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Prevalence Statistics for Types of Circulatory system conditions

Prevalence Statistics for Types of Circulatory system conditions

The information below shows a list of types of Circulatory system conditions, with information as to the prevalence of each of these types. Estimates of the people affected are calculated based on the available statistic.

Disease Prevalence Estimate US people estimate Statistic Used for Calculation
Cardiotoxicity -- Halogenated Hydrocarbons N/A N/A No information
Cardiotoxicity -- Organophosphates N/A N/A No information
Cardiotoxicity -- Arsine N/A N/A No information
Cardiotoxicity -- Fluorocarbons N/A N/A No information
Cardiotoxicity -- Propylene Glycol N/A N/A No information
Cardiotoxicity -- Certain Tricyclic Antidepressants N/A N/A No information
Cardiotoxicity -- Ethanol N/A N/A No information
Cardiotoxicity -- Allylamine N/A N/A No information
Cardiotoxicity -- Arsenic N/A N/A No information
Cardiotoxicity -- Ergot alkaloids N/A N/A No information
Cardiotoxicity -- Aromatic hydrocarbons N/A N/A No information
Cardiotoxicity -- Carbon Disulfide N/A N/A No information
Cardiotoxicity -- Carbon Monoxide N/A N/A No information
Cardiotoxicity -- Nitrogen Dioxide N/A N/A No information
Cardiotoxicity -- Ozone N/A N/A No information
Cardiotoxicity -- Hydrogen Chloride N/A N/A No information
Cardiotoxicity -- Ammonia N/A N/A No information
Cardiotoxicity -- Vinyl Chloride N/A N/A No information
Cardiotoxicity -- Thorium Dioxide N/A N/A No information
Chemical-induced cardiovascular disease N/A N/A No information
Carbon disulfide-induced cardiovascular disease N/A N/A No information
Aneurysm, intracranial berry, 10 N/A N/A No information
Aneurysm, intracranial berry, 9 N/A N/A No information
Aneurysmal subarachnoid haemorrhage N/A N/A No information
Aneurysm, intracranial berry N/A N/A No information
Aneurysm, intracranial berry, 1 N/A N/A No information
Aneurysm, intracranial berry, 2 N/A N/A No information
Aneurysm, intracranial berry, 3 N/A N/A No information
Aneurysm, intracranial berry, 4 N/A N/A No information
Aneurysm, intracranial berry, 5 N/A N/A No information
Aneurysm, intracranial berry, 6 N/A N/A No information
Cerebrovascular Conditions approx 1 in 33 or 3.00% or 8.2 million people in USA 8,160,000 30 per 1000 - NHIS95
Stroke approx 1 in 59 or 1.69% or 4.6 million people in USA 4,599,999 estimated 4.6 million (NHLBI)
Artery conditions N/A N/A No information
Aneurysm N/A N/A No information
Abdominal aortic aneurysm N/A N/A No information
Aortic aneurysm N/A N/A No information
Aorta conditions N/A N/A No information
Aortic coarctation N/A N/A No information
Aortic valve disease N/A N/A No information
Arteritis N/A N/A No information
Atherosclerosis approx 1 in 58 or 1.70% or 4.6 million people in USA 4,624,000 17 per 1000 - NHIS95
Embolism N/A N/A No information
Primary pulmonary hypertension N/A N/A No information
Pulmonary embolism N/A N/A No information
Pulmonary hypertension N/A N/A No information
Thromboembolism N/A N/A No information
Angioma N/A N/A No information
Cerebrovascular accident N/A N/A No information
Subconjunctival hemorrhage N/A N/A No information
Extradural hematoma N/A N/A No information
Pulmonary valve stenosis N/A N/A No information
Aortic valve stenosis N/A N/A No information
Aortic stenosis N/A N/A No information
Cardiomyopathy -- hypotonia -- lactic acidosis N/A N/A No information
Cardiomyopathy -- renal anomalies N/A N/A No information
Hypertension headache N/A N/A No information
Vascular headaches N/A N/A No information
Angiosarcoma of the liver N/A N/A No information
Familial hypertrophic cardiomyopathy 1 N/A N/A No information
Familial hypertrophic cardiomyopathy 2 N/A N/A No information
Familial hypertrophic cardiomyopathy 3 N/A N/A No information
Familial hypertrophic cardiomyopathy 4 N/A N/A No information
Familial hypertrophic cardiomyopathy 6 N/A N/A No information
Familial hypertrophic cardiomyopathy 7 N/A N/A No information
Familial hypertrophic cardiomyopathy 8 N/A N/A No information
Familial hypertrophic cardiomyopathy 9 N/A N/A No information
Familial hypertrophic cardiomyopathy 10 N/A N/A No information
Cardiomyopathy dilated 1B N/A N/A No information
Cardiomyopathy dilated 1C N/A N/A No information
Cardiomyopathy dilated 1D N/A N/A No information
Cardiomyopathy dilated 1E N/A N/A No information
Cardiomyopathy dilated 1G N/A N/A No information
Cardiomyopathy dilated 1H N/A N/A No information
Cardiomyopathy dilated 1I N/A N/A No information
Cardiomyopathy dilated 1J N/A N/A No information
Cardiomyopathy dilated 1K N/A N/A No information
Cardiomyopathy dilated 1L N/A N/A No information
Cardiomyopathy dilated 1M N/A N/A No information
Cardiomyopathy dilated 1N N/A N/A No information
Cardiomyopathy dilated 1P N/A N/A No information
Cardiomyopathy dilated 1Q N/A N/A No information
Cardiomyopathy dilated 1R N/A N/A No information
Cardiomyopathy dilated 1S N/A N/A No information
Cardiomyopathy dilated 1T N/A N/A No information
Cardiomyopathy dilated 1U N/A N/A No information
Cardiomyopathy dilated 1W N/A N/A No information
Cardiomyopathy dilated with conduction defect N/A N/A No information
Cardiomyopathy, Alcoholic N/A N/A No information
Cardiomyopathy diabetes deafness N/A N/A No information
Cardiomyopathy dilated 10 N/A N/A No information
Short QT syndrome 1 N/A N/A No information
Short QT syndrome 2 N/A N/A No information
Short QT syndrome 3 N/A N/A No information
Short QT syndrome, familial N/A N/A No information
Blood vessel conditions N/A N/A No information
Heart conditions N/A N/A No information
Heart disease approx 1 in 12 or 8.09% or 22 million people in USA 21,999,998 22 million adults in the US 2000 (Centers for Disease Control and Prevention)
Cardiovascular Disease approx 1 in 4 or 22.72% or 61.8 million people in USA 61,800,001 61,800,000 cases in the USA (American Heart Association, 2004)
Hypertension approx 1 in 5 or 18.38% or 50 million people in USA 49,999,999 50 million Americans (NHLBI); 217 per 1000 (NHIS95)
Hypertension in children N/A N/A No information
Hypertension in children from 11 through adolescence N/A N/A No information
Hypertension in children one to ten years N/A N/A No information
Hypertension in children under one year N/A N/A No information
Hypertension-like disorders N/A N/A No information
Primary Hypertension N/A N/A No information
Secondary Hypertension N/A N/A No information
Gestational hypertension N/A N/A No information
Eclampsia N/A N/A No information
Malignant hypertension N/A N/A No information
Hypotension N/A N/A No information
Orthostatic hypotension N/A N/A No information
Isolated systolic hypertension N/A N/A No information
Accelerated hypertension N/A N/A No information
Antepartum Eclampsia N/A N/A No information
Postpartum Eclampsia N/A N/A No information
White coat hypertension N/A N/A No information
Hypertension of pregnancy N/A N/A No information
Intrapartum Eclampsia N/A N/A No information
Microvascular Complications of Diabetes, Susceptibility to, 2 N/A N/A No information
Microvascular Complications of Diabetes, Susceptibility to, 3 N/A N/A No information
Microvascular Complications of Diabetes, Susceptibility to, 4 N/A N/A No information
Microvascular Complications of Diabetes, Susceptibility to, 5 N/A N/A No information
Microvascular Complications of Diabetes, Susceptibility to, 6 N/A N/A No information
Microvascular Complications of Diabetes, Susceptibility to, 7 N/A N/A No information
Microvascular Complications of Diabetes, Susceptibility to, 1 N/A N/A No information
Microvascular Complications of Diabetes, Susceptibility to N/A N/A No information
Hypertension, Essential, Susceptibility to, 8 N/A N/A No information
Hypertension, Essential, Susceptibility to, 7 N/A N/A No information
Hypertension, Essential, Susceptibility to, 6 N/A N/A No information
Hypertension, Essential, Susceptibility to, 5 N/A N/A No information
