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

Myoclonic Epilepsies, Progressive

Loading results...


Hierarchy:	Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Epilepsy ∟ Epilepsies, Myoclonic ∟ Myoclonic Epilepsies, Progressive 1 coordinate concept 3 subordinate concepts ∟ Lafora Disease \| ∟ MERRF Syndrome \| ∟ Unverricht-Lundborg Syndrome ∟ Myoclonic Epilepsy, Juvenile X
Broader terms:	Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Epilepsy ∟ Epilepsies, Myoclonic ∟ Myoclonic Epilepsies, Progressive Epilepsies, Myoclonic > Epilepsy > Brain Diseases > Central Nervous System Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Lafora Disease \| MERRF Syndrome \| Unverricht-Lundborg Syndrome X
History note:	Epilepsies, Myoclonic (1977-1999) \| Epilepsy (1965-1999) \| Myoclonus (1968-1999)X
historyNote*:	2000; use Epilepsy, Myoclonic 1977-1999 X
publicMeSHNote*:	2000; see Epilepsy, Myoclonic 1977-1999 X
Scope note:	A heterogeneous group of primarily familial disorders characterized by myoclonic seizures, tonic-clonic seizures, ataxia, progressive intellectual deterioration, and neuronal degeneration. These include LAFORA DISEASE; MERRF SYNDROME; NEURONAL CEROID-LIPOFUSCINOSIS; sialidosis (see MUCOLIPIDOSES), and UNVERRICHT-LUNDBORG SYNDROME. X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-11-04X
dateEstablished*:	2000-01-01X
dateRevised*:	2001-07-25X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	KEVX
Type:	Concept X
Coordinate terms:	Myoclonic Epilepsy, Juvenile X
URI:	X
Labels and equivalent concepts:	Etenevät myoklonusepilepsiat (fi) Progressiiviset myoklonusepilepsiat (fi, replaced) Progressiivinen myoklonusepilepsia (fi, replaced) Progredioivat myoklonusepilepsiat (fi, replaced) Progredioiva myoklonusepilepsia (fi, replaced) Epilepsia, myoklonus-, etenevä (fi, replaced) Etenevä myoklonusepilepsia (fi, replaced) PME (fi, replaced) Myoklon epilepsi, progressiv (sv) May-Whites syndrom (sv, replaced) Progressive myoklon epilepsi (sv, replaced) Progressive Myoclonus Epilepsies (en, replaced) Progressive Myoclonic Epilepsy (en, replaced) Epilepsia myoclonica progressiva (la-FI, replaced) X
Share:	X