Informaţii despre

Nume Coronary Artery Anomaly
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice
Clasificari ICD10 Atherosclerotic heart disease; Chronic ischaemic heart disease, unspecified; Chronic passive congestion of liver
Clasificare anatomică Malacards Boli cardiovasculare
Boli din aceeaşi familie Coronary Artery Disease, Autosomal Dominant 2; Coronary Artery Disease, Autosomal Dominant, 1

Vezi şi

Boli A-Z Aarskog-Scott Syndrome Abdominal Obesity-Metabolic Syndrome 1 Abetalipoproteinemia Ablepharon-Macrostomia Syndrome Acquired Generalized Lipodystrophy Acquired Metabolic Disease Acrocallosal Syndrome Acromegaly Acromelic Frontonasal Dysostosis Acute Anterolateral Myocardial Infarction Acute Cor Pulmonale Acute Kidney Failure Acute Mountain Sickness Acute Myocardial Infarction Acute Pulmonary Heart Disease Adenoma Adrenocortical Carcinoma, Hereditary Aging Aland Island Eye Disease Alcoholic Cardiomyopathy Alopecia Alopecia, Androgenetic, 1 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 19 Alzheimer Disease 2 Alzheimer Disease 3 Amaurosis Fugax Amyloidosis Aa Amyloidosis, Familial Visceral Anauxetic Dysplasia 1 Androgen Insensitivity, Partial Aneurysm Angel-Shaped Phalangoepiphyseal Dysplasia Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Anterolateral Myocardial Infarction Antiphospholipid Syndrome Anuria Aortic Aneurysm Aortic Atherosclerosis Aortic Coarctation Aortic Disease Aortic Valve Insufficiency Aortitis Apert Syndrome Apnea, Obstructive Sleep Apolipoprotein C-Ii Deficiency Apolipoprotein C-Iii Deficiency Arcus Corneae Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Arteries, Anomalies of Arteriosclerosis Arteriosclerosis Obliterans Arteritic Anterior Ischemic Optic Neuropathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Aspirin Resistance Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Telangiectasia Atherosclerosis Susceptibility Atrial Fibrillation Atrioventricular Block Atrophic Gastritis Autonomic Dysfunction Autonomic Neuropathy Axenfeld-Rieger Syndrome B-Cell Lymphomas 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 Bronchiolitis Brugada Syndrome Buerger Disease Cardiac Arrest Cardiac Rupture Cardiac Sarcoidosis Cardiogenic Shock Carotid Artery Disease Carotid Artery Thrombosis Carotid Intimal Medial Thickness 2 Carotid Stenosis Central Sleep Apnea Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 Cerebral Artery Occlusion Cerebral Atherosclerosis Cerebral Hemorrhage Cerebral Palsy, Ataxic, Autosomal Recessive Cerebritis Cerebrotendinous Xanthomatosis Cerebrovascular Disease Chagas Disease Chlamydia Chronic Apical Periodontitis Chronic Fatigue Syndrome Chronic Mountain Sickness Chronic Thromboembolic Pulmonary Hypertension Chronic Venous Insufficiency Clopidogrel Resistance Cocaine Abuse Cold Agglutinin Disease Colorectal Adenoma Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congestive Heart Failure Constrictive Pericarditis Coronary Arterial Fistulas Coronary Artery Aneurysm Coronary Artery Vasospasm Coronary Heart Disease 1 Coronary Stenosis Coronary Thrombosis Creatine Phosphokinase, Elevated Serum Critical Limb Ischemia Crouzon Syndrome with Acanthosis Nigricans Cutis Laxa, Autosomal Recessive, Type Iiia Cytomegalovirus Infection Darier-White Disease Defective Apolipoprotein B-100 Denys-Drash Syndrome Dextrocardia Dextrocardia with Situs Inversus Diabetes Mellitus