Hypertension, Essential, Susceptibility to, 4 N/A N/A No information
Hypertension, Essential, Susceptibility to, 3 N/A N/A No information
Hypertension, Essential, Susceptibility to, 2 N/A N/A No information
Hypertension, Essential N/A N/A No information
Hypertension, Essential, Susceptibility to N/A N/A No information
Hypertension, Essential, Susceptibility to, 1 N/A N/A No information
Liver vein outflow obstruction N/A N/A No information
Right atrium familial dilatation N/A N/A No information
Mental retardation -- short stature -- heart and skeletal anomalies N/A N/A No information
Portal hypertension N/A N/A No information
Vein disorders N/A N/A No information
Varicose veins approx 1 in 22 or 4.50% or 12.2 million people in USA 12,240,000 45 per 1000 (NHIS95)
Legg-Calve-Perthes disease N/A N/A No information
Atrial Fibrillation approx 1 in 136 or 0.74% or 2 million people in USA 1,999,999 2 million (NHLBI)
Atrial flutter N/A N/A No information
Bradycardia N/A N/A No information
Cardiac arrest N/A N/A No information
Cardiomyopathy approx 1 in 5,439 or 0.02% or 50,000 people in USA 50,000 50,000 Americans (NHLBI)
Congestive Heart Failure approx 1 in 56 or 1.76% or 4.8 million people in USA 4,800,000 4.8 million Americans (NHLBI); 2% age 40-59; 5% age 60-69; 10% over 70's
Dilated cardiomyopathy N/A N/A No information
Endocarditis N/A N/A No information
Heart block N/A N/A No information
Heart valve diseases N/A N/A No information
Hypertrophic cardiomyopathy approx 1 in 500 or 0.20% or 544,000 people in USA 544,000 0.2 percent of the U.S. population
Left heart failure N/A N/A No information
Mitral regurgitation N/A N/A No information
Mitral stenosis N/A N/A No information
Mitral valve disease N/A N/A No information
Myocarditis N/A N/A No information
Palpitations N/A N/A No information
Pericarditis N/A N/A No information
Pulmonary valve disease N/A N/A No information
Restrictive cardiomyopathy N/A N/A rare
Right heart failure N/A N/A No information
Tricuspid valve disease N/A N/A No information
Heart cancer N/A N/A No information
Atrial Fibrillation, Familial 8 N/A N/A No information
Atrial Fibrillation, Familial 7 N/A N/A No information
Atrial Fibrillation, Familial 6 N/A N/A No information
Atrial Fibrillation, Familial 5 N/A N/A No information
Atrial Fibrillation, Familial 4 N/A N/A No information
Atrial Fibrillation, Familial 3 N/A N/A No information
Atrial Fibrillation, Familial 2 N/A N/A No information
Renal Failure, Progressive, with Hypertension N/A N/A No information
Progressive nephropathy with hypertension, autosomal dominant N/A N/A No information
Familial hypertrophic cardiomyopathy 12 N/A N/A No information
Familial hypertrophic cardiomyopathy 11 N/A N/A No information
Familial hypertrophic cardiomyopathy 5 N/A N/A No information
Decreased vascularity N/A N/A No information
Mitral valve prolapse, familial N/A N/A No information
Idiopathic neonatal atrial flutter N/A N/A No information
Varicose eczema N/A N/A No information
Hemorrhagic prostatic cyst N/A N/A No information
Cocaine-induced hypertension N/A N/A No information
Pulmonary venous hypertension N/A N/A No information
Hypertension due to bilateral renal artery stenosis N/A N/A No information
Labile Hypertension N/A N/A No information
Alcohol-induced hypertension N/A N/A No information
Primary pulmonary hypertension -- Dexfenfluramine-associated N/A N/A No information
Amphetamine-induced hypertension N/A N/A No information
Kidney disease-Induced Hypertension N/A N/A No information
Nasal decongestant-induced hypertension N/A N/A No information
Hyperaldosteronism-induced hypertension N/A N/A No information
Pulmonary thromboembolic hypertension N/A N/A No information
Resistant hypertension N/A N/A No information
Familial pulmonary arterial hypertension N/A N/A No information
Cushing's syndrome-induced hypertension N/A N/A No information
Pheochromocytoma-induced hypertension N/A N/A No information
Stress-Induced Hypertension N/A N/A No information
Cyclosporine-induced hypertension N/A N/A No information
Corticosteroid-induced hypertension N/A N/A No information
Renal segmental hypoplasia-induced Hypertension N/A N/A No information
Exercise-induced hypertension N/A N/A No information
Prehypertension N/A N/A No information
Rebound hypertension N/A N/A No information
Renovascular Hypertension N/A N/A No information
Hypertension due to coarctation of the aorta N/A N/A No information
Posthemorrhagic anemia N/A N/A No information
Pulmonary hypoxic hypertension N/A N/A No information
Primary pulmonary hypertension -- Fenfluramine-associated N/A N/A No information
Licorice-induced hypertension N/A N/A No information
Drug-induced hypertension N/A N/A No information
Raynaud's phenomenon approx 1 in 20 or 5.00% or 13.6 million people in USA 13,600,000 5-10% (NIAMS estimate). Scleroderma-related disorders including Raynaud's phenomenon between 250,000 and 992,500.
Hemodialysis N/A N/A No information
Autoimmune Myocarditis N/A N/A No information
Autoimmune Vasculitis N/A N/A No information
Autoimmune Atherosclerosis N/A N/A No information
Behcet's Disease N/A N/A rare in the USA; more common in Middle East, Asia, and Japan.
Supraventricular Tachycardia N/A N/A No information
Renal Artery Stenosis N/A N/A No information
Sinus bradycardia N/A N/A No information
Paroxysmal atrial tachycardia N/A N/A No information
Congenital heart septum defect N/A N/A No information
Vascular neuropathy N/A N/A No information
Mental retardation, keratoconus, febrile seizures, and sinoatrial block N/A N/A No information
Vasculitis N/A N/A No information
Multi-Infarct Dementia N/A N/A No information
Smokers Syndrome N/A N/A No information
Heart valve disorder N/A N/A No information
Ehlers-Danlos syndrome, progeroid form N/A N/A No information
Ehlers-Danlos syndrome with periventricular heterotopia N/A N/A No information
Shock, Cardiogenic N/A N/A No information
Shock, Hemorrhagic N/A N/A No information
Shock, Hypovolaemic N/A N/A No information
Shock, Neurogenic N/A N/A No information
Shock, Septic N/A N/A No information
Shock, Traumatic N/A N/A No information
Shock, Obstructive N/A N/A No information
Shock, anaphylactic N/A N/A No information
Shock, Endocrine N/A N/A No information
Shock, Distributive N/A N/A No information
Venous Insufficiency N/A N/A No information
Venous Thrombosis N/A N/A No information
Intracranial Hemorrhages N/A N/A No information
Bilateral stroke N/A N/A No information
Basilar artery insufficiency N/A N/A No information
Stroke-like dysarthria N/A N/A No information
Intraocular hemorrhage N/A N/A No information
Pheochromocytoma-like persistent hypertension N/A N/A No information
Chronic orthostatic hypotension N/A N/A No information
Systolic ejection murmur N/A N/A No information
Mottled cyanosis N/A N/A No information
Drop attacks as seen in stroke N/A N/A No information
Palpable thrill as in case of valvular heart disease N/A N/A No information
Aberrant subclavian artery abnormality N/A N/A No information
Absence of pulmonary artery N/A N/A No information
Ehlers-Danlos syndrome type X N/A N/A No information
Ehlers-Danlos syndrome, 6B N/A N/A No information
Ehlers-Danlos syndrome approx 1 in 250,000 or 0.00% or 1,087 people in USA 1,087 estimated 1 per 250,000 people suffer from the vascular type of Ehlers-Danlos syndrome, Genetics Home Reference website
Ehlers-Danlos syndrome, progeroid form 2 N/A N/A No information
Ehlers-Danlos syndrome type II N/A N/A No information
Ehlers-Danlos syndrome type IV N/A N/A No information
Ehlers-Danlos syndrome type IX N/A N/A No information
Ehlers-Danlos syndrome, vascular type N/A N/A No information
Ehlers-Danlos syndrome, dermatospraxis type N/A N/A No information
Ehlers-Danlos syndrome, kyphoscoliosis type N/A N/A No information
Ehlers-Danlos syndrome, cardiac valvular form N/A N/A No information
Ehlers-Danlos syndrome type III N/A N/A No information
