ONKI3 | Medical Subject Headings

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Genomic Instability

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Genomic Instability 79 coordinate concepts 2 subordinate concepts ∟ Chromosomal Instability \| ∟ Microsatellite Instability ∟ Acantholysis \| ∟ Adhesions \| ∟ Arrhythmia \| ∟ Ascites \| ∟ Azotemia \| ∟ Channelopathies \| ∟ Chromosome Aberrations \| ∟ Death \| ∟ Dehydration \| ∟ Delayed Graft Function \| ∟ Disease \| ∟ Disease Attributes \| ∟ Diverticulitis \| ∟ Emphysema \| ∟ Extravasation of Diagnostic and Therapeutic Materials \| ∟ Fibrosis \| ∟ Gliosis \| ∟ Granuloma \| ∟ Granulomatosis, Orofacial \| ∟ Growth Disorders \| ∟ Hemolysis \| ∟ Hemorrhage \| ∟ Hyperammonemia \| ∟ Hyperamylasemia \| ∟ Hyperbilirubinemia \| ∟ Hyperplasia \| ∟ Hyperuricemia \| ∟ Hypovolemia \| ∟ Inflammation \| ∟ Intraoperative Complications \| ∟ Leukoaraiosis \| ∟ Leukocytosis \| ∟ Lithiasis \| ∟ Malacoplakia \| ∟ Menstruation Disturbances \| ∟ Metaplasia \| ∟ Muscle Weakness \| ∟ Necrosis \| ∟ Neoplastic Processes \| ∟ Nerve Degeneration \| ∟ Ochronosis \| ∟ Ossification, Heterotopic \| ∟ Postoperative Complications \| ∟ Retropneumoperitoneum \| ∟ Sclerosis \| ∟ Shock \| ∟ Stress \| ∟ Ulcer \| ∟ Yang Deficiency \| ∟ Yin Deficiency \| ∟ Consanguinity \| ∟ Founder Effect \| ∟ Gene Frequency \| ∟ Gene Order \| ∟ Gene Pool \| ∟ Genetic Load \| ∟ Genotype \| ∟ Hybrid Vigor \| ∟ Inheritance Patterns \| ∟ Linkage (Genetics) \| ∟ Phenotype \| ∟ Phylogeny \| ∟ Ploidies \| ∟ Sequence Homology \| ∟ Sex Ratio \| ∟ Structural Homology, Protein \| ∟ Variation (Genetics) \| ∟ Allelic Imbalance \| ∟ Base Pair Mismatch \| ∟ Codon, Nonsense \| ∟ DNA Repeat Expansion \| ∟ Frameshift Mutation \| ∟ Gene Amplification \| ∟ Gene Duplication \| ∟ Germ-Line Mutation \| ∟ Mutation, Missense \| ∟ Point Mutation \| ∟ Sequence Deletion \| ∟ Suppression, Genetic Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Variation (Genetics) ∟ Mutation ∟ Genomic Instability 79 coordinate concepts 2 subordinate concepts ∟ Chromosomal Instability \| ∟ Microsatellite Instability ∟ Acantholysis \| ∟ Adhesions \| ∟ Arrhythmia \| ∟ Ascites \| ∟ Azotemia \| ∟ Channelopathies \| ∟ Chromosome Aberrations \| ∟ Death \| ∟ Dehydration \| ∟ Delayed Graft Function \| ∟ Disease \| ∟ Disease Attributes \| ∟ Diverticulitis \| ∟ Emphysema \| ∟ Extravasation of Diagnostic and Therapeutic Materials \| ∟ Fibrosis \| ∟ Gliosis \| ∟ Granuloma \| ∟ Granulomatosis, Orofacial \| ∟ Growth Disorders \| ∟ Hemolysis \| ∟ Hemorrhage \| ∟ Hyperammonemia \| ∟ Hyperamylasemia \| ∟ Hyperbilirubinemia \| ∟ Hyperplasia \| ∟ Hyperuricemia \| ∟ Hypovolemia \| ∟ Inflammation \| ∟ Intraoperative Complications \| ∟ Leukoaraiosis \| ∟ Leukocytosis \| ∟ Lithiasis \| ∟ Malacoplakia \| ∟ Menstruation