ONKI3 | MedIEQ: Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Suppression, Genetic

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Variation (Genetics) ∟ Mutation ∟ Suppression, Genetic 18 coordinate concepts ∟ DNA Repeat Expansion \| ∟ Gene Amplification \| ∟ Gene Duplication \| ∟ Inversion, Chromosome \| ∟ Mutagenesis, Insertional \| ∟ Nondisjunction, Genetic \| ∟ Sequence Deletion \| ∟ Somatic Hypermutation, Immunoglobulin \| ∟ Translocation, Genetic \| ∟ Allelic Imbalance \| ∟ Base Pair Mismatch \| ∟ Chromosome Aberrations \| ∟ Codon, Nonsense \| ∟ Frameshift Mutation \| ∟ Genomic Instability \| ∟ Germ-Line Mutation \| ∟ Mutation, Missense \| ∟ Point Mutation Medical Subject Headings (MeSH) ∟ Genetic Processes ∟ Mutagenesis ∟ Suppression, Genetic 18 coordinate concepts ∟ DNA Repeat Expansion \| ∟ Gene Amplification \| ∟ Gene Duplication \| ∟ Inversion, Chromosome \| ∟ Mutagenesis, Insertional \| ∟ Nondisjunction, Genetic \| ∟ Sequence Deletion \| ∟ Somatic Hypermutation, Immunoglobulin \| ∟ Translocation, Genetic \| ∟ Allelic Imbalance \| ∟ Base Pair Mismatch \| ∟ Chromosome Aberrations \| ∟ Codon, Nonsense \| ∟ Frameshift Mutation \| ∟ Genomic Instability \| ∟ Germ-Line Mutation \| ∟ Mutation, Missense \| ∟ Point Mutation X
Broader terms:	Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Variation (Genetics) ∟ Mutation ∟ Suppression, Genetic Medical Subject Headings (MeSH) ∟ Genetic Processes ∟ Mutagenesis ∟ Suppression, Genetic Mutation > Variation (Genetics) > Genetic Phenomena > Medical Subject Headings (MeSH) Mutagenesis > Genetic Processes > Medical Subject Headings (MeSH) X
History note:	Genes (1966-1967) \| Genes, Suppressor (1968-1979)X
historyNote*:	80; was GENES, SUPPRESSOR 1968-79 (Prov 1968-69) X
publicMeSHNote*:	80; was GENES, SUPPRESSOR 1970-79 X
Scope note:	Mutation process that restores the wild-type PHENOTYPE in an organism possessing a mutationally altered GENOTYPE. The second "suppressor" mutation may be on a different gene, on the same gene but located at a distance from the site of the primary mutation, or in extrachromosomal genes (EXTRACHROMOSOMAL INHERITANCE). X
activeMeSHYear*:	2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1970-01-01X
dateRevised*:	2002-07-03X
recordAuthorizer*:	sjnX
recordMaintainer*:	TPWX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	DNA Repeat Expansion \| Gene Amplification \| Gene Duplication \| Inversion, Chromosome \| Mutagenesis, Insertional \| Nondisjunction, Genetic \| Sequence Deletion \| Somatic Hypermutation, Immunoglobulin \| Translocation, Genetic \| Allelic Imbalance \| Base Pair Mismatch \| Chromosome Aberrations \| Codon, Nonsense \| Frameshift Mutation \| Genomic Instability \| Germ-Line Mutation \| Mutation, Missense \| Point Mutation X
URI:	X
Labels and equivalent concepts:	Geneettinen suppressio (fi) Genetic Suppression (en, replaced) Supresión Genética (es) γενετική καταστολή (el) Suppression, genetische (de) suprese genetická (cs) Mutación de Supresores (es, replaced) Suppressor-Mutation (de, replaced) X
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