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Hypertrophic Cardiomyopathy
Informaţii despre
Nume
Hypertrophic Cardiomyopathy
Pagina Web
www.malacards.org
Clasificare globală Malacards
Boli genetice
;
Boli rare
Clasificari ICD10
Obstructive hypertrophic cardiomyopathy
Clasificare anatomică Malacards
Boli cardiovasculare
Boli din aceeaşi familie
Cardiomyopathy, Familial Hypertrophic, 1
;
Cardiomyopathy, Familial Hypertrophic, 10
;
Cardiomyopathy, Familial Hypertrophic, 11
;
Cardiomyopathy, Familial Hypertrophic, 12
;
Cardiomyopathy, Familial Hypertrophic, 13
;
Cardiomyopathy, Familial Hypertrophic, 14
;
Cardiomyopathy, Familial Hypertrophic, 15
;
Cardiomyopathy, Familial Hypertrophic, 16
;
Cardiomyopathy, Familial Hypertrophic, 17
;
Cardiomyopathy, Familial Hypertrophic, 18
;
Cardiomyopathy, Familial Hypertrophic, 19
;
Cardiomyopathy, Familial Hypertrophic, 2
;
Cardiomyopathy, Familial Hypertrophic, 20
;
Cardiomyopathy, Familial Hypertrophic, 21
;
Cardiomyopathy, Familial Hypertrophic, 25
;
Cardiomyopathy, Familial Hypertrophic, 26
;
Cardiomyopathy, Familial Hypertrophic, 3
;
Cardiomyopathy, Familial Hypertrophic, 4
;
Cardiomyopathy, Familial Hypertrophic, 6
;
Cardiomyopathy, Familial Hypertrophic, 7
;
Cardiomyopathy, Familial Hypertrophic, 8
;
Cardiomyopathy, Familial Hypertrophic, 9
;
Cardiomyopathy, Infantile Hypertrophic
;
Hypertrophic Cardiomyopathy Due to Intensive Athletic Training
Vezi şi
Boli A-Z
3-Methylglutaconic Aciduria
Accessory Mitral Valve Tissue
Achalasia
Acquired Metabolic Disease
Acrocallosal Syndrome
Acrofacial Dysostosis
Acute Myocardial Infarction
Acute Myocarditis
Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of
Adenocarcinoma
Adie Pupil
Aging
Alcoholic Cardiomyopathy
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome
Alport Syndrome, X-Linked
Al-Raqad Syndrome
Amyloidosis
Androgen Insensitivity Syndrome, Mild
Aneurysm
Angina Pectoris
Aniridia 1
Anorexia Nervosa 1
Aromatic Alpha-Keto Acid Reductase
Arrhythmogenic Right Ventricular Cardiomyopathy
Arteries, Anomalies of
Arteriovenous Fistula
Arthrochalasia Ehlers-Danlos Syndrome
Ataxia and Polyneuropathy, Adult-Onset
Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus
Ataxia Neuropathy Spectrum
Atrial Fibrillation
Atrial Standstill 1
Atrial Tachyarrhythmia with Short Pr Interval
Atrioventricular Block
Atrioventricular Septal Defect
Beckwith-Wiedemann Syndrome
Bleeding Disorder, Platelet-Type, 11
Blood Group--Ahonen
Blood Group, Dombrock System
Blood Group, I System
Body Mass Index Quantitative Trait Locus 10
Body Mass Index Quantitative Trait Locus 11
Body Mass Index Quantitative Trait Locus 12
Body Mass Index Quantitative Trait Locus 14
Body Mass Index Quantitative Trait Locus 18
Body Mass Index Quantitative Trait Locus 4
Body Mass Index Quantitative Trait Locus 7
Body Mass Index Quantitative Trait Locus 8
Body Mass Index Quantitative Trait Locus 9
Bohring-Opitz Syndrome
Bornholm Eye Disease
Brugada Syndrome
Burns
Cardiac Arrest
Cardiac Conduction Defect
Cardiac Rupture
Cardiac Sarcoidosis
Cardiac Tamponade
Cardioencephalomyopathy
Cardiofaciocutaneous Syndrome 1
Cardiogenic Shock
Cardiomyopathy, Dilated, 1e
Cardiomyopathy, Familial Hypertrophic, 1
Cardiomyopathy, Familial Hypertrophic, 21
Cardiomyopathy, Familial Hypertrophic, 4
Cardiomyopathy, Familial Hypertrophic, 6
Cardiomyopathy, Infantile Hypertrophic
Cardioneuromyopathy with Hyaline Masses and Nemaline Rods
Cataract
Central Core Disease of Muscle
Chagas Disease
Chromosomal Triplication
Chronic Fatigue Syndrome
Combined Oxidative Phosphorylation Deficiency 9
Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy
Complete Atrioventricular Canal
Congenital Cataract-Hypertrophic Cardiomyopathy-Mitochondrial Myopathy Syndrome
Congenital Cytomegalovirus
Congenital Disorder of Glycosylation, Type Ia
Congestive Heart Failure
Constrictive Pericarditis
Cornelia De Lange Syndrome
Coronary Stenosis
Cor Triatriatum
Costello Syndrome
Cranioectodermal Dysplasia 1
Crouzon Syndrome
Crouzon Syndrome with Acanthosis Nigricans
Cytomegalovirus Infection
Cytoplasmic Body Myopathy
Danon Disease
Dextrocardia
Diabetes Mellitus
Diastolic Heart Failure
Diffuse Lymphatic Malformation
