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Summary Literature (4)
DOID:891 - progressive myoclonus epilepsy

Disease Ontology Definition:A variable age at onset electroclinical syndrome characterized by a relentlessly progressive disease course until death.

Synonyms: PME, progressive Myoclonus epilepsy, progressive myoclonic epilepsy, progressive myoclonic epilepsy (disorder), progressive myoclonic epilepsy (disorder) [Ambiguous],

Xenbase Genes : prickle1, lmnb2, scarb2, epm2a, prdm8, kctd7, cstb, cers1, kcnc1, nhlrc1, gosr2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0020074 - progressive myoclonus epilepsy


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): variable age at onset electroclinical syndrome (is_a)