Ehlers-Danlos syndrome, classic type N/A N/A No information
Ehlers-Danlos syndrome Type I N/A N/A No information
Ehlers-Danlos syndrome, VIIB N/A N/A No information
Ehlers-Danlos Syndrome, Dysfibronectinemic type N/A N/A No information
Ehlers-Danlos syndrome with Platelet Dysfunction from Fibronectin Abnormality N/A N/A No information
Ehlers-Danlos syndrome type VII N/A N/A No information
Ehlers Danlos syndrome type 4, autosomal dominant N/A N/A No information
Ehlers-Danlos syndrome type 3 N/A N/A No information
Ehlers-Danlos syndrome type 4 N/A N/A No information
Arteriovenous fistula N/A N/A No information
Postoperative Hemorrhage N/A N/A No information
Cerebral hemorrhage N/A N/A No information
CREST syndrome N/A N/A No information
Telangiectasia N/A N/A No information
Kawasaki disease N/A N/A No information
Vasovagal attack N/A N/A No information
Subarachnoid haemorrhage N/A N/A No information
Hemorrhage N/A N/A No information
Postpartum hemorrhage N/A N/A No information
Hemoptysis N/A N/A No information
Hematemesis N/A N/A No information
Osler's disease N/A N/A No information
Air embolism N/A N/A No information
Postoperative pulmonary embolism N/A N/A No information
Pulmonary embolus N/A N/A No information
Pulmonary heart disease N/A N/A No information
Secondary pulmonary hypertension approx 1 in 272,000 or 0.00% or 1,000 people in USA 1,000 about 1,000 new cases of pulmonary arterial hypertension are diagnosed each year in the US, Genetics Home Reference website
Hemothorax N/A N/A No information
Circulatory disorder N/A N/A No information
Hemorrhoids approx 1 in 26 or 3.82% or 10.4 million people in USA 10,400,000 10.4 million people in the USA 1983-87 (Digestive diseases in the United States: Epidemiology and Impact NIH Publication No. 94-1447, NIDDK, 1994)
Thrombosis N/A N/A No information
Teleangiectasia N/A N/A No information
Coronary heart disease approx 1 in 20 or 4.85% or 13.2 million people in USA 13,199,999 estimated 13,200,000 in the USA 2001 (American Heart Association, 2004)
Deep vein thrombosis N/A N/A No information
Atheroma N/A N/A No information
Transient tachycardia N/A N/A No information
Severe heart problems N/A N/A No information
Mild hypotension N/A N/A No information
Serious heart arrhythmias N/A N/A No information
Hemangioma N/A N/A No information
Caterpillar-induced bleeding syndrome N/A N/A No information
Caterpillar-induced bleeding syndrome -- Lonomia achelous N/A N/A No information
Caterpillar-induced bleeding syndrome -- Lonomia obliqua N/A N/A No information
Arteriovenous Malformation N/A N/A No information
Congenital heart defects approx 1 in 272 or 0.37% or 1 million people in USA 2,266,666 1 million (NHLBI)
Sino-auricular heart block N/A N/A No information
Long QT syndrome type 9 N/A N/A No information
Pregnancy toxemia /hypertension N/A N/A No information
Short stature -- valvular heart disease N/A N/A No information
Nosebleeds N/A N/A No information
Varicose ulcers N/A N/A No information
Epilepsy -- telangiectasia N/A N/A No information
Short stature valvular heart disease characteristic facies N/A N/A No information
Brachydactyly -- mesomelia -- mental retardation -- heart defects N/A N/A No information
Klippel Trenaunay Weber syndrome N/A N/A No information
Klippel-Trenaunay Syndrome N/A N/A No information
Intracranial aneurysms -- multiple congenital anomaly N/A N/A No information
Angiokeratoma -- mental retardation -- coarse face N/A N/A No information
Microcephaly -- seizures -- mental retardation -- heart disorders N/A N/A No information
Deafness peripheral -- neuropathy -- arterial disease N/A N/A No information
Aortic arch anomaly with peculiar facies and mental retardation N/A N/A No information
Short limbs -- abnormal face -- congenital heart disease N/A N/A No information
Congenital heart disease radio ulnar synostos mental retardation N/A N/A No information
Macrocephaly mesodermal hamartoma spectrum N/A N/A No information
Portal vein thrombosis N/A N/A No information
Midface hypoplasia, corneal clouding, subvalvular aortic stenosis and mental and somatic retardation N/A N/A No information
Arrhythmogenic right ventricular dysplasia, familial, 2 N/A N/A No information
Arrhythmogenic right ventricular dysplasia, familial, 3 N/A N/A No information
Arrhythmogenic right ventricular dysplasia, familial, 1 N/A N/A No information
Arrhythmogenic right ventricular dysplasia, familial, 4 N/A N/A No information
Arrhythmogenic right ventricular dysplasia, familial, 7 N/A N/A No information
Arrhythmogenic right ventricular dysplasia, familial, 8 N/A N/A No information
Aortic Valve Insufficiency N/A N/A No information
Arrhythmogenic right ventricular dysplasia, familial, 9 N/A N/A No information
Arrhythmogenic right ventricular dysplasia, familial, 10 N/A N/A No information
Arrhythmogenic right ventricular dysplasia, familial, 11 N/A N/A No information
Arrhythmogenic right ventricular dysplasia, familial, 12 N/A N/A No information
Cardiomyopathy dilated 1Y N/A N/A No information
Cardiomyopathy dilated 1Z N/A N/A No information
Cardiomyopathy dilated with conduction defect type 1 N/A N/A No information
Cardiomyopathy dilated with conduction defect type 2 N/A N/A No information
Radiation induced angiosarcoma of the breast N/A N/A No information
Cardiomyopathy, familial dilated N/A N/A No information
Familial dilated cardiomyopathy N/A N/A No information
Cerebral Aneurysm N/A N/A No information
Cerebral Arteriosclerosis N/A N/A No information
Heart failure approx 1 in 56 or 1.76% or 4.8 million people in USA 4,800,000 4.8 million (NHLBI); 2 to 3 million Americans (NHLBI)
Heart injury N/A N/A No information
Arrhythmias approx 1 in 18 or 5.30% or 14.4 million people in USA 14,416,000 53 per 1000 (NHIS95: heart rhythm disorders); 21 per 1000 (NHIS95: heart murmurs)
Heart attack approx 1 in 36 or 2.76% or 7.5 million people in USA 7,499,999 7.5 million people with AMI (NHLBI)
Heart Murmur N/A N/A No information
Ischemic heart disease approx 1 in 14 or 6.80% or 18.5 million people in USA 18,496,000 68 per 1000 (NHIS95)
Hypertensive heart disease N/A N/A No information
Aortic valve incompetence N/A N/A No information
Murmur N/A N/A No information
Atrial arrhythmia N/A N/A No information
Sinus arrhythmia N/A N/A No information
Sinus tachycardia N/A N/A No information
Ventricular arrhythmia N/A N/A No information
Ventricular tachycardia N/A N/A No information
Blue veins N/A N/A No information
Ventricular septal defect N/A N/A No information
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy N/A N/A No information
Congenital Lipomatous Overgrowth, Vascular Malformations, Epidermal Nevi, and Skeletal/Spinal abnormalities N/A N/A No information
Congenital Lipomatous Overgrowth, Vascular Malformations and Epidermal Nevi N/A N/A No information
Renovascular stenosis N/A N/A No information
Vascular retinopathies N/A N/A No information
Tetralogy of Fallot N/A N/A No information
Arterial occlusive disease N/A N/A No information
Transposition of the great arteries N/A N/A No information
Renal infarction N/A N/A No information
Venous hum N/A N/A No information
Homans' sign N/A N/A No information
Jugular vein distention N/A N/A No information
Gallop, atrial N/A N/A No information
Gallop, ventricular N/A N/A No information
Atrial Septal Defect N/A N/A No information
Arterial insufficiency N/A N/A No information
Acrocyanosis N/A N/A No information
Polyarteritis N/A N/A No information
Pulsus bisferiens N/A N/A No information
Capillary refill time, increased N/A N/A No information
Sternal malformation vascular dysplasia association N/A N/A No information
Angina approx 1 in 42 or 2.35% or 6.4 million people in USA 6,400,000 6.4 million Americans (NHLBI)
Angina Pectoris N/A N/A No information
Unstable angina N/A N/A No information
Microvascular angina N/A N/A No information
Prinzmetal's variant angina N/A N/A No information
Pulmonary Hypertension, Primary, 1 N/A N/A No information
