FLNC, filamin C, 2318

N. diseases: 132; N. variants: 56
Disease: Familial cardiomyopathy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0264789
Disease: Familial cardiomyopathy
Familial cardiomyopathy 		0.010 Biomarker disease BEFREE All candidate genes but one (SLC39A8) exhibit preferential expression in striated muscle tissues and mutations in TTN, BAG3, FLNC and FHOD3 are known to cause familial cardiomyopathy. 28296976 2017