 Mutagenesis 276
G05.558.109 Amino Acid Substitution 176
G05.558.164 Chromosome Duplication 7
G05.558.220 DNA Repeat Expansion 7
G05.558.315 Gene Amplification 333
G05.558.320 Gene Duplication 65
G05.558.370 INDEL Mutation 17
G05.558.550 Mutagenesis, Insertional 56
G05.558.620 Nondisjunction, Genetic 7
G05.558.800 Sequence Deletion 104
G05.558.805 Sequence Inversion 2
G05.558.810 Somatic Hypermutation, Immunoglobulin 29
G05.558.835 Suppression, Genetic 29
G05.558.860 Translocation, Genetic 341

Chromosome 9 inversion or duplication Disease MeSH Browser

Chromosomes 1 and 2, monosomy 2q duplication 1p Disease MeSH Browser

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