FLNC, filamin C, 2318

N. diseases: 132; N. variants: 56
Disease: Familial (FPAH) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 GeneticVariation disease BEFREE A novel familial truncating mutation in the filamin C gene associated with cardiac arrhythmias. 30118858 2019