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Dilated Cardiomyopathy
Informaţii despre
Nume
Dilated Cardiomyopathy
Pagina Web
www.malacards.org
Clasificare globală Malacards
Boli genetice
;
Boli rare
Clasificari ICD10
Dilated cardiomyopathy
Clasificare anatomică Malacards
Boli ale urechii
;
Boli cardiovasculare
;
Boli neuronale
Boli din aceeaşi familie
Cardiomyopathy Due to Anthracyclines
;
Cardiomyopathy, Dilated, 1a
;
Cardiomyopathy, Dilated, 1b
;
Cardiomyopathy, Dilated, 1bb
;
Cardiomyopathy, Dilated, 1cc
;
Cardiomyopathy, Dilated, 1d
;
Cardiomyopathy, Dilated, 1dd
;
Cardiomyopathy, Dilated, 1e
;
Cardiomyopathy, Dilated, 1ee
;
Cardiomyopathy, Dilated, 1ff
;
Cardiomyopathy, Dilated, 1g
;
Cardiomyopathy, Dilated, 1gg
;
Cardiomyopathy, Dilated, 1h
;
Cardiomyopathy, Dilated, 1hh
;
Cardiomyopathy, Dilated, 1i
;
Cardiomyopathy, Dilated, 1ii
;
Cardiomyopathy, Dilated, 1j
;
Cardiomyopathy, Dilated, 1jj
;
Cardiomyopathy, Dilated, 1k
;
Cardiomyopathy, Dilated, 1kk
;
Cardiomyopathy, Dilated, 1l
;
Cardiomyopathy, Dilated, 1m
;
Cardiomyopathy, Dilated, 1nn
;
Cardiomyopathy, Dilated, 1o
;
Cardiomyopathy, Dilated, 1p
;
Cardiomyopathy, Dilated, 1q
;
Cardiomyopathy, Dilated, 1r
;
Cardiomyopathy, Dilated, 1u
;
Cardiomyopathy, Dilated, 1v
;
Cardiomyopathy, Dilated, 1w
;
Cardiomyopathy, Dilated, 1x
;
Cardiomyopathy, Dilated, 1z
;
Cardiomyopathy, Dilated, 2a
;
Cardiomyopathy, Dilated, 2b
;
Cardiomyopathy, Dilated, 3b
;
Dilated Cardiomyopathy 1t
Vezi şi
Boli A-Z
3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency
3-Hydroxyacyl-Coa Dehydrogenase Deficiency
3-Methylglutaconic Aciduria
3-Methylglutaconic Aciduria, Type V
Acquired Immunodeficiency Syndrome
Acquired Metabolic Disease
Acrocallosal Syndrome
Acrokeratosis Verruciformis
Acromegaly
Acute Mountain Sickness
Acute Myocardial Infarction
Acute Myocarditis
Acute Pyelonephritis
Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of
Adams-Oliver Syndrome
Adie Pupil
Adult-Onset Still's Disease
Aggressive Periodontitis
Aging
Al Amyloidosis
Allergic Contact Dermatitis
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome
Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity
Alport Syndrome, X-Linked
Al-Raqad Syndrome
Alzheimer Disease 3
Amyloidosis
Anauxetic Dysplasia 1
Andersen Cardiodysrhythmic Periodic Paralysis
Androgen Insensitivity Syndrome, Mild
Aneurysm
Angina Pectoris
Aniridia 1
Anorexia Nervosa 1
Anterolateral Myocardial Infarction
Antiphospholipid Syndrome
Anuria
Aortic Coarctation
Aortic Disease
Aortic Valve Disease 2
Apert Syndrome
Aphthous Stomatitis
Apnea, Obstructive Sleep
Appendicitis
Apraxia
Arrhythmogenic Right Ventricular Cardiomyopathy
Arrhythmogenic Right Ventricular Dysplasia, Familial, 5
Arrhythmogenic Right Ventricular Dysplasia, Familial, 8
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9
Arteries, Anomalies of
Arthritis
Arthrochalasia Ehlers-Danlos Syndrome
Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect
Aseptic Meningitis
Ataxia and Polyneuropathy, Adult-Onset
Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus
Ataxia Neuropathy Spectrum
Atrial Fibrillation
Atrial Heart Septal Defect
Atrial Septal Aneurysm
Atrial Septal Defect 4
Atrial Standstill
Atrial Standstill 1
Atrioventricular Block
Atrioventricular Septal Defect
Aural Atresia, Congenital
Autoimmune Disease
Autoimmune Hepatitis
Autoimmune Myocarditis
Autoinflammation, Lipodystrophy, and Dermatosis Syndrome
Autosomal Dominant Polycystic Kidney Disease
Autosomal Recessive Limb-Girdle Muscular Dystrophy
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2e
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2f
Axonal Neuropathy
Bacterial Meningitis
Bardet-Biedl Syndrome
Barth Syndrome
Benign Chronic Pemphigus
Beriberi
Beryllium Disease
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
Bone Fracture
Bone Inflammation Disease
Borjeson-Forssman-Lehmann Syndrome
Brachydactyly
Breast Cancer
Bronchiolitis Obliterans
Brucellosis
Cardiac Arrest
Cardiac Conduction Defect
Cardiac Conduction Disease with or Without Dilated Cardiomyopathy
Cardiac Sarcoidosis
Cardiac Valvular Defect, Developmental
Cardiogenic Shock
Cardiomyopathy Cataract Hip Spine Disease
Cardiomyopathy, Dilated, 1a
Cardiomyopathy, Dilated, 1b
Cardiomyopathy, Dilated, 1d
Cardiomyopathy, Dilated, 1dd
Cardiomyopathy, Dilated, 1e
Cardiomyopathy, Dilated, 1o
Cardiomyopathy, Dilated, 1x
Cardiomyopathy, Dilated, 3b
Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism
Cardiomyopathy, Dilated, with Woolly Hair and Keratoderma
Cardiomyopathy, Familial Hypertrophic, 1
Cardiomyopathy, Familial Hypertrophic, 4
Cardiomyopathy, Familial Restrictive, 1
Cardioneuromyopathy with Hyaline Masses and Nemaline Rods
Carnitine Deficiency, Systemic Primary
Carotid Artery Disease
Carotid Stenosis
Cataract
Catastrophic Antiphospholipid Syndrome
Catecholaminergic Polymorphic Ventricular Tachycardia
Celiac Disease 1
Central Nervous System Vasculitis
Central Sleep Apnea
Centronuclear Myopathy
Cerebellofaciodental Syndrome
Cerebritis
Cervicitis
Chagas Disease
Chlamydia
Cholangitis
Cholestasis
Chorea, Childhood-Onset, with Psychomotor Retardation
Choreatic Disease
Chorioamnionitis
Chronic Fatigue Syndrome
Churg-Strauss Syndrome
Chylothorax, Congenital
Clonorchiasis
Cocaine Abuse
Colitis
Compartment Syndrome
Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy
Complex Regional Pain Syndrome
Conduct Disorder
Congenital Cytomegalovirus
Congenital Disorder of Glycosylation, Type Ic
Congenital Disorder of Glycosylation, Type Im
Congenital Fiber-Type Disproportion
Congenital Generalized Lipodystrophy
Congestive Heart Failure
Conjunctivitis
Conjunctivochalasis
Connective Tissue Disease
Contact Dermatitis
Corneal Dystrophy, Fleck
Coronary Artery Anomaly
Coronary Stenosis