Pulmonary valves agenesis N/A N/A No information
Adrenal hypertension N/A N/A No information
Familial hypertension N/A N/A No information
Heart block progressive, familial N/A N/A No information
Long QT syndrome type 2 N/A N/A No information
Long QT syndrome type 3 N/A N/A No information
Right ventricle hypoplasia N/A N/A No information
Syncopal paroxysmal tachycardia N/A N/A No information
Doxorubicin-induced cardiomyopathy N/A N/A No information
Cardiomyopathy due to anthracyclines N/A N/A No information
Aneurysm, intracranial berry, 7 N/A N/A No information
Retinal Arterial Occlusion N/A N/A No information
Ventricular tachycardia, catecholaminergic polymorphic, 1 N/A N/A No information
Ventricular tachycardia, catecholaminergic polymorphic, 2 N/A N/A No information
Noonan syndrome 3 N/A N/A No information
Noonan-like/multiple giant cell lesion syndrome N/A N/A No information
Noonan-like syndrome N/A N/A No information
Neurofibromatosis-Noonan syndrome N/A N/A No information
Noonan Syndrome approx 1 in 1,000 or 0.10% or 272,000 people in USA 272,000 estimated 1 per 1,000 - 2,500 people are affected by Noonan syndrome, Genetics Home Reference website
Laryngeal web congenital heart disease short stature N/A N/A No information
Corneal anesthesia deafness mental retardation N/A N/A No information
Corneal anesthesia deafness intellectual deficit N/A N/A No information
Corneal hypesthesia deafness intellectual deficit N/A N/A No information
Atrial Septal Defect 6 N/A N/A No information
Atrial Septal Defect 5 N/A N/A No information
Atrial Septal Defect 4 N/A N/A No information
Atrial Septal Defect 3 N/A N/A No information
Neurogenic hypertension N/A N/A No information
Coronary artery aneurysm N/A N/A No information
Coronary arteries -- congenital malformation N/A N/A No information
Coronary artery disease, autosomal dominant 1 N/A N/A No information
Coronary heart disease, susceptibility to, 1 N/A N/A No information
Coronary artery disease, autosomal dominant 2 N/A N/A No information
Coronary heart disease, susceptibility to, 2 N/A N/A No information
Coronary heart disease, susceptibility to, 3 N/A N/A No information
Coronary heart disease, susceptibility to, 4 N/A N/A No information
Coronary heart disease, susceptibility to, 5 N/A N/A No information
Coronary heart disease, susceptibility to, 7 N/A N/A No information
Coronary heart disease, susceptibility to, 8 N/A N/A No information
Coronary heart disease, susceptibility to, 6 N/A N/A No information
Coronary heart disease, susceptibility to, 9 N/A N/A No information
Aortic aneurysm, familial thoracic 1 N/A N/A No information
Aortic aneurysm, familial thoracic 2 N/A N/A No information
Aortic aneurysm, familial thoracic 3 N/A N/A No information
Aortic aneurysm, familial thoracic 4 N/A N/A No information
Aortic aneurysm, familial thoracic 5 N/A N/A No information
Aortic aneurysm, familial abdominal 1 N/A N/A No information
Aortic aneurysm, familial abdominal 2 N/A N/A No information
Aortic aneurysm, familial abdominal 3 N/A N/A No information
Aortic Aneurysm, Thoracic N/A N/A No information
Atrial fibrillation, familial 1 N/A N/A No information
Portal thrombosis N/A N/A No information
Long QT syndrome type 5 N/A N/A No information
Long QT syndrome type 6 N/A N/A No information
Long QT syndrome type 4 N/A N/A No information
Long QT syndrome, familial N/A N/A No information
Long QT Syndrome 12 N/A N/A No information
Long QT syndrome N/A N/A No information
Long QT syndrome type 10 N/A N/A No information
Long QT syndrome type 11 N/A N/A No information
Ventricular fibrillation N/A N/A No information
Mitral-valve prolapse approx 1 in 50 or 2.00% or 5.4 million people in USA 5,440,000 2% of the adult population (NHLBI estimate)
Tricuspid valve diseases N/A N/A No information
Ventricular Fibrillation, Paroxysmal Familial, 1 N/A N/A No information
Ventricular Fibrillation, Paroxysmal Familial, 2 N/A N/A No information
Ventricular fibrillation, idiopathic N/A N/A No information
Paroxysmal ventricular fibrillation N/A N/A No information
Arrhythmogenic right ventricular dysplasia, familial, 5 N/A N/A No information
Arrhythmogenic right ventricular dysplasia, familial, 6 N/A N/A No information
Arrhythmogenic right ventricular dysplasia N/A N/A No information
Amyloidosis VI N/A N/A No information
Amyloidosis, cerebroarterial, hereditary, Italian type N/A N/A No information
Amyloidosis VII N/A N/A No information
Amyloidosis, oculoleptomeningeal N/A N/A No information
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type N/A N/A No information
Brachydactyly with hypertension N/A N/A No information
Brachydactyly -- arterial hypertension N/A N/A No information
Atrial septal defect 1 N/A N/A No information
Atrial septal defect 2 N/A N/A No information
Atrial septal defect atrioventricular conduction N/A N/A No information
Lymphoedema -- atrial septal defects -- facial changes N/A N/A No information
Hemorrhagic proctocolitis N/A N/A No information
Esophageal varices N/A N/A No information
Dexamethasone sensitive hypertension N/A N/A No information
Congenital mitral stenosis N/A N/A No information
Atrioventricular Septal Defects N/A N/A No information
Atrioventricular septal defect N/A N/A No information
Hypoplastic Left Heart Syndrome N/A N/A No information
Heart defects -- limb shortening N/A N/A No information
Heart-hand syndrome, Spanish type N/A N/A No information
Heart-hand syndrome, Slovenian type N/A N/A No information
Holt-Oram Syndrome approx 1 in 100,000 or 0.00% or 2,720 people in USA 2,720 estimated 1 per 100,000 people suffer from Holt-Oram disease, Genetics Home Reference website
Aorto-ventricular tunnel N/A N/A No information
Hemorrhagic thrombocythemia N/A N/A No information
Essential thrombocytopenia N/A N/A No information
Essential thrombocytosis -- same as essential thrombocythemia N/A N/A No information
Maternally inherited diabetes and deafness with cardiomyopathy N/A N/A No information
Aortic valves stenosis of the child N/A N/A No information
Lipoatrophy with diabetes, hepatic steatosis, cardiomyopathy, and leukomelanodermic papules N/A N/A No information
Atherosclerosis- deafness -- diabetes -- epilepsy -- nephropathy N/A N/A No information
Atherosclerosis, premature -- deafness -- diabetes mellitus -- photomyoclonus -- nephropathy -- degenerative neurologic disease N/A N/A No information
Familial atrial fibrillation approx 1 in 3 or 30.00% or 81.6 million people in USA 81,600,000 estimated 30% of cases of atrial fibrillation are inherited (familial), Genetics Home Reference website
Congenital heart block N/A N/A No information
Wyburn-Mason Syndrome N/A N/A No information
Wyburn Mason's syndrome N/A N/A No information
Coarctation of aorta autosomal dominant N/A N/A No information
Craniosynostosis -- congenital heart disease -- mental retardation N/A N/A No information
Cardiomyopathy with myopathy due to COX deficiency N/A N/A No information
Legg-Calve-Perthes syndrome N/A N/A No information
Cardiomyopathy -- hypogonadism -- metabolic anomalies N/A N/A No information
Pylephlebitis N/A N/A No information
Hyperpigmentation, Cutaneous, With Hypertrichosis, Hepatosplenomegaly, Heart Anomalies, Hearing Loss, And Hypogonadism N/A N/A No information
Wegener's granulomatosis N/A N/A uncommon
Antiphospholipid syndrome N/A N/A No information
Streptococcal Toxic Shock Syndrome N/A N/A No information
Meningococcemia N/A N/A No information
Sacral meningocele -- conotruncal heart defects N/A N/A No information
Vocal cord hemorrhage N/A N/A No information
Woolly hair -- palmoplantar keratoderma -- dilated cardiomyopathy N/A N/A No information
Postoperative haemorrhage N/A N/A No information
Postpartum haemorrhage N/A N/A No information
Calcific aortic disease with immunologic abnormalities, familial N/A N/A No information
Cardiac compression syndrome N/A N/A No information
