ONKI3 | Medical Subject Headings

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Ploidies ∟ Aneuploidy 16 coordinate concepts 2 subordinate concepts ∟ Monosomy \| ∟ Trisomy ∟ Diploidy \| ∟ Haploidy \| ∟ Polyploidy \| ∟ Chimerism \| ∟ Chromosomal Instability \| ∟ Chromosome Breakage \| ∟ Chromosome Deletion \| ∟ Inversion, Chromosome \| ∟ Isochromosomes \| ∟ Micronuclei, Chromosome-Defective \| ∟ Mosaicism \| ∟ Nondisjunction, Genetic \| ∟ Ring Chromosomes \| ∟ Sex Chromosome Aberrations \| ∟ Translocation, Genetic \| ∟ Uniparental Disomy Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Variation (Genetics) ∟ Mutation ∟ Chromosome Aberrations ∟ Aneuploidy 16 coordinate concepts 2 subordinate concepts ∟ Monosomy \| ∟ Trisomy ∟ Diploidy \| ∟ Haploidy \| ∟ Polyploidy \| ∟ Chimerism \| ∟ Chromosomal Instability \| ∟ Chromosome Breakage \| ∟ Chromosome Deletion \| ∟ Inversion, Chromosome \| ∟ Isochromosomes \| ∟ Micronuclei, Chromosome-Defective \| ∟ Mosaicism \| ∟ Nondisjunction, Genetic \| ∟ Ring Chromosomes \| ∟ Sex Chromosome Aberrations \| ∟ Translocation, Genetic \| ∟ Uniparental Disomy Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Pathologic Processes ∟ Chromosome Aberrations ∟ Aneuploidy 16 coordinate concepts 2 subordinate concepts ∟ Monosomy \| ∟ Trisomy ∟ Diploidy \| ∟ Haploidy \| ∟ Polyploidy \| ∟ Chimerism \| ∟ Chromosomal Instability \| ∟ Chromosome Breakage \| ∟ Chromosome Deletion \| ∟ Inversion, Chromosome \| ∟ Isochromosomes \| ∟ Micronuclei, Chromosome-Defective \| ∟ Mosaicism \| ∟ Nondisjunction, Genetic \| ∟ Ring Chromosomes \| ∟ Sex Chromosome Aberrations \| ∟ Translocation, Genetic \| ∟ Uniparental Disomy X
Broader terms:	Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Ploidies ∟ Aneuploidy Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Variation (Genetics) ∟ Mutation ∟ Chromosome Aberrations ∟ Aneuploidy Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Pathologic Processes ∟ Chromosome Aberrations ∟ Aneuploidy Ploidies > Genetic Phenomena > Medical Subject Headings (MeSH) Chromosome Aberrations > Mutation > Variation (Genetics) > Genetic Phenomena > Medical Subject Headings (MeSH) Chromosome Aberrations > Pathologic Processes > Pathological Conditions, Signs and Symptoms > Medical Subject Headings (MeSH) X
Narrower terms:	Monosomy \| Trisomy X
History note:	Chromosome Abnormalities (1966-1967)X
historyNote*:	68 X
publicMeSHNote*:	68 X
Scope note:	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). X
activeMeSHYear*:	2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1968-01-01X
dateRevised*:	2003-07-09X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Diploidy \| Haploidy \| Polyploidy \| Chimerism \| Chromosomal Instability \| Chromosome Breakage \| Chromosome Deletion \| Inversion, Chromosome \| Isochromosomes \| Micronuclei, Chromosome-Defective \| Mosaicism \| Nondisjunction, Genetic \| Ring Chromosomes \| Sex Chromosome Aberrations \| Translocation, Genetic \| Uniparental Disomy X
URI:	X
Labels and equivalent concepts:	Aneuploidia (fi) Aneuploidisuus (fi, replaced) Aneuploidi (sv) Aneuploid (en, replaced) X
Share:	X