Disease: Tremor ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0040822
Disease: Tremor
Tremor 		0.110 GeneticVariation phenotype BEFREE Our study identified an Arg528His CACNL1A3 mutation in patients with hypoPP, and excluded this mutation as the cause of tremor or epilepsy in this kindred. 11034874 2000
CUI: C0040822
Disease: Tremor
Tremor 		0.110 Biomarker phenotype HPO