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

Sequence Deletion

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Variation (Genetics) ∟ Mutation ∟ Sequence Deletion 18 coordinate concepts 2 subordinate concepts ∟ Chromosome Deletion \| ∟ Gene Deletion ∟ DNA Repeat Expansion \| ∟ Gene Amplification \| ∟ Gene Duplication \| ∟ Inversion, Chromosome \| ∟ Mutagenesis, Insertional \| ∟ Nondisjunction, Genetic \| ∟ Somatic Hypermutation, Immunoglobulin \| ∟ Suppression, Genetic \| ∟ 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 ∟ Sequence Deletion 18 coordinate concepts 2 subordinate concepts ∟ Chromosome Deletion \| ∟ Gene Deletion ∟ DNA Repeat Expansion \| ∟ Gene Amplification \| ∟ Gene Duplication \| ∟ Inversion, Chromosome \| ∟ Mutagenesis, Insertional \| ∟ Nondisjunction, Genetic \| ∟ Somatic Hypermutation, Immunoglobulin \| ∟ Suppression, Genetic \| ∟ 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 ∟ Sequence Deletion Medical Subject Headings (MeSH) ∟ Genetic Processes ∟ Mutagenesis ∟ Sequence Deletion Mutation > Variation (Genetics) > Genetic Phenomena > Medical Subject Headings (MeSH) Mutagenesis > Genetic Processes > Medical Subject Headings (MeSH) X
Narrower terms:	Chromosome Deletion \| Gene Deletion X
Annotation:	coord IM with BASE SEQUENCE or AMINO ACID SEQUENCE (IM); DF: SEQ DELETION X
History note:	Mutation (1976-1992)X
historyNote*:	93 X
publicMeSHNote*:	93 X
Scope note:	Deletion of sequences of nucleic acids from the genetic material of an individual. X
activeMeSHYear*:	2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1992-05-22X
dateEstablished*:	1993-01-01X
dateRevised*:	2002-07-03X
recordAuthorizer*:	sjnX
recordMaintainer*:	PXPX
recordOriginator*:	PXPX
Type:	Concept X
Coordinate terms:	DNA Repeat Expansion \| Gene Amplification \| Gene Duplication \| Inversion, Chromosome \| Mutagenesis, Insertional \| Nondisjunction, Genetic \| Somatic Hypermutation, Immunoglobulin \| Suppression, Genetic \| 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:	Sekvenssin deleetio (fi) Eliminación de Secuencia (es) απάλειψη αλληλουχίας (el) Sequenzdeletion (de) sekvence - ztráta (cs) Sequenztilgung (de, replaced) Sequenzlöschung (de, replaced) X
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