LMNB2, lamin B2, 84823

N. diseases: 74; N. variants: 3
Disease: Myoclonic Epilepsies, Progressive ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0751778
Disease: Myoclonic Epilepsies, Progressive
Myoclonic Epilepsies, Progressive 		0.310 GeneticVariation disease BEFREE Mutation of the nuclear lamin gene LMNB2 in progressive myoclonus epilepsy with early ataxia. 25954030 2015
CUI: C0751778
Disease: Myoclonic Epilepsies, Progressive
Myoclonic Epilepsies, Progressive 		0.310 Biomarker disease CTD_human