Cerebral cavernous malformations approx 1 in 200 or 0.50% or 1.4 million people in USA 1,360,000 0.5% of people suffer from cerebral cavernous malformations worldwide, Genetics Home Reference website
Cardiomyopathy with myopathy due to COX deficency N/A N/A No information
Cardiomyopathy, hypogonadism, collagenoma syndrome N/A N/A No information
Vacuolar Cardiomyopathy and Myopathy, X-linked N/A N/A No information
Severe dilated cardiomyopathy with or without myopathy N/A N/A No information
Cardiomyopathy -- hearing loss, type tRNA-LYS gene mutation N/A N/A No information
Cirrhotic cardiomyopathy N/A N/A No information
Peripartum cardiomyopathy N/A N/A No information
Cardiomyopathy dilated 3B N/A N/A No information
Cardiomyopathy dilated 2A N/A N/A No information
Atrial cardiomyopathy with heart block N/A N/A No information
Myopathy, early-onset with fatal cardiomyopathy N/A N/A No information
Chagas Cardiomyopathy N/A N/A No information
Cardiomyopathy, dilated, with Woolly hair and keratoderma N/A N/A No information
Cardiomyopathy, infantile histiocytoid N/A N/A No information
Cardiomyopathy, X-linked, fatal infantile N/A N/A No information
Cataract and cardiomyopathy N/A N/A No information
Cardiomyopathy -- hearing loss, type t RNA lysine gene mutation N/A N/A No information
Idiopathic dilation cardiomyopathy N/A N/A No information
Cardiomyopathy, fatal fetal, due to myocardial calcification N/A N/A No information
Cardiomyopathy -- spherocytosis N/A N/A No information
Genital anomaly -- cardiomyopathy N/A N/A No information
Fibromuscular dysplasia of arteries N/A N/A No information
Microphthalmia diaphragmatic hernia Fallot N/A N/A No information
Hypogonadism -- mitral valve prolapse -- mental retardation N/A N/A No information
Angiosarcoma of the breast N/A N/A No information
Decreased cardiac output N/A N/A No information
Decreased cerebral perfusion N/A N/A No information
Osler-Rendu-Weber syndrome 2 N/A N/A No information
Osler-Rendu-Weber syndrome 3 N/A N/A No information
Aortic arch interruption N/A N/A No information
Congenital heart disease -- radio ulnar synostosis -- mental retardation N/A N/A No information
Amaurosis fugax N/A N/A No information
Common ventricle N/A N/A No information
Familial ventricular tachycardia N/A N/A No information
Hirschsprung disease -- polydactyly -- heart disease N/A N/A No information
Velocardiofacial syndrome N/A N/A No information
DiGeorge's syndrome N/A N/A No information
DiGeorge syndrome N/A N/A No information
Deletion 22q11 N/A N/A No information
Chromosome 22q11 Deletion Spectrum N/A N/A No information
CATCH 22 N/A N/A No information
Shprintzen syndorme N/A N/A No information
$22q11.2 deletion syndrome$ N/A N/A No information
Chromosome 22q11.2 deletion syndrome approx 1 in 4,000 or 0.03% or 68,000 people in USA 68,000 estimated 1 per 4,000 newborns are affected by chromosome 22q11.2 deletion syndrome, Genetics Home Reference website
Chromosome 22q11 deletion N/A N/A No information
Distichiasis with Congenital Anomalies of the heart and Peripheral Vasculature N/A N/A No information
Von Hippel-Lindau Disease N/A N/A rare
Dejerine-Roussy syndrome N/A N/A No information
Angiodysplasia N/A N/A No information
Angiectasis pregnancy N/A N/A No information
Amyloid cardiopathy N/A N/A No information
Atypical coarctation of aorta N/A N/A No information
Mitral valve prolapse, familial, autosomal dominant N/A N/A No information
Glomerulonephritis -- sparse hair -- telangiectases N/A N/A No information
Postural orthostatic tachycardia syndrome N/A N/A No information
Pulmonary arteriovenous malformation N/A N/A No information
Splenic infarcts N/A N/A No information
Hypoplastic right heart -- microcephaly N/A N/A No information
Pulmonary artery agenesis N/A N/A No information
Transverse limb deficiency -- hemangioma N/A N/A No information
Angiotensin/rennin/aldosterone hypertension N/A N/A No information
Acute hemorrhagic leukoencephalitis N/A N/A No information
Congenital cardiovascular malformations N/A N/A No information
Abdominal Aneurysm N/A N/A No information
Cardiomegaly N/A N/A No information
Binswanger's Disease N/A N/A rare
Aneurysm, intracranial berry, 8 N/A N/A No information
Blepharoptosis -- aortic anomaly N/A N/A No information
Anotia -- facial palsy -- cardiac defect N/A N/A No information
Conotruncal heart malformations N/A N/A No information
Chaotic atrial tachycardia N/A N/A No information
Bidirectional tachycardia N/A N/A No information
Double tachycardia induced by catecholamines N/A N/A No information
Capillary leak syndrome with monoclonal gammopathy N/A N/A No information
Chronic constrictive pericarditis N/A N/A No information
Viral vasculitis not HBV and HCV N/A N/A No information
Familial Tetralogy of Fallot and Glaucoma N/A N/A No information
Vascular malformations of the brain N/A N/A No information
Retinopathy, arteriosclerotic N/A N/A No information
Short QT syndrome approx 1 in 9,066,667 or 0.00% or 29 people in USA 29 less than 30 cases of short QT syndrome have been reported, Genetics Home Reference website
Inherited Hemolytic-Uremic Syndrome N/A N/A No information
Sinus node disease and myopia N/A N/A No information
Natal teeth, intestinal pseudoobstruction and patent ductus N/A N/A No information
Natal teeth intestinal pseudoobstruction patent ductus N/A N/A No information
Rheumatic heart disease N/A N/A No information
Sick sinus syndrome N/A N/A No information
Sinus node disease N/A N/A No information
Stokes Adams syndrome N/A N/A No information
Wolf-Parkinson-White syndrome approx 1 in 1,000 or 0.10% or 272,000 people in USA 272,000 1-3 per 1,000 people suffer from Wolff-Parkinson-White syndrome worldwide, Genetics Home Reference website
Tachycardia approx 1 in 62 or 1.60% or 4.4 million people in USA 4,352,000 16 per 1000 (NHIS95)
AAA N/A N/A No information
Patent ductus arteriosus N/A N/A No information
HOCM N/A N/A No information
Leukocytoclastic angiitis -- systemic N/A N/A No information
Lymphocytic vasculitis N/A N/A No information
Aerotitis syndrome N/A N/A No information
Varix N/A N/A No information
Pseudotumor Cerebri approx 1 in 272,000,000 or 0.00% or 1 people in USA 1 about 1-2 people per 100,000 population have benign intracranial hypertension in the US (Association for Spina Bifida and Hydrocephalus)
Hemangioendothelioma N/A N/A No information
Angiosarcoma of the scalp N/A N/A No information
Mitral valve prolapse, familial, X-linked N/A N/A No information
Mitral valve prolapse syndrome N/A N/A No information
Congenital mitral malformation N/A N/A No information
Mitral atresia N/A N/A No information
Mitral valve prolapse, myxomatous 1 N/A N/A No information
Mitral valve prolapse, myxomatous 2 N/A N/A No information
Arteriosclerosis Obliterans N/A N/A No information
Mitral valve prolapse, myxomatous 3 N/A N/A No information
Brugada syndrome 1 N/A N/A No information
Brugada syndrome 2 N/A N/A No information
Brugada syndrome 3 N/A N/A No information
Brugada syndrome 4 N/A N/A No information
Aneurysm of sinus of Valsalva N/A N/A No information
Hemangiopericytoma N/A N/A No information
Pierre Robin sequence -- congenital heart defect -- talipes N/A N/A No information
Tricuspid atresia N/A N/A No information
Aneurysm, Dissecting N/A N/A No information
Hyperemia N/A N/A No information
Carotid Paraganglioma N/A N/A No information
Paraganglioma N/A N/A No information
Medial Medullary Syndrome N/A N/A No information
Thrombotic thrombocytopenic purpura, congenital N/A N/A No information
Purpura simplex N/A N/A No information
Senile purpura N/A N/A No information
Thrombotic thrombocytopenic purpura, acquired approx 1 in 68 or 1.47% or 4 million people in USA 3,999,999 estimated 4-7 million people are diagnosed with thrombotic thrombocytopenic purpura each year in the US, Genetics Home Reference website
Henoch-Schonlein purpura N/A N/A No information
Angiopathy, hereditary, with nephropathy, aneurysms and muscle cramps N/A N/A No information
Renal hypertension N/A N/A No information
