FLNC, filamin C, 2318

N. diseases: 132; N. variants: 56
Disease: Cardiomyopathy, Hypertrophic, Familial ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
Cardiomyopathy, Hypertrophic, Familial 		0.110 GeneticVariation disease BEFREE Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy. 25351925 2014
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
Cardiomyopathy, Hypertrophic, Familial 		0.110 GeneticVariation disease CLINVAR