Monarch Disease Ontology id MONDO_0014883 (hypertrophic cardiomyopathy 26) is any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the FLNC gene. Also known as: CMH26, FLNC hypertrophic cardiomyopathy, cardiomyopathy familial hypertrophic 26, cardiomyopathy, familial hypertrophic, 26, cardiomyopathy, familial hypertrophic, type 26, cardiomyopathy, familial restrictive 5, hypertrophic cardiomyopathy caused by mutation in FLNC, hypertrophic cardiomyopathy type 26.