Cor Triatriatum
Creatine Phosphokinase, Elevated Serum
Crouzon Syndrome with Acanthosis Nigricans
Cystic Echinococcosis
Cytomegalovirus Infection
Danon Disease
Darier-White Disease
Dengue Hemorrhagic Fever
Denys-Drash Syndrome
Diabetic Foot Ulcers
Diarrhea
Diastolic Heart Failure
Diffuse Cutaneous Mastocytosis
Digeorge Syndrome
Dirofilariasis
Distal Arthrogryposis
Double-Orifice Mitral Valve
Dystrophinopathies
Eales Disease
Eating Disorder
Ebstein Anomaly
Echinococcosis
Ectodermal Dysplasia
Ectodermal Dysplasia/skin Fragility Syndrome
Ehlers-Danlos Syndrome
Emerinopathy
Emery-Dreifuss Muscular Dystrophy
Encephalopathy
Endocardial Fibroelastosis
Endocarditis
Endometritis
Endomyocardial Fibroelastosis
Endomyocardial Fibrosis
Endotheliitis
End Stage Renal Failure
Epidermolysis Bullosa
Epidermolysis Bullosa Dystrophica
Epidermolysis Bullosa, Lethal Acantholytic
Epidermolysis Bullosa Simplex
Epidermolysis Bullosa Simplex with Muscular Dystrophy
Epilepsy
Epiphyseal Dysplasia, Multiple, 1
Epithelial Recurrent Erosion Dystrophy
Epithelioid Neurofibroma
Essential Thrombocythemia
Extracardiac Rhabdomyoma
Extrinsic Allergic Alveolitis
Extrinsic Cardiomyopathy
Fainting
Familial Hypertension
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
Familial Long Qt Syndrome
Familial Partial Lipodystrophy
Familial Sick Sinus Syndrome
Fascioliasis
Fetal Akinesia Deformation Sequence
Fibromuscular Dysplasia
Fukuyama Type Muscular Dystrophy
Ganglioneuroblastoma
Gapo Syndrome
Gastroenteritis
Giant Cell Myocarditis
Gingival Disease
Gingival Fibromatosis
Gingival Overgrowth
Gingivitis
Gitelman Syndrome
Glucagonoma
Glucose Metabolism Disease
Glucose Transporter Type 1 Deficiency Syndrome
Gout
Graft-Versus-Host Disease
Griscelli Syndrome
Grover's Disease
Growth Hormone Deficiency
Heart Conduction Disease
Heart Disease
Heart Tumor
Heart Valve Disease
Hemihyperplasia, Isolated
Hemolytic-Uremic Syndrome
Hemophagocytic Lymphohistiocytosis, Familial, 2
Hemorrhagic Fever
Hemorrhagic Fever with Renal Syndrome
Hemosiderosis
Hepatic Adenomas, Familial
Hepatic Encephalopathy
Hepatitis
Hepatitis C
Hepatitis C Virus
Hepatopulmonary Syndrome
Hepatorenal Syndrome
Heterotaxy
Hidradenitis
Hidradenitis Suppurativa
Hinman Syndrome
Holt-Oram Syndrome
Hyaline Fibromatosis Syndrome
Hydrolethalus Syndrome 1
Hydrops, Lactic Acidosis, and Sideroblastic Anemia
Hypercholesterolemia, Autosomal Dominant, 3
Hypereosinophilic Syndrome
Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy
Hypertensive Heart Disease
Hyperthyroidism
Hypertrophic Cardiomyopathy
Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1
Hypoaldosteronism
Hypogonadism
Hypoparathyroidism
Hypopituitarism
Hypoplastic Left Heart Syndrome
Hyporeninemic Hypoaldosteronism
Hypoxia
Ichthyosis, Congenital, Autosomal Recessive 11
Ichthyosis Prematurity Syndrome
Idiopathic Hypercalciuria
Idiopathic Neutropenia
