DISEASES Cardiovascular Diseases [C14] Cardiovascular Diseases Heart Diseases [C14.280] Heart Diseases Cardiomyopathies [C14.280.238] Cardiomyopathies Cardiomyopathy, Hypertrophic [C14.280.238.100] Cardiomyopathy, Hypertrophic Apical Hypertrophic Cardiomyopathy [C14.280.238.100.250] Apical Hypertrophic Cardiomyopathy Cardiomyopathy, Hypertrophic, Familial [C14.280.238.100.500] Cardiomyopathy, Hypertrophic, Familial DISEASES Cardiovascular Diseases [C14] Cardiovascular Diseases Heart Diseases [C14.280] Heart Diseases Heart Valve Diseases [C14.280.484] Heart Valve Diseases Aortic Valve Disease [C14.280.484.048] Aortic Valve Disease Aortic Valve Stenosis [C14.280.484.048.750] Aortic Valve Stenosis Aortic Stenosis, Subvalvular [C14.280.484.048.750.070] Aortic Stenosis, Subvalvular Cardiomyopathy, Hypertrophic [C14.280.484.048.750.070.160] Cardiomyopathy, Hypertrophic Cardiomyopathy, Hypertrophic, Familial [C14.280.484.048.750.070.160.500] Cardiomyopathy, Hypertrophic, Familial DISEASES Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] Congenital, Hereditary, and Neonatal Diseases and Abnormalities Genetic Diseases, Inborn [C16.320] Genetic Diseases, Inborn Adrenal Hyperplasia, Congenital [C16.320.033] Adrenal Hyperplasia, Congenital Alagille Syndrome [C16.320.051] Alagille Syndrome alpha 1-Antitrypsin Deficiency [C16.320.060] alpha 1-Antitrypsin Deficiency Anemia, Hemolytic, Congenital [C16.320.070] Anemia, Hemolytic, Congenital Anemia, Hypoplastic, Congenital [C16.320.077] Anemia, Hypoplastic, Congenital Ataxia Telangiectasia [C16.320.080] Ataxia Telangiectasia Autoimmune Lymphoproliferative Syndrome [C16.320.089] Autoimmune Lymphoproliferative Syndrome Blood Coagulation Disorders, Inherited [C16.320.099] Blood Coagulation Disorders, Inherited Brugada Syndrome [C16.320.100] Brugada Syndrome CADASIL [C16.320.129] CADASIL Camurati-Engelmann Syndrome [C16.320.144] Camurati-Engelmann Syndrome Cardiomyopathy, Hypertrophic, Familial [C16.320.160] Cardiomyopathy, Hypertrophic, Familial CHARGE Syndrome [C16.320.165] CHARGE Syndrome Cherubism [C16.320.170] Cherubism Chromosome Disorders [C16.320.180] Chromosome Disorders Ciliopathies [C16.320.184] Ciliopathies Costello Syndrome [C16.320.188] Costello Syndrome Cystic Fibrosis [C16.320.190] Cystic Fibrosis Donohue Syndrome [C16.320.215] Donohue Syndrome Dwarfism [C16.320.240] Dwarfism Eye Diseases, Hereditary [C16.320.290] Eye Diseases, Hereditary Familial Multiple Lipomatosis [C16.320.298] Familial Multiple Lipomatosis Frasier Syndrome [C16.320.306] Frasier Syndrome GATA2 Deficiency [C16.320.314] GATA2 Deficiency Genetic Diseases, X-Linked [C16.320.322] Genetic Diseases, X-Linked Genetic Diseases, Y-Linked [C16.320.338] Genetic Diseases, Y-Linked Hajdu-Cheney Syndrome [C16.320.355] Hajdu-Cheney Syndrome Hemoglobinopathies [C16.320.365] Hemoglobinopathies Hereditary Autoinflammatory Diseases [C16.320.382] Hereditary Autoinflammatory Diseases Heredodegenerative Disorders, Nervous System [C16.320.400] Heredodegenerative Disorders, Nervous System Hyper-IgM Immunodeficiency Syndrome [C16.320.413] Hyper-IgM Immunodeficiency Syndrome Hyperthyroxinemia, Familial Dysalbuminemic [C16.320.427] Hyperthyroxinemia, Familial Dysalbuminemic Kallmann Syndrome [C16.320.467] Kallmann Syndrome Kartagener Syndrome [C16.320.480] Kartagener Syndrome Laminopathies [C16.320.488] Laminopathies Lennox Gastaut Syndrome [C16.320.495] Lennox Gastaut Syndrome Loeys-Dietz Syndrome [C16.320.510] Loeys-Dietz Syndrome Marfan Syndrome [C16.320.540] Marfan Syndrome Metabolism, Inborn Errors [C16.320.565] Metabolism, Inborn Errors Muscular Dystrophies [C16.320.577] Muscular Dystrophies Myasthenic Syndromes, Congenital [C16.320.590] Myasthenic Syndromes, Congenital Nail-Patella Syndrome [C16.320.600] Nail-Patella Syndrome Neoplastic Syndromes, Hereditary [C16.320.700] Neoplastic Syndromes, Hereditary Oculocerebrorenal Syndrome [C16.320.709] Oculocerebrorenal Syndrome Orofaciodigital Syndromes [C16.320.714] Orofaciodigital Syndromes Osteoarthropathy, Primary Hypertrophic [C16.320.718] Osteoarthropathy, Primary Hypertrophic Osteochondrodysplasias [C16.320.728] Osteochondrodysplasias Osteogenesis Imperfecta [C16.320.737] Osteogenesis Imperfecta Pain Insensitivity, Congenital [C16.320.775] Pain Insensitivity, Congenital Pelger-Huet Anomaly [C16.320.784] Pelger-Huet Anomaly Primary Immunodeficiency Diseases [C16.320.798] Primary Immunodeficiency Diseases Pycnodysostosis [C16.320.812] Pycnodysostosis Renal Tubular Transport, Inborn Errors [C16.320.831] Renal Tubular Transport, Inborn Errors Skin Diseases, Genetic [C16.320.850] Skin Diseases, Genetic Werner Syndrome [C16.320.925] Werner Syndrome Yellow Nail Syndrome [C16.320.962] Yellow Nail Syndrome