Renal nutcracker syndrome N/A N/A No information
Hypertrophic subaortic stenosis N/A N/A No information
Arterial dissection -- lentiginosis N/A N/A No information
Dursun Syndrome N/A N/A No information
Apparent mineralocorticoid excess N/A N/A No information
Pulmonary artery coming from the aorta N/A N/A No information
Hemangioma, capillary infantile N/A N/A No information
Right pulmonary artery, anomalous origin of, familial N/A N/A No information
Obliterative portal venopathy N/A N/A No information
Spinal AVM N/A N/A No information
Supravalvular aortic stenosis N/A N/A No information
Incessant infant ventricular tachycardia N/A N/A No information
Colobomata unilobar lung heart defect N/A N/A No information
Apparent Mineralocorticoid Excess, type 2 N/A N/A No information
Ramos-Arroyo Syndrome N/A N/A No information
Systemic Capillary Leak Syndrome N/A N/A No information
Retinal cavernous hemangioma N/A N/A No information
Pulmonary veins stenosis N/A N/A No information
Superior mesenteric artery syndrome N/A N/A No information
His bundle tachycardia N/A N/A No information
Retinal Vein Occlusion N/A N/A No information
Orthostatic intolerance N/A N/A No information
Aortic dilatation- joint hypermobility- arterial tortuosity N/A N/A No information
Anophthalmia -- heart and pulmonary anomalies -- intellectual deficit N/A N/A No information
Craniostenosis with congenital heart disease mental retardation N/A N/A No information
Double outlet -- right ventricle I N/A N/A No information
Thoracic outlet syndrome TOS N/A N/A No information
Double outlet right ventricle N/A N/A No information
Thoracic outlet syndrome N/A N/A No information
Double outlet -- right ventricle II N/A N/A No information
Double outlet -- right ventricle IV N/A N/A No information
Double outlet -- left ventricle N/A N/A No information
Brain malformation -- congenital heart disease -- postaxial polydactyly N/A N/A No information
Chronic necrotizing vasculitis N/A N/A No information
Cleft palate -- heart disease -- polydactyly -- absent tibia N/A N/A No information
Phocomelia ectrodactyly deafness sinus arrhythmia N/A N/A No information
Phocomelia ectrodactyly ear malformation deafness sinus arrhythmia N/A N/A No information
Polysyndactyly -- cardiac malformation N/A N/A No information
Heart defect, tongue hamartoma and polysyndactyly N/A N/A No information
Frontonasal dysplasia -- phocomelic upper limbs N/A N/A No information
Pulmonary atresia with ventricular septal defect N/A N/A No information
Aortic arches defect N/A N/A No information
Arterial occlusive disease, progressive -- hypertension -- heart defects -- bone fragility -- brachysyndactyly N/A N/A No information
Pulmonary atresia -- intact ventricular septum N/A N/A No information
Duodenal atresia tetralogy of Fallot N/A N/A No information
Duodenojejunal atresia with volvulus, absent dorsal mesentery and absent superior mesenteric artery N/A N/A No information
Arterial calcification of infancy N/A N/A No information
Dextrocardia N/A N/A No information
Meningeal angiomatosis -- cleft hypoplastic left heart N/A N/A No information
Choanal atresia -- deafness -- cardiac defects -- dysmorphism N/A N/A No information
Vascular malposition N/A N/A No information
Bone infarct N/A N/A No information
Amyloid angiopathy N/A N/A No information
Amyloid cardiopathy, familial N/A N/A No information
Ellis-van Creveld syndrome approx 1 in 60,000 or 0.00% or 4,533 people in USA 4,533 1 per 60,000 - 200,000 newborns are affected by Ellis-van Creveld syndrome worldwide, Genetics Home Reference website
Chondroectodermal dysplasia N/A N/A No information
Coarctation of aorta dominant N/A N/A No information
Benign angiitis of the central nervous system N/A N/A No information
Arterial tortuosity syndrome N/A N/A No information
Acute peripheral arterial occlusion N/A N/A No information
Skeletal and Cardiac Malformations with thrombocytopenia N/A N/A No information
Skeleto cardiac syndrome with thrombocytopenia N/A N/A No information
Pigmented purpuric eruption N/A N/A No information
Environment associated hypertension N/A N/A No information
Hemangiomatosis, familial pulmonary capillary N/A N/A No information
Angioma serpiginosum N/A N/A No information
Tufted angioma N/A N/A No information
Cardiac diverticulum N/A N/A No information
Single ventricular heart N/A N/A No information
Distichiasis -- heart and vasculature anomalies N/A N/A No information
Angioma hereditary neurocutaneous N/A N/A No information
Hemolytic uremic syndrome N/A N/A No information
Hemolytic uremic syndrome, atypical, childhood N/A N/A No information
D-minus hemolytic uremic syndrome (D-HUS) -- pregnancy related N/A N/A No information
D-plus hemolytic uremic syndrome (D+HUS) N/A N/A No information
Atypical hemolytic uremic syndrome N/A N/A No information
D-minus hemolytic uremic syndrome (D-HUS) -- familial N/A N/A No information
Bicuspid aortic valve N/A N/A No information
Conn Syndrome-induced hypertension N/A N/A No information
Erythropoietin-induced hypertension N/A N/A No information
Carotid bruits N/A N/A No information
Fetal left ventricular aneurysm N/A N/A No information
Jugular lymphatic obstruction sequence N/A N/A No information
Idiopathic pulmonary hypertension N/A N/A No information
Cavernous hemangioma N/A N/A No information
Cutaneous necrotizing vasculitis N/A N/A No information
Truncus Arteriosus N/A N/A No information
Persistent Truncus Arteriosus N/A N/A No information
Arterial dissections with lentiginosis N/A N/A No information
Non-diarrheal (D-) HUS syndrome N/A N/A No information
Intracranial arteriovenous malformation N/A N/A No information
Pulmonary arterio-veinous aneurysm N/A N/A No information
Persistent patency of the arterial duct N/A N/A No information
Angiokeratoma N/A N/A No information
Twisted atrioventricular connections N/A N/A No information
Pulmonary artery, isolated unilateral absence of (Isolated UAPA) N/A N/A No information
Portal hypertension due to intrahepatic block N/A N/A No information
Internal carotid agenesis N/A N/A No information
Cystic medial necrosis of aorta N/A N/A No information
Congenital heart disease, ptosis, hypodontia, craniosynostosis N/A N/A No information
Tabatznik syndrome N/A N/A No information
Colobomatous microphthalmia -- heart disease -- hearing loss N/A N/A No information
Cutaneous vascularitis N/A N/A No information
Juvenile temporal arteritis N/A N/A No information
Partial atrioventricular canal N/A N/A No information
Parkes-Weber syndrome I N/A N/A No information
Rheumatoid vasculitis N/A N/A No information
Acrocephaly -- pulmonary stenosis -- mental retardation N/A N/A No information
Atrial myxoma, familial N/A N/A No information
Transposition of great arteries N/A N/A No information
Kidney arteriovenous fistula N/A N/A No information
Unusual facies, preauricular pits, fifth finger clinodactyly and tetralogy of Fallot N/A N/A No information
Hemorrhagic shock and encephalopathy syndrome N/A N/A No information
Endomyocardial fibrosis N/A N/A No information
Multiple system atrophy (MSA) with orthostatic hypotension N/A N/A No information
Periodic paralysis, potassium-sensitive, cardiodysrythmic type N/A N/A No information
Short stature webbed neck heart disease N/A N/A No information
Pulmonary branches stenosis N/A N/A No information
Monakow syndrome N/A N/A No information
Congenital arteriovenous shunt N/A N/A No information
Cardiac malformation N/A N/A No information
Anterior spinal artery stroke N/A N/A No information
Congenital aneurysms of the great vessels N/A N/A No information
Anterior cord syndrome N/A N/A No information
Anterior spinal artery syndrome N/A N/A No information
HERNS syndrome N/A N/A No information
Gram's syndrome N/A N/A No information
Loeffler's endocarditis N/A N/A No information
Atrial tachyarrhythmia with short pr interval N/A N/A No information
Mungan syndrome N/A N/A No information
Osteoradionecrosis N/A N/A No information
