Disease: MIGRAINE, SPORADIC HEMIPLEGIC ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC 		0.180 GeneticVariation disease BEFREE Subsequent genetic analysis revealed the T666M mutation in the CACNA1A gene of chromosome 19.He was diagnosed with SHM. 24270521 2014
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC 		0.180 GeneticVariation disease BEFREE The heterogeneous spectrum of CACNA1A gene mutations probably causes sporadic hemiplegic migraine (SHM) to be misdiagnosed. 22527033 2012
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC 		0.180 Biomarker disease BEFREE Diagnostic screening of FHM genes in SHM patients can be of value. 20974584 2011
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC 		0.180 GeneticVariation disease BEFREE Sporadic hemiplegic migraine and epilepsy associated with CACNA1A gene mutation. 20071244 2010
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC 		0.180 GeneticVariation disease BEFREE De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine. 20837964 2010
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC 		0.180 GeneticVariation disease BEFREE Only very few DNA variants were identified in 100 SHM patients, and regardless of whether the identified variants are causal the CACNA1A and ATP1A2 genes are not major genes in SHM. 18513263 2008
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC 		0.180 GeneticVariation disease BEFREE We conclude that the Serine-218-Leucine mutation in the calcium channel, voltage-dependent, P/Q type, alpha-1A subunit gene is involved in sporadic hemiplegic migraine, delayed cerebral edema and coma after minor head trauma. 16638514 2006
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC 		0.180 Biomarker disease BEFREE To investigate the involvement of the CACNA1A calcium channel subunit gene in SHM. 12056940 2002
CUI: C1832903
Disease: MIGRAINE, SPORADIC HEMIPLEGIC
MIGRAINE, SPORADIC HEMIPLEGIC 		0.180 CausalMutation disease CLINVAR