ONKI3 | Medical Subject Headings

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Chromosome Deletion

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Variation (Genetics) ∟ Mutation ∟ Allelic Imbalance ∟ Loss of Heterozygosity ∟ Chromosome Deletion 14 coordinate concepts ∟ Gene Deletion \| ∟ Aneuploidy \| ∟ Chimerism \| ∟ Chromosomal Instability \| ∟ Chromosome Breakage \| ∟ 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 ∟ Chromosome Deletion 14 coordinate concepts ∟ Gene Deletion \| ∟ Aneuploidy \| ∟ Chimerism \| ∟ Chromosomal Instability \| ∟ Chromosome Breakage \| ∟ 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 ∟ Sequence Deletion ∟ Chromosome Deletion 14 coordinate concepts ∟ Gene Deletion \| ∟ Aneuploidy \| ∟ Chimerism \| ∟ Chromosomal Instability \| ∟ Chromosome Breakage \| ∟ Inversion, Chromosome \| ∟ Isochromosomes \| ∟ Micronuclei, Chromosome-Defective \| ∟ Mosaicism \| ∟ Nondisjunction, Genetic \| ∟ Ring Chromosomes \| ∟ Sex Chromosome Aberrations \| ∟ Translocation, Genetic \| ∟ Uniparental Disomy Medical Subject Headings (MeSH) ∟ Genetic Processes ∟ Mutagenesis ∟ Sequence Deletion ∟ Chromosome Deletion 14 coordinate concepts ∟ Gene Deletion \| ∟ Aneuploidy \| ∟ Chimerism \| ∟ Chromosomal Instability \| ∟ Chromosome Breakage \| ∟ 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 ∟ Chromosome Deletion 14 coordinate concepts ∟ Gene Deletion \| ∟ Aneuploidy \| ∟ Chimerism \| ∟ Chromosomal Instability \| ∟ Chromosome Breakage \| ∟ 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 ∟ Variation (Genetics) ∟ Mutation ∟ Allelic Imbalance ∟ Loss of Heterozygosity ∟ Chromosome Deletion Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Variation (Genetics) ∟ Mutation ∟ Chromosome Aberrations ∟ Chromosome Deletion Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Variation (Genetics) ∟ Mutation ∟ Sequence Deletion ∟ Chromosome Deletion Medical Subject Headings (MeSH) ∟ Genetic Processes ∟ Mutagenesis ∟ Sequence Deletion ∟ Chromosome Deletion Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Pathologic Processes ∟ Chromosome Aberrations ∟ Chromosome Deletion Loss of Heterozygosity > Allelic Imbalance > Mutation > Variation (Genetics) > Genetic Phenomena > Medical Subject Headings (MeSH) Chromosome Aberrations > Mutation > Variation (Genetics) > Genetic Phenomena > Medical Subject Headings (MeSH) Sequence Deletion > Mutation > Variation (Genetics) > Genetic Phenomena > Medical Subject Headings (MeSH) Sequence Deletion > Mutagenesis > Genetic Processes > Medical Subject Headings (MeSH) Chromosome Aberrations > Pathologic Processes > Pathological Conditions, Signs and Symptoms > Medical Subject Headings (MeSH) X
Annotation:	for coord see note on CHROMOSOME ABERRATIONS X
History note:	Chromosome Aberrations (1968-1974) \| Chromosome Abnormalities (1966-1967)X
historyNote*:	78(75); was see under CHROMOSOME ABERRATIONS 1975-77 X
publicMeSHNote*:	78; was see under CHROMOSOME ABERRATIONS 1975-77 X
Scope note:	Actual loss of a portion of the chromosome. X
activeMeSHYear*:	2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1974-11-11X
dateEstablished*:	1978-01-01X
dateRevised*:	2002-07-03X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	NLMX
Related term:	Gene Deletion X
Type:	Concept X
Coordinate terms:	Gene Deletion \| Aneuploidy \| Chimerism \| Chromosomal Instability \| Chromosome Breakage \| 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:	Kromosomideleetio (fi) Kromosomin deleetio (fi, replaced) Deleetio (fi, replaced) Kromosomdeletion (sv) Partial Monosomy (en, replaced) Monosomy, Partial (en, replaced) X
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