Iga Glomerulonephritis
Immunodeficiency 43
Immunoglobulin E Concentration, Serum
Inclusion Body Myositis
Infectious Myocarditis
Inguinal Hernia
Intermittent Claudication
Interstitial Nephritis
Intrahepatic Cholestasis
Intrinsic Cardiomyopathy
Ischemia
Ischemic Heart Disease
Ischemic Optic Neuropathy
Isolated Hyperckemia
Joint Disorders
Juvenile Myasthenia Gravis
Juvenile Rheumatoid Arthritis
Kashin-Beck Disease
Kawasaki Disease
Kearns-Sayre Syndrome
Keratoconjunctivitis Sicca
Keratoderma with Woolly Hair
Keratosis
Keshan Disease
Laryngitis
Left Ventricular Noncompaction
Leptospirosis
Levocardia
Limb-Girdle Muscular Dystrophy
Limbic Encephalitis with Lgi1 Antibodies
Limb Ischemia
Lipid Storage Disease
Lipodystrophy
Liver Cirrhosis
Lmna-Related Dilated Cardiomyopathy
Localized Scleroderma
Loeys-Dietz Syndrome
Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency
Long Qt Syndrome
Long Qt Syndrome 6
Lung Squamous Cell Carcinoma
Lupus Erythematosus
Lyme Disease
Lymph Node Disease
Macular Dystrophy, Retinal, 1, North Carolina Type
Major Affective Disorder 2
Malignant Hypertension
Malignant Hyperthermia
Marfan Syndrome
Mcleod Syndrome
Mediastinitis
Meningitis
Meningococcal Infection
Microcolon
Microscopic Colitis
Microvascular Complications of Diabetes 3
Microvascular Complications of Diabetes 5
Migraine with or Without Aura 1
Miliary Tuberculosis
Mitochondrial Disorders
Mitral Valve Disease
Mixed Connective Tissue Disease
Mohr-Tranebjaerg Syndrome
Mucolipidosis Ii Alpha/beta
Mucolipidosis Iv
Mucopolysaccharidosis-Plus Syndrome
Multiple Endocrine Neoplasia
Mungan Syndrome
Muscle Eye Brain Disease
Muscle Hypertrophy
Muscle Tissue Disease
Muscular Dystrophy
Muscular Dystrophy, Becker Type
Muscular Dystrophy, Congenital, 1b
Muscular Dystrophy, Congenital, Lmna-Related
Muscular Dystrophy, Congenital Merosin-Deficient, 1a
Muscular Dystrophy, Duchenne and Becker Type
Muscular Dystrophy, Duchenne Type
Muscular Dystrophy-Dystroglycanopathy , Type a, 4
Muscular Dystrophy-Dystroglycanopathy , Type B, 5
Muscular Dystrophy-Dystroglycanopathy , Type B, 6
Muscular Dystrophy-Dystroglycanopathy , Type C, 5
Muscular Dystrophy, Limb-Girdle, Type 2a
Muscular Dystrophy, Limb-Girdle, Type 2b
Muscular Dystrophy, Limb-Girdle, Type 2c
Muscular Dystrophy, Limb-Girdle, Type 2d
Muscular Dystrophy, Limb-Girdle, Type 2f
Muscular Dystrophy, Limb-Girdle, Type 2h
Muscular Dystrophy, Limb-Girdle, Type 2j
Myasthenia Gravis
Myocardial Infarction
Myocardial Stunning
Myocarditis
Myofibrillar Myopathy
Myopathy
Myopathy, Centronuclear, 2
Myopathy, Myofibrillar, 1
Myopathy, Myofibrillar, 2
Myopathy, Spheroid Body
Myopathy, X-Linked, with Excessive Autophagy
Myosin Storage Myopathy
Myositis
Myotonia
Myotonic Dystrophy
Naxos Disease
Nemaline Myopathy
Neonatal Lupus Erythematosus
Nephrogenic Systemic Fibrosis
Nephrosclerosis
Neuroblastoma
Neuropathy
Neutropenia