Disturbances \| ∟ Metaplasia \| ∟ Muscle Weakness \| ∟ Necrosis \| ∟ Neoplastic Processes \| ∟ Nerve Degeneration \| ∟ Ochronosis \| ∟ Ossification, Heterotopic \| ∟ Postoperative Complications \| ∟ Retropneumoperitoneum \| ∟ Sclerosis \| ∟ Shock \| ∟ Stress \| ∟ Ulcer \| ∟ Yang Deficiency \| ∟ Yin Deficiency \| ∟ Consanguinity \| ∟ Founder Effect \| ∟ Gene Frequency \| ∟ Gene Order \| ∟ Gene Pool \| ∟ Genetic Load \| ∟ Genotype \| ∟ Hybrid Vigor \| ∟ Inheritance Patterns \| ∟ Linkage (Genetics) \| ∟ Phenotype \| ∟ Phylogeny \| ∟ Ploidies \| ∟ Sequence Homology \| ∟ Sex Ratio \| ∟ Structural Homology, Protein \| ∟ Variation (Genetics) \| ∟ Allelic Imbalance \| ∟ Base Pair Mismatch \| ∟ Codon, Nonsense \| ∟ DNA Repeat Expansion \| ∟ Frameshift Mutation \| ∟ Gene Amplification \| ∟ Gene Duplication \| ∟ Germ-Line Mutation \| ∟ Mutation, Missense \| ∟ Point Mutation \| ∟ Sequence Deletion \| ∟ Suppression, Genetic Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Pathologic Processes ∟ Genomic Instability 79 coordinate concepts 2 subordinate concepts ∟ Chromosomal Instability \| ∟ Microsatellite Instability ∟ Acantholysis \| ∟ Adhesions \| ∟ Arrhythmia \| ∟ Ascites \| ∟ Azotemia \| ∟ Channelopathies \| ∟ Chromosome Aberrations \| ∟ Death \| ∟ Dehydration \| ∟ Delayed Graft Function \| ∟ Disease \| ∟ Disease Attributes \| ∟ Diverticulitis \| ∟ Emphysema \| ∟ Extravasation of Diagnostic and Therapeutic Materials \| ∟ Fibrosis \| ∟ Gliosis \| ∟ Granuloma \| ∟ Granulomatosis, Orofacial \| ∟ Growth Disorders \| ∟ Hemolysis \| ∟ Hemorrhage \| ∟ Hyperammonemia \| ∟ Hyperamylasemia \| ∟ Hyperbilirubinemia \| ∟ Hyperplasia \| ∟ Hyperuricemia \| ∟ Hypovolemia \| ∟ Inflammation \| ∟ Intraoperative Complications \| ∟ Leukoaraiosis \| ∟ Leukocytosis \| ∟ Lithiasis \| ∟ Malacoplakia \| ∟ Menstruation Disturbances \| ∟ Metaplasia \| ∟ Muscle Weakness \| ∟ Necrosis \| ∟ Neoplastic Processes \| ∟ Nerve Degeneration \| ∟ Ochronosis \| ∟ Ossification, Heterotopic \| ∟ Postoperative Complications \| ∟ Retropneumoperitoneum \| ∟ Sclerosis \| ∟ Shock \| ∟ Stress \| ∟ Ulcer \| ∟ Yang Deficiency \| ∟ Yin Deficiency \| ∟ Consanguinity \| ∟ Founder Effect \| ∟ Gene Frequency \| ∟ Gene Order \| ∟ Gene Pool \| ∟ Genetic Load \| ∟ Genotype \| ∟ Hybrid Vigor \| ∟ Inheritance Patterns \| ∟ Linkage (Genetics) \| ∟ Phenotype \| ∟ Phylogeny \| ∟ Ploidies \| ∟ Sequence Homology \| ∟ Sex Ratio \| ∟ Structural Homology, Protein \| ∟ Variation (Genetics) \| ∟ Allelic Imbalance \| ∟ Base Pair Mismatch \| ∟ Codon, Nonsense \| ∟ DNA Repeat Expansion \| ∟ Frameshift Mutation \| ∟ Gene Amplification \| ∟ Gene Duplication \| ∟ Germ-Line Mutation \| ∟ Mutation, Missense \| ∟ Point Mutation \| ∟ Sequence Deletion \| ∟ Suppression, Genetic X
