Disease: Epilepsy, Rolandic ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		0.320 Biomarker disease BEFREE In conclusion our data do not support a major role of ELP4 and SRPX2 in the etiology of RE/ARE. 24995671 2014
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		0.320 GeneticVariation disease BEFREE Mutations in SRPX2 (Sushi-Repeat Protein, X-linked 2) cause rolandic epilepsy with speech impairment (RESDX syndrome) or with altered development of the speech cortex (bilateral perisylvian polymicrogyria). 18718938 2008
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		0.320 GeneticVariation disease ORPHANET