Chromosome Aberrations [chromozomální aberace]

topical
1 578
Terms

aberace chromozomu
aberace chromozomů
autozomální abnormality
chromosomové změny
chromozomální abnormality
chromozomová aberace
chromozomové aberace
chromozomové mutace
chromozomové změny
chromozómy - aberace
cytogenetické aberace
cytogenetické abnormality
cytogenetické změny

 

Abnormalities, Autosome
Abnormalities, Chromosomal
Abnormalities, Chromosome
Autosome Abnormalities
Chromosomal Aberrations
Chromosome Abnormalities
Cytogenetic Aberrations
Cytogenetic Abnormalities

Persistent link   https://www.medvik.cz/link/D002869
Definition

Abnormal number or structure of chromosomes. Chromosome aberrations may result in CHROMOSOME DISORDERS.

Annotation
coordinate IM with specific numbered chromosome or sex chromosome (IM) but not with CHROMOSOMES, HUMAN
DUI
D002869 MeSH Browser
CUI
M0004406
Previous indexing
Chromosome Abnormalities (1966-1967)
History note
1968; for CHROMOSOME ABNORMALITIES use CHROMOSOME ABERRATIONS 1963-2001 or CHROMOSOME DISORDERS 1963-2001; for AUTOSOME ABNORMALITIES use CHROMOSOME ABERRATIONS 1963-2001 or CHROMOSOME DISORDERS 1963-2001
Public note
1968; for CHROMOSOME ABNORMALITIES see CHROMOSOME ABNORMALITIES 1963-2001; for AUTOSOME ABNORMALITIES see CHROMOSOME ABNORMALITIES 1963-2001

Allowable subheadings

CI
chemically induced 39
CL
classification 42
DE
drug effects 48
EM
embryology 15
RE
radiation effects 37
SN
statistics & numerical data 23
VE
veterinary 1

C Diseases
C23 Pathological Conditions, Signs and Symptoms 451
C23.550 Pathologic Processes 195
C23.550.035 Acantholysis 10
C23.550.073 Arrhythmias, Cardiac 2 797
C23.550.081 Ascites 335
C23.550.113 Atrial Remodeling 13
C23.550.145 Azotemia 5
C23.550.161 Cardiotoxicity 142
C23.550.177 Channelopathies 14
C23.550.210 Chromosome Aberrations 1 578
C23.550.210.024 Abnormal Karyotype 19
C23.550.210.050 Aneuploidy 197
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
C23.550.260 Death 1 400
C23.550.274 Dehydration 403
C23.550.277 Delayed Graft Function 25
C23.550.288 Disease 1 712
C23.550.291 Disease Attributes 1 208
C23.550.308 Dysbiosis 107
C23.550.325 Emphysema 89
C23.550.340 Extravasation of Diagnostic and Therapeutic Materials 36
C23.550.347 Femoracetabular Impingement 27
C23.550.355 Fibrosis 366
C23.550.359 Frailty 122
C23.550.362 Genomic Instability 88
C23.550.369 Gliosis 37
C23.550.382 Granuloma 236
C23.550.384 Granulomatosis, Orofacial 6
C23.550.393 Growth Disorders 636
C23.550.403 Hemolysis 384
C23.550.414 Hemorrhage 2 296
C23.550.421 Hyperammonemia 31
C23.550.425 Hyperamylasemia 5
C23.550.429 Hyperbilirubinemia 184
C23.550.444 Hyperplasia 340
C23.550.449 Hyperuricemia 225
C23.550.455 Hypovolemia 87
C23.550.470 Inflammation 3 480
C23.550.505 Intraoperative Complications 717
C23.550.513 Ischemia 1 731
C23.550.522 Leukoaraiosis 4
C23.550.526 Leukocytosis 98
C23.550.537 Lithiasis 87
C23.550.543 Long Term Adverse Effects 7
C23.550.548 Malacoplakia 4
C23.550.568 Menstruation Disturbances 353
C23.550.589 Metaplasia 98
C23.550.695 Muscle Weakness 225
C23.550.706 Myotoxicity 1
C23.550.717 Necrosis 837
C23.550.722 Neointima 8
C23.550.727 Neoplastic Processes 130
C23.550.737 Nerve Degeneration 166
C23.550.744 Ochronosis 42
C23.550.751 Ossification, Heterotopic 139
C23.550.753 Ototoxicity 10
C23.550.755 Pigmentation Disorders 132
C23.550.759 Polydipsia 17
C23.550.767 Postoperative Complications 7 077
C23.550.770 Protein Aggregation, Pathological 16
C23.550.773 Respiratory Aspiration 79
C23.550.794 Retropneumoperitoneum 14
C23.550.823 Sclerosis 84
C23.550.835 Shock 410
C23.550.863 Teratogenesis 27
C23.550.877 Toxic Optic Neuropathy 1
C23.550.891 Ulcer 201
C23.550.918 Vascular Remodeling 29
C23.550.945 Yang Deficiency 9
C23.550.972 Yin Deficiency 9

G Phenomena and Processes
G05 Genetic Phenomena 135
G05.365 Genetic Variation 861
G05.365.590 Mutation 5 036
G05.365.590.029 Allelic Imbalance 2
G05.365.590.060 Base Pair Mismatch 14
G05.365.590.175 Chromosome Aberrations 1 578
G05.365.590.175.024 Abnormal Karyotype 19
G05.365.590.175.050 Aneuploidy 197
G05.365.590.175.125 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
G05.365.590.195 Codon, Nonsense 52
G05.365.590.220 DNA Repeat Expansion 7
G05.365.590.265 Frameshift Mutation 47
G05.365.590.288 Gain of Function Mutation 18
G05.365.590.310 Gene Amplification 334
G05.365.590.320 Gene Duplication 65
G05.365.590.335 Genomic Instability 88
G05.365.590.350 Germ-Line Mutation 202
G05.365.590.500 INDEL Mutation 17
G05.365.590.538 Loss of Function Mutation 13
G05.365.590.575 Mutagenesis, Insertional 56
G05.365.590.594 Mutation Accumulation 3
G05.365.590.612 Mutation Rate 18
G05.365.590.650 Mutation, Missense 216
G05.365.590.675 Point Mutation 246
G05.365.590.762 Sequence Deletion 104
G05.365.590.770 Sequence Inversion 2
G05.365.590.803 Silent Mutation 2
G05.365.590.835 Suppression, Genetic 29
G05.365.590.917 Synthetic Lethal Mutations 4

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