Diabetes Mellitus, Noninsulin-Dependent Diabetic Angiopathy Diastolic Heart Failure Diastrophic Dysplasia Diffuse Large B-Cell Lymphoma Diffuse Lymphatic Malformation Dilated Cardiomyopathy Dirofilariasis Disseminated Intravascular Coagulation Double Discordia Duane Retraction Syndrome 1 Dubowitz Syndrome Dysbaric Osteonecrosis Earlobe Crease Endocarditis Endotheliitis End Stage Renal Failure Epiglottitis Extrinsic Cardiomyopathy Factor V Deficiency Familial Hyperlipidemia Familial Lcat Deficiency Familial Lipoprotein Lipase Deficiency Fatty Liver Disease Fetal Akinesia Deformation Sequence Fetal Macrosomia Fibrinolytic Defect Fibromuscular Dysplasia First-Degree Atrioventricular Block Fish-Eye Disease Galactose Epimerase Deficiency Gallbladder Disease Gastritis Giant Cell Myocarditis Gingivitis Glucose Intolerance Glucose Metabolism Disease Glycogen Storage Disease Glycogen Storage Disease Iii Goiter Gout Headache Headache Associated with Sexual Activity Heart Disease Helicobacter Pylori Infection Hellp Syndrome Hemophilia Hemophilia B Hemorrhage, Intracerebral Hemosiderosis Henoch-Schoenlein Purpura Heparin Cofactor Ii Deficiency Hepatic Adenomas, Familial Hepatic Lipase Deficiency Hepatic Vascular Disease Hepatitis Hepatorenal Syndrome Hidradenitis Hidradenitis Suppurativa Hinman Syndrome Homocysteinemia Homozygous Familial Hypercholesterolemia Hydrolethalus Syndrome 1 Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperalphalipoproteinemia 1 Hyperandrogenism Hypercholesterolemia, Autosomal Dominant, 3 Hypercholesterolemia, Autosomal Dominant, Type B Hypercholesterolemia, Familial Hyperglycemia Hyperinsulinism Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hyperlipoproteinemia, Type V Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Heart Disease Hypertensive Retinopathy Hyperthyroidism Hypertriglyceridemia, Familial Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia Hypoaldosteronism Hypoalphalipoproteinemia, Primary Hypobetalipoproteinemia, Familial, 1 Hypocalcemia, Autosomal Dominant 1 Hypolipoproteinemia Hypoplastic Left Heart Syndrome Hypoxia Idiopathic Edema Immunoglobulin E Concentration, Serum Impotence Infective Endocarditis Inferior Myocardial Infarction Inferior Vena Cava Interruption Inherited Metabolic Disorder Insulin-Like Growth Factor I Intermittent Claudication Intermittent Explosive Disorder Intracranial Aneurysm Intracranial Vasospasm Ischemia Ischemic Heart Disease Ischemic Optic Neuropathy Kawasaki Disease Lactose Intolerance Lateral Myocardial Infarction Lecithin:cholesterol Acyltransferase Deficiency Left Ventricular Noncompaction Lemierre's Syndrome Leukemia Leukodystrophy, Hypomyelinating, 3 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lichen Sclerosus Limb Ischemia Lipase Deficiency, Combined Lipid Metabolism Disorder Lipoprotein Glomerulopathy Liver Disease Logopenic Progressive Aphasia Long Qt Syndrome Lung Cancer Lupus Erythematosus Lutheran Suppressor, X-Linked Lymphoma Malignant Hypertension Malignant Otitis Externa Malignant Renovascular Hypertension Malignant Secondary Hypertension Marfan Syndrome Mastoiditis Mediastinitis Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration Microvascular Complications of Diabetes 3 Microvascular Complications of Diabetes 5 Middle Cerebral Artery Infarction Mitral Valve Disease Mitral Valve Insufficiency Mitral Valve Stenosis Moderate and Severe