Superior vena cava syndrome N/A N/A No information
Hemangioma thrombocytopenia syndrome N/A N/A No information
Pulmonary hemangiomatosis N/A N/A No information
Brachydactyly, mesomelia, mental retardation, aortic dilation, mitral valve prolapse and characteristic face N/A N/A No information
Hereditary vascular retinopathie -- Raynaud phenomenon -- migraine N/A N/A No information
Aorta-pulmonary artery fistula N/A N/A No information
Hydrocephaly low insertion umbilicus N/A N/A No information
Angiotensin renin aldosterone hypertension N/A N/A No information
Cranio-facio-cardio-skeletal dysplasia N/A N/A No information
Houlston ironton temple syndrome de N/A N/A No information
Vertebral Artery Dissection N/A N/A No information
Lymphoedema -- cerebral arteriovenous anomaly N/A N/A No information
Obesity -- colitis -- hypothyroidism -- cardiac hypertrophy -- developmental delay N/A N/A No information
Moyamoya Disease N/A N/A rare
Polyarteritis nodosa N/A N/A No information
Shy-Drager Syndrome N/A N/A No information
Sturge-Weber Syndrome N/A N/A No information
Wallenberg's Syndrome N/A N/A No information
Williams Syndrome approx 1 in 7,500 or 0.01% or 36,266 people in USA 36,266 estimated 1 per 7,500 - 20,000 people suffer from Williams syndrome, Genetics Home Reference website
Buerger's disease N/A N/A No information
Superficial thrombophlebitis N/A N/A No information
Osteochondritis Dissecans N/A N/A No information
Peripheral vascular disease N/A N/A No information
Congestive cardiac failure N/A N/A No information
CCF N/A N/A No information
Ischemia N/A N/A No information
Aortic dissection N/A N/A No information
Compartment Syndrome N/A N/A No information
Patent foramen ovale N/A N/A No information
HELLP syndrome N/A N/A No information
Cadasil approx 1 in 15,000,000 or 0.00% or 18 people in USA 18 about 400 people have been diagnosed with CADASIL worldwide, Genetics Home Reference website
Moyamoya Syndrome N/A N/A No information
Ivemark Syndrome N/A N/A No information
Isthmus coarctation N/A N/A No information
Eisenmenger Syndrome N/A N/A No information
Churg-Strauss Syndrome N/A N/A No information
Twin-Twin Transfusion Syndrome N/A N/A No information
Singleton-Merten Syndrome N/A N/A No information
Coats Disease N/A N/A No information
Eales Disease N/A N/A No information
Cor Triatriatum N/A N/A No information
Pentalogy of Cantrell N/A N/A No information
Brugada Syndrome approx 1 in 2,000 or 0.05% or 136,000 people in USA 136,000 estimated 5 per 10,000 people suffer from Brugada syndrome worldwide, Genetic Home Reference website
Idiopathic, hypertrophic, subaortic stenosis N/A N/A No information
Cutis Marmorata Telangiectatica Congenita N/A N/A No information
Degos Disease N/A N/A No information
Lymphomatoid Granulomatosis N/A N/A No information
LEOPARD Syndrome N/A N/A No information
Jervell and Lange-Nielsen Syndrome approx 1 in 200,000 or 0.00% or 1,360 people in USA 1,360 at least 1 per 200,00 people suffer from Jervell and Lange-Nielsen syndrome in Denmark, Genetics Home Reference website
Acardia N/A N/A No information
Banti's syndrome N/A N/A No information
Microscopic Polyangiitis N/A N/A No information
Sheehan Syndrome N/A N/A No information
Cardiofaciocutaneous Syndrome N/A N/A No information
CHARGE Syndrome N/A N/A No information
Banti Syndrome N/A N/A No information
Laurence-Moon Syndrome N/A N/A No information
Nonhypertension syndrome N/A N/A No information
Thalamic Syndrome (Dejerine Roussy) N/A N/A No information
Small cuff syndrome N/A N/A No information
Gronblad-Strandberg-Touraine syndrome N/A N/A No information
Ruvalcaba Churesigaew Myhre syndrome N/A N/A No information
Borud Syndrome N/A N/A No information
Cornel syndrome N/A N/A No information
Koroxenidis Syndrome N/A N/A No information
Camera Costa Syndrome N/A N/A No information
Stoll Levy Francort Syndrome N/A N/A No information
Intellectual deficit -- multiple anomalies N/A N/A No information
Claudication pain N/A N/A No information
Mac Duffie's syndrome N/A N/A No information
Human HOXA1 Syndromes N/A N/A No information
Limited cutaneous systemic sclerosis N/A N/A No information
Aortic supravalvular stenosis N/A N/A No information
Dextrocardia with situs inversus N/A N/A No information
Borrone-Di Rocco-Crovato syndrome N/A N/A No information
Cutaneomeningospinal angiomatosis N/A N/A No information
Dermato-cardio-skeletal syndrome Borrone type N/A N/A No information
Grange syndrome N/A N/A No information
Leriche's Syndrome N/A N/A No information
Levocardia N/A N/A No information
Schroeder syndrome 1 N/A N/A No information
Supine hypotensive syndrome N/A N/A No information
Wagener syndrome N/A N/A No information
Zanoli-Vecchi syndrome N/A N/A No information
Angio-osteohypotrophic syndrome N/A N/A No information
Vater-like syndrome, with pulmonary hypertension, abnormal ears and growth deficiency N/A N/A No information
Bosley-Salih-Alorainy syndrome N/A N/A No information
Heller-Dohle disease N/A N/A No information
Hilger syndrome N/A N/A No information
Hoigne syndrome N/A N/A No information
Kreibig opticomalacia N/A N/A No information
Kugel-Stoloff syndrome N/A N/A No information
Leriche syndrome N/A N/A No information
Majocchi disease N/A N/A No information
Moynahan syndrome I N/A N/A No information
Nicolau syndrome N/A N/A No information
Dressler syndrome N/A N/A No information
Pott gangrene N/A N/A No information
REST syndrome N/A N/A No information
Viscero-atrial heterotaxia N/A N/A No information
Hypocomplementemic urticarial vasculitis N/A N/A No information
Richieri-Costa-Orquizas syndrome N/A N/A No information
Fibrocartilaginous embolism N/A N/A No information
Alveolar capillary dysplasia N/A N/A No information
Hunter-Mcdonald syndrome N/A N/A No information
Ho Kaufman-Mcalister syndrome N/A N/A No information
Lipodermatosclerosis N/A N/A No information
Kallikrein hypertension N/A N/A No information
Left ventricle-aorta tunnel N/A N/A No information
Bindewald-Ulmer-Muller syndrome N/A N/A No information
Coffin syndrome 1 N/A N/A No information
Hordnes-Engebretsen-Knudtson syndrome N/A N/A No information
Dieterich's disease N/A N/A No information
Cor biloculare N/A N/A No information
Idaho syndrome N/A N/A No information
Pulmonary venous return anomaly N/A N/A No information
Cardiac valvular dysplasia, X-linked N/A N/A No information
Catecholamine hypertension N/A N/A No information
Boscherini-Galasso-Manca-Bitti syndrome N/A N/A No information
Lemierre's syndrome N/A N/A No information
Angiomyomatous Hamartoma N/A N/A No information
Burn-McKeown syndrome N/A N/A No information
Hurst-Hallam-Hockey syndrome N/A N/A No information
Cardioauditory syndrome of Sanchez- Cascos N/A N/A No information
Kozlowski-Celermajer syndrome N/A N/A No information
Laurence-Prosser-Rocker syndrome N/A N/A No information
Hypertelorism and tetralogy of Fallot N/A N/A No information
Celiac artery stenosis from compression by median arcuate ligament of diaphragm N/A N/A No information
Amniotic fluid syndrome N/A N/A No information
Basilar artery insufficiency syndrome N/A N/A No information
Beau's syndrome N/A N/A No information
Bernheim's syndrome N/A N/A No information
Bing-Neel syndrome N/A N/A No information
Bland-Garland-White syndrome N/A N/A No information
Bouillaud's syndrome N/A N/A No information
Cast syndrome N/A N/A No information
Bartschi-Rochaix syndrome N/A N/A No information
Beck's triad N/A N/A No information
Cardiac tamponade N/A N/A No information
Bernheim syndrome N/A N/A No information
Bland-White -Garland syndrome N/A N/A No information
Bluefarb-Stewart syndrome N/A N/A No information
Bone cement implantation syndrome N/A N/A No information
Bradbury-Eggleston syndrome N/A N/A No information
Da Costa syndrome N/A N/A No information
Discontinuation syndrome N/A N/A No information
Favre-Chaix angiodermatitis N/A N/A No information
Foix-Alajouanine syndrome N/A N/A No information
MoyaMoya disease 1 N/A N/A No information