Broader terms:	Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Genomic Instability Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Variation (Genetics) ∟ Mutation ∟ Genomic Instability Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Pathologic Processes ∟ Genomic Instability Genetic Phenomena > Medical Subject Headings (MeSH) Mutation > Variation (Genetics) > Genetic Phenomena > Medical Subject Headings (MeSH) Pathologic Processes > Pathological Conditions, Signs and Symptoms > Medical Subject Headings (MeSH) X
Narrower terms:	Chromosomal Instability \| Microsatellite Instability X
historyNote*:	2004 X
publicMeSHNote*:	2004 X
Scope note:	An increased tendency of the GENOME to acquire MUTATIONS when various processes involved in maintaining and replicating the genome are dysfunctional. X
activeMeSHYear*:	2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	2003-07-09X
dateEstablished*:	2004-01-01X
Related term:	DNA Sequence, Unstable X
Type:	Concept X
Coordinate terms:	Acantholysis \| Adhesions \| Arrhythmia \| Ascites \| Azotemia \| Channelopathies \| Chromosome Aberrations \| Death \| Dehydration \| Delayed Graft Function \| Disease \| Disease Attributes \| Diverticulitis \| Emphysema \| Extravasation of Diagnostic and Therapeutic Materials \| Fibrosis \| Gliosis \| Granuloma \| Granulomatosis, Orofacial \| Growth Disorders \| Hemolysis \| Hemorrhage \| Hyperammonemia \| Hyperamylasemia \| Hyperbilirubinemia \| Hyperplasia \| Hyperuricemia \| Hypovolemia \| Inflammation \| Intraoperative Complications \| Leukoaraiosis \| Leukocytosis \| Lithiasis \| Malacoplakia \| Menstruation Disturbances \| Metaplasia \| Muscle Weakness \| Necrosis \| Neoplastic Processes \| Nerve Degeneration \| Ochronosis \| Ossification, Heterotopic \| Postoperative Complications \| Retropneumoperitoneum \| Sclerosis \| Shock \| Stress \| Ulcer \| Yang Deficiency \| Yin Deficiency \| Consanguinity \| Founder Effect \| Gene Frequency \| Gene Order \| Gene Pool \| Genetic Load \| Genotype \| Hybrid Vigor \| Inheritance Patterns \| Linkage (Genetics) \| Phenotype \| Phylogeny \| Ploidies \| Sequence Homology \| Sex Ratio \| Structural Homology, Protein \| Variation (Genetics) \| Allelic Imbalance \| Base Pair Mismatch \| Codon, Nonsense \| DNA Repeat Expansion \| Frameshift Mutation \| Gene Amplification \| Gene Duplication \| Germ-Line Mutation \| Mutation, Missense \| Point Mutation \| Sequence Deletion \| Suppression, Genetic X
URI:	X
Labels and equivalent concepts:	Perimän epästabiilius (fi) Perimän epävakaisuus (fi, replaced) Perimän instabiilius (fi, replaced) Genomin instabiilius (fi, replaced) Genomin epävakaisuus (fi, replaced) Genomin epästabiilius (fi, replaced) Genominstabilitet (sv) Genome Stability (en, replaced) Genome Instability (en, replaced) X
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