Unverricht-Lundborg syndrome

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Summary

Literature (0)

DOID:3535 - Unverricht-Lundborg syndrome

Disease Ontology Definition:A progressive myoclonus epilepsy characterized by onset between 6 and 13 years of age of action- and stimulus-sensitive myoclonus, tonic-clonic seizures with ataxia, and a mild cognitive decline.

Synonyms: Unverricht - Lundborg disease, Unverricht's disease, Unverricht-Lundborg disease

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

MIM:

MIM:254800 - myoclonic epilepsy of unverricht and lundborg

MIM:254800 - myoclonic epilepsy of unverricht and lundborg

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): progressive myoclonus epilepsy (is_a)