DISEASES Cardiovascular Diseases [C14] Cardiovascular Diseases Heart Diseases [C14.280] Heart Diseases Arrhythmias, Cardiac [C14.280.067] Arrhythmias, Cardiac Arrhythmia, Sinus [C14.280.067.093] Arrhythmia, Sinus Atrial Fibrillation [C14.280.067.198] Atrial Fibrillation Atrial Flutter [C14.280.067.248] Atrial Flutter Bradycardia [C14.280.067.319] Bradycardia Brugada Syndrome [C14.280.067.322] Brugada Syndrome Cardiac Complexes, Premature [C14.280.067.325] Cardiac Complexes, Premature Commotio Cordis [C14.280.067.441] Commotio Cordis Heart Block [C14.280.067.558] Heart Block Long QT Syndrome [C14.280.067.565] Long QT Syndrome Parasystole [C14.280.067.672] Parasystole Pre-Excitation Syndromes [C14.280.067.780] Pre-Excitation Syndromes Tachycardia [C14.280.067.845] Tachycardia Ventricular Fibrillation [C14.280.067.922] Ventricular Fibrillation Ventricular Flutter [C14.280.067.961] Ventricular Flutter DISEASES Cardiovascular Diseases [C14] Cardiovascular Diseases Heart Diseases [C14.280] Heart Diseases Cardiac Conduction System Disease [C14.280.123] Cardiac Conduction System Disease Brugada Syndrome [C14.280.123.250] Brugada Syndrome Cardiac Complexes, Premature [C14.280.123.375] Cardiac Complexes, Premature Heart Block [C14.280.123.500] Heart Block Long QT Syndrome [C14.280.123.625] Long QT Syndrome Pre-Excitation Syndromes [C14.280.123.750] Pre-Excitation Syndromes Tachycardia [C14.280.123.875] Tachycardia 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 Imprinting Disorders [C16.320.447] Imprinting Disorders 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

Brugada Syndrome - Conceito preferido

Identificador do conceito	M0496826
Nota de escopo	An autosomal dominant defect of cardiac conduction that is characterized by an abnormal ST-segment in leads V1-V3 on the ELECTROCARDIOGRAM resembling a right BUNDLE-BRANCH BLOCK; high risk of VENTRICULAR TACHYCARDIA; or VENTRICULAR FIBRILLATION; SYNCOPAL EPISODE; and possible sudden death. This syndrome is linked to mutations of gene encoding the cardiac SODIUM CHANNEL alpha subunit.
Termo preferido	Brugada Syndrome
Termo(s) alternativo(s)	Right Bundle Branch Block, ST Segment Elevation, and Sudden Death Syndrome Sudden Unexplained Death Syndrome Sudden Unexplained Nocturnal Death Syndrome Sudden Unexplained Nocturnal Death Syndrome (SUNDS)

Brugada ECG Pattern - Relacionado, mas não mais amplo ou mais específico

Identificador do conceito	M0496827
Termo preferido	Brugada ECG Pattern
Termo(s) alternativo(s)	Brugada Type ECG Pattern ECG Pattern, Brugada

Brugada Syndrome 1 - Mais específico

Identificador do conceito	M000648999
Termo preferido	Brugada Syndrome 1