Disease: Seizures ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0036572
Disease: Seizures
Seizures 		0.130 GeneticVariation phenotype BEFREE (Ile589Thr) heterozygous mutation in the ATP1A2 gene in a Saudi kindred with hemiplegic attacks and seizures. 24097848 2014
CUI: C0036572
Disease: Seizures
Seizures 		0.130 Biomarker phenotype BEFREE The ATP1A2 gene does not appear to be involved in the ethiopathogenesis of pure BFIC syndromes, at least in the explored Italian multiplex families. 16026932 2005
CUI: C0036572
Disease: Seizures
Seizures 		0.130 Biomarker phenotype LHGDN Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants. 15159495 2004
CUI: C0036572
Disease: Seizures
Seizures 		0.130 Biomarker phenotype HPO