BC43.10
category
Familial-genetic hypertrophic cardiomyopathy
Definition
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.
Also indexed as
Familial hypertrophic cardiomyopathyFamilial-genetic hypertrophic cardiomyopathyFatty acid oxidation or ketogenesis disorder with hypertrophic cardiomyopathyGlycogen storage disease with hypertrophic cardiomyopathyHereditary ventricular hypertrophyHypertrophic cardiomyopathy due to AMP-activated protein kinase deficiencyHypertrophic cardiomyopathy due to Anderson–Fabry diseaseHypertrophic cardiomyopathy due to Beckwith–Wiedemann syndromeHypertrophic cardiomyopathy due to Carnitine-acylcarnitine translocase deficiencyHypertrophic cardiomyopathy due to Costello syndromeHypertrophic cardiomyopathy due to Donohue syndromeHypertrophic cardiomyopathy due to Friedreich's ataxiaHypertrophic cardiomyopathy due to Hurler diseaseHypertrophic cardiomyopathy due to Hurler disease (MPS I)Hypertrophic cardiomyopathy due to LAMP2 deficiency diseaseHypertrophic cardiomyopathy due to LEOPARD syndromeHypertrophic cardiomyopathy due to LeprechaunismHypertrophic cardiomyopathy due to MELASHypertrophic cardiomyopathy due to MELAS - [Mitochondrial Encephalopathy, Lactic acidosis, and Stroke-like episodes]Hypertrophic cardiomyopathy due to Noonan syndromeHypertrophic cardiomyopathy due to Noonan syndrome with multiple lentiginesHypertrophic cardiomyopathy due to PRKAG2 syndromeHypertrophic cardiomyopathy due to Pompe diseaseHypertrophic cardiomyopathy due to Swyer's syndromeHypertrophic cardiomyopathy due to carnitine deficiencyHypertrophic cardiomyopathy due to carnitine palmitoyl transferase II deficiencyHypertrophic cardiomyopathy due to craniofacialcutaneous syndromeHypertrophic cardiomyopathy due to disorder of fatty acid metabolismHypertrophic cardiomyopathy due to glycogen debranching enzyme deficiencyHypertrophic cardiomyopathy due to glycogen storage diseaseHypertrophic cardiomyopathy due to lysosomal storage diseaseHypertrophic cardiomyopathy due to mitochondrial disorderHypertrophic cardiomyopathy due to primary amyloidosisLysosomal disease with hypertrophic cardiomyopathyMitochondrial disease with hypertrophic cardiomyopathyOther specified familial diseases associated with hypertrophic cardiomyopathySarcomeric hypertrophic cardiomyopathySyndromic hypertrophic cardiomyopathy