Nonarteritic Anterior Ischemic Optic Neuropathy
Obsessive-Compulsive Disorder
Obstructive Jaundice
Oculodentodigital Dysplasia
Oliver Syndrome
Opportunistic Mycosis
Optic Atrophy 3, Autosomal Dominant
Orthostatic Intolerance
Palmoplantar Keratoderma and Woolly Hair
Palmoplantar Keratoderma, Epidermolytic
Panuveitis
Papillomatosis, Confluent and Reticulated
Paraneoplastic Pemphigus
Patent Foramen Ovale
Pemphigus Vulgaris
Pericardial Effusion
Pericarditis
Perinephritis
Periodontal Disease
Periodontitis
Peripartum Cardiomyopathy
Peripheral Artery Disease
Peritonitis
Phaeochromocytoma
Pheochromocytoma
Pineal Region Choriocarcinoma
Plasmodium Vivax Malaria
Pneumoconiosis
Pneumonia
Portal Hypertension
Posterior Urethral Valves
Prader-Willi Syndrome
Primary Amebic Meningoencephalitis
Primary Systemic Mycosis
Propionic Acidemia
Prostatitis
Protein-Energy Malnutrition
Psoriasis
Psoriasis 13
Pulmonary Aspergilloma
Pulmonary Disease, Chronic Obstructive
Pulmonary Edema
Pulmonary Embolism
Pulmonary Hemosiderosis
Pulmonary Hypertension
Pulmonary Sequestration
Pulmonary Tuberculosis
Pulpitis
Purpura
Pustular Psoriasis
Pyelonephritis
Q Fever
Reactive Arthritis
Recessive Dystrophic Epidermolysis Bullosa
Reducing Body Myopathy
Relapsing-Remitting Multiple Sclerosis
Renal Artery Disease
Renal Fibrosis
Renal Hypertension
Renal Tuberculosis
Renal Tubular Dysgenesis
Renovascular Hypertension
Respiratory System Disease
Resting Heart Rate, Variation in
Restrictive Cardiomyopathy
Retinitis
Rheumatic Disease
Rheumatic Heart Disease
Rheumatoid Arthritis
Rheumatoid Lung Disease
Rheumatoid Nodulosis
Rheumatoid Vasculitis
Rickets
Rubella
Sarcoidosis 2
Schistosomiasis
Schnyder Corneal Dystrophy
Scrub Typhus
Sensorineural Hearing Loss
Severe Combined Immunodeficiency
Sheehan Syndrome
Short Qt Syndrome
Shwachman-Diamond Syndrome
Sick Sinus Syndrome
Silicosis
Silver-Russell Syndrome
Sinoatrial Node Disease
Sleep Apnea
Smallpox
Sorsby Fundus Dystrophy
Spastic Entropion
Spondylitis
Spondyloarthropathy
Spondyloarthropathy 1
Squamous Cell Carcinoma
Squamous Cell Carcinoma of the Hypopharynx
Subacute Cerebellar Degeneration
Superior Limbic Keratoconjunctivitis
Syncope
Syndrome of Inappropriate Antidiuretic Hormone
Synovitis
Systolic Heart Failure
Takayasu Arteritis
Tendinosis
Tetralogy of Fallot
Thrombosis
Thyroiditis
Toxic Shock Syndrome
Toxoplasmoză
Transverse Myelitis
Treacher Collins Syndrome 1
Tropical Endomyocardial Fibrosis
Trypanosomiasis
Tuberous Sclerosis
Turner Syndrome
Type Ii Mixed Cryoglobulinemia
Typhoid Fever
Ulcerative Colitis
Uveitis
Vascular Disease
Vasculitis
Ventricular Fibrillation, Paroxysmal Familial, 1
Ventricular Septal Defect
Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy
Viral Encephalitis
Visceral Heterotaxy
Vogt-Koyanagi-Harada Disease
Walker-Warburg Syndrome
Wolff-Parkinson-White Syndrome
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