Shwartzman phenomenon N/A N/A No information
Ruvalcaba-Churesigaew-Myhre syndrom N/A N/A No information
Orstavik-Lindemann-Solberg syndrome N/A N/A No information
Renoprival hypertension N/A N/A No information
Subpulmonary stenosis N/A N/A No information
Humerospinal dysostosis -- congenital heart disease N/A N/A No information
Sener syndrome N/A N/A No information
Marfan-like syndrome, Boileau type N/A N/A No information
Granulomatous Angiitis of the Central Nervous System N/A N/A No information
MoyaMoya disease 2 N/A N/A No information
MoyaMoya disease 3 N/A N/A No information
Multifocal ventricular premature beats N/A N/A No information
Reynolds-Neri-Hermann syndrome N/A N/A No information
Naxos disease N/A N/A No information
Megalencephaly -- cutis marmorata telangiectatica congenita N/A N/A No information
Nathalie syndrome N/A N/A No information
Diffuse neonatal hemangiomatosis N/A N/A No information
Endomyocardial fibroelastosis N/A N/A No information
Fraser-like syndrome N/A N/A No information
Feigenbaum-Bergeron-Richardson syndrome N/A N/A No information
Malouf syndrome N/A N/A No information
Sonoda syndrome N/A N/A No information
Sacral hemangiomas -- multiple congenital abnormalities N/A N/A No information
Thomas syndrome N/A N/A No information
Gay-Feinmesser-Cohen syndrome N/A N/A No information
Polymorphic catecholergic ventricular tachycardia N/A N/A No information
Montefiore syndrome N/A N/A No information
Lowry-Maclean syndrome N/A N/A No information
Subaortic stenosis -- short stature syndrome N/A N/A No information
Axial mesodermal dysplasia spectrum N/A N/A No information
Sternal cyst -- vascular anomalies N/A N/A No information
Manouvrier syndrome N/A N/A No information
Shoulder and thorax deformity, congenital heart disease N/A N/A No information
Loeys-Dietz syndrome N/A N/A No information
Dandy-Walker -- facial hemangioma N/A N/A No information
Dermatocardioskeletal syndrome, Boronne type N/A N/A No information
Rambaud-Galian syndrome N/A N/A No information
HEC syndrome N/A N/A No information
D ercole syndrome N/A N/A No information
Steinfeld syndrome N/A N/A No information
Pulmonary supravalvular stenosis N/A N/A No information
Palmer-Pagon syndrome N/A N/A No information
Complete atrioventricular canal N/A N/A No information
Irons-Bhan syndrome N/A N/A No information
Susac syndrome N/A N/A No information
Kasznica-Carlson-Coppedge syndrome N/A N/A No information
Aughton syndrome N/A N/A No information
Familial venous malformations N/A N/A No information
McGillivray syndrome N/A N/A No information
Smith-Martin-Dodd syndrome N/A N/A No information
Colver-Steer-Godman syndrome N/A N/A No information
Tako-Tsubo syndrome N/A N/A No information
Kennerknecht-Sorgo-Oberhoffer syndrome N/A N/A No information
Timothy syndrome N/A N/A No information
Ellis-Yale-Winter syndrome N/A N/A No information
Pulmonary veno-occlusive disease N/A N/A No information
Rhabdomyomatous dysplasia -- cardiopathy -- genital anomalies N/A N/A No information
Okamuto Satomura syndrome N/A N/A No information
Mondor's disease N/A N/A No information
Char syndrome N/A N/A No information
Reactive angioendotheliomatosis N/A N/A No information
MASS syndrome N/A N/A No information
Idiopathic dilatation of the pulmonary artery N/A N/A No information
Taussig Bing syndrome N/A N/A No information
Storm syndrome N/A N/A No information
Angiomatosis, diffuse corticomeningeal, of Divry and Van Bogaert N/A N/A No information
Holzgreve-Wagner-Rehder syndrome N/A N/A No information
Rowley-Rosenberg syndrome N/A N/A No information
Lenegre disease N/A N/A No information
Adams Nance syndrome N/A N/A No information
Al Gazali Aziz Salem syndrome N/A N/A No information
Beemer-Ertbruggen syndrome N/A N/A No information
Avasthey syndrome N/A N/A No information
Grand-Kaine-Fulling syndrome N/A N/A No information
Kashani-Strom-Utley syndrome N/A N/A No information
Rommen-Mueller-Sybert syndrome N/A N/A No information
Levotransposition of the great arteries N/A N/A No information
PHACE association N/A N/A No information
Cranioacrofacial syndrome N/A N/A No information
Coronaro-cardiac fistula N/A N/A No information
Faciocardiorenal syndrome N/A N/A No information
Jeune-Tommasi syndrome N/A N/A No information
Cote-Katsantoni syndrome N/A N/A No information
Thurman-Hillier syndrome N/A N/A No information
Lujan-Fryns syndrome N/A N/A No information
Ramos-ArroyoClark syndrome N/A N/A No information
Forney Robinson Pascoe syndrome N/A N/A No information
Keshan disease N/A N/A No information
Ivemark II N/A N/A No information
Calciphylaxis N/A N/A No information
Ebstein's anomaly N/A N/A No information
Ductus arteriosus, patent reversed flow N/A N/A No information
Meadows syndrome N/A N/A No information
McKusick-Kaufman syndrome N/A N/A No information
Watson syndrome N/A N/A No information
Mesenteric artery syndrome N/A N/A No information
Endocardial fibroelastosis N/A N/A No information
Blue rubber bleb nevus N/A N/A No information
Perniosis N/A N/A No information
Sneddon Syndrome N/A N/A No information
Takayasu arteritis N/A N/A No information
Andersen-Tawil syndrome approx 1 in 60,000,000 or 0.00% or 4 people in USA 4 100 people have been reported with Andersen-Tawil syndrome worldwide, Genetics Home Reference
Waterhouse-Friederichsen syndrome N/A N/A No information
Gaucher-like disease N/A N/A only a few cases of Gaucher-like disease have been reported worldwide, Genetics Home Reference website
Wilkie Taylor Scambler syndrome N/A N/A No information
Verloove Vanhorick Brubakk syndrome N/A N/A No information
Watermelon stomach N/A N/A No information
Zunich neuroectodermal syndrome N/A N/A No information
Winship Viljoen Leary syndrome N/A N/A No information
Dahlberg syndrome N/A N/A No information
Shaver's disease N/A N/A No information
Pulmonary arteriovenous fistula N/A N/A No information
Lewis (F.) syndrome N/A N/A No information
Keutel syndrome N/A N/A No information
Foix-Chavany-Marie syndrome N/A N/A No information
Hereditary hemorrhagic telangiectasia approx 1 in 5,000 or 0.02% or 54,400 people in USA 54,399 estimated 1 per 5,000 - 10,000 people suffer from hereditary hemorrhagic telangiectasia worldwide, Genetics Home Reference website
Limb-body wall complex N/A N/A No information
CHILD syndrome ichthyosis N/A N/A No information
Van der Woude syndrome 2 N/A N/A No information
Uhl anomaly N/A N/A No information
Ausrian triad N/A N/A No information
Ventricular familial preexcitation syndrome N/A N/A No information
Vasculitis, cutaneous necrotising N/A N/A No information
Vasculitis hypersensitivity N/A N/A No information
Vein of Galen aneurysm N/A N/A No information
Valvular dysplasia of the child N/A N/A No information
Van Allen Myhre syndrome N/A N/A No information
Ventricular extrasystoles perodactyly Robin sequence N/A N/A No information
Budd-Chiari syndrome N/A N/A No information
NAME syndrome N/A N/A No information
Cayler syndrome N/A N/A No information
Fallot syndrome N/A N/A No information
Leber miliary aneurysm N/A N/A No information
Baetz-Greenwalt syndrome N/A N/A No information
Romano-Ward syndrome approx 1 in 7,000 or 0.01% or 38,857 people in USA 38,857 estimated 1 per 7,000 people suffer from Romano-Ward syndrome worldwide, Genetics Home Reference website

Types of Circulatory system conditions

For more information about types of Circulatory system conditions, refer to our section on types of Circulatory system conditions.

About prevalence:

The medical term 'prevalence' of Circulatory system conditions usually refers to the estimated population of people who are managing Circulatory system conditions at any given time, whereas the annual diagnosis rate of new cases of Circulatory system conditions is called the 'incidence'. For more information on prevalence and incidence statistics, see about prevalence and incidence statistics.

 

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