ONKI3 | Medical Subject Headings

The ONKI is provided as a part of the ONKI Living Lab - an open lab for testing the latest semantic web technologies in practice, with real users like you. Currently, over 10 000 people are using ONKI each month.

We hope you like the ONKI service and enjoy using it for your purposes!

If you encounter any problems or have improvement ideas, please contact the ONKI team. We are also very much interested in your success stories in using ONKI - please share your experiences!

The ONKI Team

Jouni Tuominen, Living Lab contact person, APIs, widgets, publishing of ontologies, etc.
Eero Hyvönen, professor, head of research group

Former members: Kim Viljanen, Rami Alatalo.

Building the future of the Semantic Web and beyond.

SeCo's homepage
For the latest semantic news, follow us on Twitter and fan us on Facebook!

How can we help you?

Live presentations about ONKI: what it is? how to use it?
Support for creating and publishing ontologies.
Online technical support for using ONKI.
Co-operation in projects.
And more, please ask.

suomeksi på svenska in English

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

The way concept relations are shown: separately in hierarchy

Sequence Deletion

Loading results...


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) Jakson deleetio (fi, replaced) Sekvensdeletion (sv) X
Share:	X