Cardiomyopathy, Hypertrophic, Familial - Preferred

Concept UI	M0371730
Scope note	An autosomal dominant inherited form of HYPERTROPHIC CARDIOMYOPATHY. It results from any of more than 50 mutations involving genes encoding contractile proteins such as VENTRICULAR MYOSINS; cardiac TROPONIN T; ALPHA-TROPOMYOSIN.
Preferred term	Cardiomyopathy, Hypertrophic, Familial
Entry term(s)	Asymmetric Septal Hypertrophy, Familial Cardiomyopathies, Familial Hypertrophic Cardiomyopathy, Familial Hypertrophic Familial Hypertrophic Cardiomyopathies Familial Hypertrophic Cardiomyopathy Familial Ventricular Hypertrophies Familial Ventricular Hypertrophy Hereditary Ventricular Hypertrophies Hereditary Ventricular Hypertrophy Hypertrophic Cardiomyopathies, Familial Hypertrophic Cardiomyopathy, Familial Hypertrophies, Hereditary Ventricular Hypertrophy, Familial Ventricular Hypertrophy, Hereditary Ventricular Ventricular Hypertrophies, Familial Ventricular Hypertrophies, Hereditary Ventricular Hypertrophy, Familial Ventricular Hypertrophy, Hereditary

Obstructive Asymmetric Septal Hypertrophy - Related but not broader or narrower

Concept UI	M0579499
Preferred term	Obstructive Asymmetric Septal Hypertrophy

Hypertrophic Subaortic Stenosis, Idiopathic - Related but not broader or narrower

Concept UI	M0579500
Preferred term	Hypertrophic Subaortic Stenosis, Idiopathic