Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0338488
Disease: Alternating hemiplegia of childhood
Alternating hemiplegia of childhood
0.310 GeneticVariation disease ORPHANET These results also suggest that CACNA1A mutation scanning is indicated in patients with a severe neurological phenotype that includes paroxysmal (alternating) hemiplegia. 18498393 2008
CUI: C0338488
Disease: Alternating hemiplegia of childhood
Alternating hemiplegia of childhood
0.310 GeneticVariation disease BEFREE These results also suggest that CACNA1A mutation scanning is indicated in patients with a severe neurological phenotype that includes paroxysmal (alternating) hemiplegia. 18498393 2008