Dilated Cardiomyopathy
Disseminated Intravascular Coagulation
Donohue Syndrome
Down Syndrome
Dwarfism
Dysostosis
Ebstein Anomaly
Encephalomyopathy
Encephalopathy
Endocardial Fibroelastosis
Endocarditis
Endocrine-Cerebroosteodysplasia
Endomyocardial Fibrosis
Endotheliitis
End Stage Renal Failure
Epilepsy
Extrinsic Cardiomyopathy
Fabry Disease
Facial Hemiatrophy
Factor Vii Deficiency
Factor X Deficiency
Fainting
Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form
Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form
Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form
Familial Isolated Dilated Cardiomyopathy
Familial Isolated Restrictive Cardiomyopathy
Fasciitis
Fatal Infantile Cytochrome C Oxidase Deficiency
Fatal Infantile Encephalocardiomyopathy
Fibroblastic Rheumatism
Fibromatosis
Fibromuscular Dysplasia
Gastric Adenocarcinoma
Gigantism
Gitelman Syndrome
Glycogen Storage Disease
Glycogen Storage Disease Ii
Glycogen Storage Disease, Type Ixd
Gonadal Dysgenesis
Heart Disease
Hemifacial Atrophy, Progressive
Hemopericardium
Hemophagocytic Lymphohistiocytosis, Familial, 1
Hemophagocytic Lymphohistiocytosis, Familial, 2
Hepatic Adenomas, Familial
Hepatitis
Hepatitis C
Hepatitis C Virus
Hereditary Spherocytosis
Hydrops, Lactic Acidosis, and Sideroblastic Anemia
Hypercholesterolemia, Autosomal Dominant, 3
Hypercholesterolemia, Familial
Hyperinsulinemic Hypoglycemia
Hyperinsulinemic Hypoglycemia, Familial, 3
Hyperinsulinemic Hypoglycemia, Familial, 4
Hyperinsulinism
Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy
Hypertensive Heart Disease
Hyperthyroidism
Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1
Hypoglycemia
Hypotonia
Hypoxia
Inclusion Body Myositis
Infective Endocarditis
Inferior Myocardial Infarction
Insulin-Like Growth Factor I
Interstitial Nephritis
Intrinsic Cardiomyopathy
Ischemia
Ischemic Heart Disease
Lactic Acidosis
Laryngeal Cleft
Laryngitis
Left Ventricular Noncompaction
Leiomyosarcoma
Lentigines
Leopard Syndrome
Limb-Girdle Muscular Dystrophy
Limb Ischemia
Lipodystrophy
Lissencephaly 1
Liver Cirrhosis
Loeffler Endocarditis
Long Qt Syndrome
Lymphoma
Macs Syndrome
Marfan Syndrome
Mitochondrial Disorders
Mitochondrial Encephalomyopathy
Mitochondrial Myopathy
Miyoshi Muscular Dystrophy 1
Morbid Obesity
Motor Neuron Disease
Mucolipidosis Ii Alpha/beta
Muscle Hypertrophy
Muscular Dystrophy
Muscular Dystrophy, Limb-Girdle, Type 2a
Muscular Dystrophy, Limb-Girdle, Type 2f
Mutism
Myocardial Infarction
Myocardial Stunning
Myocarditis
Myoclonus
Myopathy
Myopathy, Spheroid Body
Myosin Storage Myopathy
Myositis
Myotonic Dystrophy
Nemaline Myopathy
Nephrotic Syndrome
Neurofibromatosis-Noonan Syndrome
Neuronal Ceroid Lipofuscinosis
Neuronitis
Neutropenia
Noonan Syndrome 1
Noonan Syndrome with Multiple Lentigines
Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy
Ovarian Cyst
Pancreatitis
Parametritis
Pericardial Effusion
Pericarditis
Pheochromocytoma
Phosphorylase Kinase Deficiency
Platelet Glycoprotein Iv Deficiency
Posterior Urethral Valves
Progressive Familial Heart Block, Type Ib
Pulmonary Edema
Pulmonary Embolism
Pulmonary Hypertension
Pulmonary Interstitial Glycogenosis
Pulmonary Valve Stenosis
Pulmonary Vein Stenosis
Pulmonic Stenosis
Renal Glucosuria
Renal Hypodysplasia/aplasia 1
Restrictive Cardiomyopathy
Rheumatic Heart Disease
Right Bundle Branch Block
Rigid Spine Muscular Dystrophy 1
Sarcoidosis 2
Schnyder Corneal Dystrophy
Sengers Syndrome
Sensorineural Hearing Loss
Septal Myocardial Infarction
Short Qt Syndrome
Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities
Sick Sinus Syndrome
Sideroblastic Anemia
Siderosis
Situs Inversus
Sleep Apnea
Spasticity
Spinocerebellar Atrophy
Spiradenoma
Splenic Infarction
Spondyloocular Syndrome
Subacute Cerebellar Degeneration
Subaortic Stenosis, Membranous
Subendocardial Myocardial Infarction
Subpulmonary Stenosis
Subvalvular Aortic Stenosis
Syncope
Systolic Heart Failure
Tetralogy of Fallot
Three M Syndrome 1
Thrombocytopenia
Thrombosis
Tyrosinemia
Ventricular Septal Defect
Vitamin B12 Deficiency
Williams-Beuren Syndrome
Wolff-Parkinson-White Syndrome
Wolf-Hirschhorn Syndrome
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