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Cardiovascular Diseases: all > Cardiovascular Diseases [MESH:D002318] > Heart Diseases [MESH:D006331] > Cardiomyopathies [MESH:D009202] > Cardiomyopathy, Hypertrophic [MESH:D002312] Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of [MESH:C567006] (27) Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency [MESH:C565784] (11) Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339) Deafness, Sensorineural, with Hypertrophic Cardiomyopathy [MESH:C565236] (1) Lipoatrophy with diabetes, hepatic steatosis, cardiomyopathy, and leukomelanodermic papules [MESH:C535905] (1) C15. Hemic and Lymphatic Diseases (group results) Hematologic Diseases [MESH:D006402] (1341) Lymphatic Diseases [MESH:D008206] (1368) Z. Exceptions (308) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities (group results) Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (1495) Z. Exceptions (4) C17. 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These terms define your current search. Click the × to remove a term. C14. Cardiovascular Diseases: Cardiovascular Diseases [MESH:D002318] > Heart Diseases [MESH:D006331] > Cardiomyopathies [MESH:D009202] > Cardiomyopathy, Hypertrophic [MESH:D002312] × 1516 items, grouped by C14. Cardiovascular Diseases (view ungrouped items) Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of [MESH:C567006] (27)    MESH:C006253   pirinixic acid C006253               MESH:C009505   4,4'-diaminodiphenylmethane C009505               MESH:C018021   cobaltous chloride C018021               MESH:C089730   rosiglitazone C089730               MESH:C482199   lipopolysaccharide, E coli O55-B5 C482199               MESH:C558013   NSC 689534 C558013               all 27 items... Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency [MESH:C565784] (11)    MESH:C517041   (4-amino-1,4-dihydro-3-(2-pyridyl)-5-thioxo-1,2,4-triazole)copper(II) C517041               MESH:C532162   2-(1H-indazol-4-yl)-6-(4-methanesulfonylpiperazin-1-ylmethyl)-4-morpholin-4 -ylthieno(3,2-d)pyrimidine C532162               MESH:C565784   Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency C565784               MESH:D001564   Benzo(a)pyrene D001564               MESH:D003300   Copper D003300               MESH:D006861   Hydrogen Peroxide D006861               all 11 items... Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)    MESH:C002741   N-nitrosomorpholine C002741               MESH:C003853   carboxyatractyloside C003853               MESH:C005219   methyl cellosolve C005219               MESH:C005274   naringin C005274               MESH:C006253   pirinixic acid C006253               MESH:C006632   arsenic trioxide C006632               all 339 items... Deafness, Sensorineural, with Hypertrophic Cardiomyopathy [MESH:C565236] (1)    MESH:C565236   Deafness, Sensorineural, with Hypertrophic Cardiomyopathy C565236               Lipoatrophy with diabetes, hepatic steatosis, cardiomyopathy, and leukomelanodermic papules [MESH:C535905] (1)    MESH:C535905   Lipoatrophy with diabetes, hepatic steatosis, cardiomyopathy, and leukomelanodermic papules C535905                (others) (1163)    MESH:C000188   alachlor C000188               MESH:C000474   cholestane-3,5,6-triol C000474               MESH:C001277   geldanamycin C001277               MESH:C001758   bendamustine C001758               MESH:C001803   tempol C001803               MESH:C002029   17alpha-ethynylestr-5(10)-ene-3alpha,17beta-diol C002029               all 1163 items...