Traumatic Brain Injury Mohr-Tranebjaerg Syndrome Morbid Obesity Mucolipidosis Ii Alpha/beta Mucopolysaccharidosis-Plus Syndrome Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Symmetrical Lipomatosis Mungan Syndrome Myocardial Infarction Myocardial Stunning Myocarditis Myxedema Neonatal Stroke Nephrosclerosis Nephrotic Syndrome Neurodegeneration with Brain Iron Accumulation 2a Neuropathy Neutrophil Actin Dysfunction Niemann-Pick Disease Niemann-Pick Disease, Type B Nonalcoholic Steatohepatitis Nonarteritic Anterior Ischemic Optic Neuropathy Nutmeg Liver Obesity-Hypoventilation Syndrome Opioid Abuse Opitz Gbbb Syndrome, Type I Orthostatic Intolerance Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteoporotic Fracture Overnutrition Pancreatitis Panic Disorder Papillon-Lefevre Syndrome Parkinsonism with Spasticity, X-Linked Pericardial Effusion Pericarditis Periodontal Disease Periodontitis Peripheral Artery Disease Peripheral Vascular Disease Peritonitis Phocomelia Pick Disease of Brain Plasminogen Activator Inhibitor-1 Deficiency Platelet Aggregation, Spontaneous Platelet Groups--Ko System Platelet Membrane Fluidity Pneumonia Polycystic Ovary Syndrome Portal Vein Thrombosis Posterior Myocardial Infarction Posterior Urethral Valves Postgastrectomy Syndrome Potocki-Lupski Syndrome Prader-Willi Syndrome Prediabetes Syndrome Premature Menopause Primary Biliary Cirrhosis Primary Lateral Sclerosis, Adult, 1 Prinzmetal's Variant Angina Progressive Familial Heart Block, Type Ib Prostatitis Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak Psoriasis Psoriasis 13 Psoriatic Arthritis Pulmonary Edema Pulmonary Embolism Pulmonary Embolism and Infarction Pulmonary Hypertension Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis Pulmonic Stenosis Pure Autonomic Failure Purpura Renal Artery Disease Renal Glucosuria Renal Hypertension Renal Tubular Acidosis Renal Tubular Dysgenesis Renovascular Hypertension Resting Heart Rate, Variation in Restless Legs Syndrome Retinal Artery Occlusion Retinal Vein Occlusion Retinitis Rheumatic Disease Rheumatic Heart Disease Rheumatoid Arthritis Riboflavin Deficiency Right Bundle Branch Block Salt and Pepper Developmental Regression Syndrome Sarcoidosis 2 Sarcoma Schizoaffective Disorder Schizophrenia Schnyder Corneal Dystrophy Scoliosis, Isolated 1 Sensorineural Hearing Loss Severe Hemophilia B Sick Sinus Syndrome Sinusitis Situs Inversus Sleep Apnea Sleep Disorder Smith-Lemli-Opitz Syndrome Spindle Cell Sarcoma Spondylitis Spondyloarthropathy 1 Spondyloocular Syndrome Sternal Cleft Stroke, Ischemic Substernal Goiter Sveinsson Chorioretinal Atrophy Syncope Syndrome of Inappropriate Antidiuretic Hormone Syringocystadenoma Papilliferum Systemic Lupus Erythematosus Systemic Mastocytosis Systemic Scleroderma Systolic Heart Failure Tangier Disease Tetralogy of Fallot Thrombocytosis Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thymoma Thyroiditis Tick Paralysis Toxic Myocarditis Toxic Shock Syndrome Transposition of the Great Arteries Turner Syndrome Undifferentiated Pleomorphic Sarcoma Uremia Van Der Woude Syndrome 1 Vascular Dementia Vascular Disease Vasculogenic Impotence Venous Insufficiency Ventricular Septal Defect Vibrio Vulnificus Infection Viral Hepatitis Vitamin B12 Deficiency Vitamin E, Familial Isolated Deficiency of Watson Syndrome Werner Syndrome Wolfram Syndrome Xanthoma Disseminatum Xanthomatosis