BC43.10
Familial-genetic hypertrophic cardiomyopathy
Cardiomiopatia hipertrófica genética familiar
CategoryDefinition
Familial isolated hypertrophic cardiomyopathy is the presence of non-syndromic hypertrophic cardiomyopathy in multiple members of a pedigree, or in the presence of a genetic mutation known to be significantly associated with hypertrophic cardiomyopathy.
Index Terms
Familial-genetic hypertrophic cardiomyopathyFamilial hypertrophic cardiomyopathyHereditary ventricular hypertrophyHypertrophic cardiomyopathy due to disorder of fatty acid metabolismFatty acid oxidation or ketogenesis disorder with hypertrophic cardiomyopathyHypertrophic cardiomyopathy due to carnitine palmitoyl transferase II deficiencyHypertrophic cardiomyopathy due to Carnitine-acylcarnitine translocase deficiencyHypertrophic cardiomyopathy due to carnitine deficiencyHypertrophic cardiomyopathy due to glycogen storage diseaseGlycogen storage disease with hypertrophic cardiomyopathyHypertrophic cardiomyopathy due to AMP-activated protein kinase deficiencyHypertrophic cardiomyopathy due to PRKAG2 syndromeHypertrophic cardiomyopathy due to Pompe diseaseHypertrophic cardiomyopathy due to glycogen debranching enzyme deficiencyHypertrophic cardiomyopathy due to LAMP2 deficiency diseaseHypertrophic cardiomyopathy due to lysosomal storage diseaseLysosomal disease with hypertrophic cardiomyopathyHypertrophic cardiomyopathy due to Anderson–Fabry diseaseHypertrophic cardiomyopathy due to Hurler diseaseHypertrophic cardiomyopathy due to Hurler disease (MPS I)Hypertrophic cardiomyopathy due to mitochondrial disorderMitochondrial disease with hypertrophic cardiomyopathyHypertrophic cardiomyopathy due to MELASHypertrophic cardiomyopathy due to MELAS - [Mitochondrial Encephalopathy, Lactic acidosis, and Stroke-like episodes]Hypertrophic cardiomyopathy due to Friedreich's ataxiaOther specified familial diseases associated with hypertrophic cardiomyopathyHypertrophic cardiomyopathy due to primary amyloidosisSarcomeric hypertrophic cardiomyopathySyndromic hypertrophic cardiomyopathyHypertrophic cardiomyopathy due to craniofacialcutaneous syndromeHypertrophic cardiomyopathy due to Noonan syndromeHypertrophic cardiomyopathy due to Noonan syndrome with multiple lentiginesHypertrophic cardiomyopathy due to LEOPARD syndromeHypertrophic cardiomyopathy due to Costello syndromeHypertrophic cardiomyopathy due to Beckwith–Wiedemann syndromeHypertrophic cardiomyopathy due to Swyer's syndromeHypertrophic cardiomyopathy due to LeprechaunismHypertrophic cardiomyopathy due to Donohue syndrome