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

Chromosome Fragility

Loading results...


Hierarchy:	Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Genomic Instability ∟ Chromosomal Instability ∟ Chromosome Fragility Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Variation (Genetics) ∟ Mutation ∟ Chromosome Aberrations ∟ Chromosomal Instability ∟ Chromosome Fragility Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Variation (Genetics) ∟ Mutation ∟ Genomic Instability ∟ Chromosomal Instability ∟ Chromosome Fragility Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Pathologic Processes ∟ Chromosome Aberrations ∟ Chromosomal Instability ∟ Chromosome Fragility Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Pathologic Processes ∟ Genomic Instability ∟ Chromosomal Instability ∟ Chromosome Fragility X
Broader terms:	Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Genomic Instability ∟ Chromosomal Instability ∟ Chromosome Fragility Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Variation (Genetics) ∟ Mutation ∟ Chromosome Aberrations ∟ Chromosomal Instability ∟ Chromosome Fragility Medical Subject Headings (MeSH) ∟ Genetic Phenomena ∟ Variation (Genetics) ∟ Mutation ∟ Genomic Instability ∟ Chromosomal Instability ∟ Chromosome Fragility Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Pathologic Processes ∟ Chromosome Aberrations ∟ Chromosomal Instability ∟ Chromosome Fragility Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Pathologic Processes ∟ Genomic Instability ∟ Chromosomal Instability ∟ Chromosome Fragility Chromosomal Instability > Genomic Instability > Genetic Phenomena > Medical Subject Headings (MeSH) Chromosomal Instability > Chromosome Aberrations > Mutation > Variation (Genetics) > Genetic Phenomena > Medical Subject Headings (MeSH) Chromosomal Instability > Genomic Instability > Mutation > Variation (Genetics) > Genetic Phenomena > Medical Subject Headings (MeSH) Chromosomal Instability > Chromosome Aberrations > Pathologic Processes > Pathological Conditions, Signs and Symptoms > Medical Subject Headings (MeSH) Chromosomal Instability > Genomic Instability > Pathologic Processes > Pathological Conditions, Signs and Symptoms > Medical Subject Headings (MeSH) X
History note:	Chromosome Aberrations (1968-1981) \| Chromosomes (1966-1967)X
historyNote*:	82 X
publicMeSHNote*:	82 X
Scope note:	Susceptibility of chromosomes to breakage leading to translocation; CHROMOSOME INVERSION; SEQUENCE DELETION; or other CHROMOSOME BREAKAGE related aberrations. X
activeMeSHYear*:	2004 \| 2005 \| 2006 \| 2006A \| 2006B \| 2007X
dateCreated*:	1981-02-23X
dateEstablished*:	1982-01-01X
dateRevised*:	2005-08-02X
recordAuthorizer*:	agsX
recordMaintainer*:	agsX
recordOriginator*:	AEPX
Related term:	Chromosome Breakage \| Chromosome Fragile Sites \| Fragile X Syndrome \| Trinucleotide Repeat Expansion X
Type:	Concept X
URI:	X
Labels and equivalent concepts:	Kromosomin hauraus (fi) Kromosomin fragiliteetti (fi, replaced) Kromosomsvaghet (sv) Chromosomal Fragility (en, replaced) X
Share:	X