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Symptoms » Artery symptoms » Glossary
 

Glossary for Artery symptoms

Medical terms related to Artery symptoms or mentioned in this section include:

  • Abdominal symptoms: Symptoms affecting the abdomen or digestive tract
  • Aneurysm: Swelling or ballooning of part of an artery
  • Aneurysms: An area of dilation of the wall of an artery or vein
  • Angiopathy, hereditary, with nephropathy, aneurysms and muscle cramps: An inherited disorder characterized by kidney disease, aneurysms, blood vessel disease and muscle cramps which can last from seconds to minutes.
  • Antiphospholipid syndrome: An autoimmune disorder characterized by blood clots and pregnancy losses.
  • Apo A-I deficiency: Low plasma HDL cholesterol that tends to run in families.
  • Arterial dissection -- lentiginosis: A rare inherited condition characterized by arterial dissection and numerous skin macules. An arterial dissection is a blood vessel anomaly where blood leaks into the blood vessel wall through a tear in the inner lining of the blood vessel.
  • Arterial dissections with lentiginosis: A rare familial syndrome characterized by the association of aortic dissection and multiple lentigines (brown skin spots). The aorta can rupture in some cases and result in sudden death.
  • Arterial hypertension: medical condition in which the blood pressure is chronically elevated.
  • Arteriosclerosis: A group of medical conditions which are characterized by the thickening and loss of elasticity of arterial blood vessel walls
  • Artery conditions: Any conditions affecting arteries
  • Atherosclerosis: A condition which is a form of arteriosclerosis where atheromas are caused by the aggregation of cholesterol and lipids
  • Autosomal dominant polycystic kidney disease: Genetic kidney disease causing kidney cysts.
  • Behcet's syndrome: Recurring inflammation of small blood vessels affecting various areas.
  • Binswanger Disease: Multi-infarct dementia, caused by damage to deep white matter.
  • Binswanger's Disease: A type of senile dementia characterized by chronic cerebrovascular disease.
  • Blood vessel conditions: Conditions that affect the blood vessels
  • Blood vessel symptoms: Symptoms affecting the blood vessels
  • Carbon disulfide-induced cardiovascular disease: Chronic exposure to certain chemicals can cause cardiovascular disease. For example, exposure to Carbon disulfide can lead to heart disease and carries a risk of premature death as a result. Chronic exposure to these sort of chemicals is most likely to occur in a work environment. Carbon disulfide is used mainly in viscose rayon manufacturing but is also used as a solvent and in other process. Exposure usually occurs through inhalation of vapours but skin absorption can also occur. Reported cases haf cardiovascular disease has occurred among workers exposed to carbon disulfide concentrations of 20-60 ppm.
  • Cardiotoxicity -- Allylamine: Exposure to Allylamines can have a toxic effect on the heart and may result in degenerative changes in the heart. The degree of toxicity may be influenced the duration and level of exposure to the chemical.
  • Cardiotoxicity -- Aromatic hydrocarbons: Exposure to Aromatic hydrocarbons can have a toxic effect on the heart and may result in degenerative changes in the heart. The degree of toxicity may be influenced the duration and level of exposure to the chemical.
  • Cardiotoxicity -- Carbon Disulfide: Exposure to Carbon Disulfide can have a toxic effect on the heart and may result in degenerative changes in the heart. The degree of toxicity may be influenced the duration and level of exposure to the chemical.
  • Cardiotoxicity -- Carbon Monoxide: Exposure to Carbon Monoxide can have a toxic effect on the heart and may result in degenerative changes in the heart. The degree of toxicity may be influenced the duration and level of exposure to the chemical.
  • Cerebrovascular symptoms: Symptoms related to the brain's arteries
  • Chagas Cardiomyopathy: Heart disease that can occur as a complication of a chronic parasitic infection caused by the protozoa Trypanosoma cruzi and transmitted by insect bites or blood transfusions.
  • Chemical-induced cardiovascular disease: Chronic exposure to certain chemicals can cause cardiovascular disease. For example, exposure to Carbon disulfide can lead to heart disease and carries a risk of premature death as a result. Chronic exposure to these sort of chemicals is most likely to occur in a work environment.
  • Cholesterol and lipids: Levels of blood or urine cholesterol or lipids as a symptom
  • Circulation symptoms: Symptoms affecting the circulatory system
  • Cyanosis: Blueness or purple coloring of skin.
  • Distichiasis -- heart and vasculature anomalies: A rare birth syndrome characterized by heart and blood vessel abnormalities as well as the growth of an extra row of eyelashes.
  • Ehlers Danlos syndrome type 4, autosomal dominant: A rare genetic connective tissue disorder characterized by delicate skin, fragile blood vessels, distinctive facial features and minimal joint problems - previously known as EDS type 4.
  • Ehlers-Danlos syndrome type IV: A rare genetic connective tissue disorder characterized by small joint hypermobility, easy bruising and characteristic facial appearance - a vascular or ecchymotic form of the condition.
  • Ehlers-Danlos syndrome type VI: A rare genetic connective tissue disorder characterized by lax joints, scoliosis and fragile sclera of the eye - Ehlers Danlos type with predominant ocular abnormalities.
  • Ehlers-Danlos syndrome, 6B: A rare genetic connective tissue disorder characterized by lax joints, scoliosis and fragile sclera of the eye - Ehlers Danlos type with predominant ocular abnormalities but lysyl-hydroxylase activity is normal1.
  • Ehlers-Danlos syndrome, kyphoscoliosis type: A rare genetic connective tissue disorder caused by deficiency of the lysyl hydroxylase enzyme and is characterized by progressive scoliosis and muscle weakness and fragile sclera - previously known as EDS type 6.
  • Ehlers-Danlos syndrome, vascular type: A rare genetic connective tissue disorder characterized by delicate skin, fragile blood vessels, distinctive facial features and minimal joint problems - previously known as EDS type 4.
  • Fabry disease: Genetic fat storage disorder
  • Familial Hypercholesterolemia: A genetic abnormality which causes patients to have abnormally high cholesterol levels (low-density lipoproteins). The condition usually leads to early cardiovascular disease.
  • Fibromuscular dysplasia of arteries: A rare disease where the blood vessel walls thicken and harden which reduces blood flow through the arteries and into various organs. The main arteries that may be affected are those in the kidney's and abdomen as well as the carotid artery which caries blood from the heart to the neck.
  • Head symptoms: Symptoms affecting the head or brain
  • High Blood Pressure/Hypertension:
  • High blood pressure: Excessive blood pressure.
  • Hutchinson Gilford Syndrome: A rare genetic disorder characterized by alopecia and senile-like appearance.
  • Hypercholesterolemia due to LDL receptor deficiency: A disorder involving a defect in the protein (LDL receptor) that allows cholesterol to be transported to where it can be used means that it builds up in the blood and blood vessels where it can cause problems.
  • Hypercholesterolemia due to arg3500 mutation of Apo B-100: A rare disorder where a defect in the protein that transports cholesterol (apolipoprotein B-100) means that it builds up in the blood and blood vessels where it can cause problems.
  • Hypercholesterolemia, autosomal dominant: A dominantly inherited disorder of cholesterol metabolism which causes premature coronary artery disease.
  • Hyperhomocysteinemia: Excessive homocysteine levels in blood. It is often associated with folate or cobalamin deficiency as well as genetic defects. Severity of symptoms is determined by how high the homocysteine levels are. Sufferers are generally asymptomatic until the onset of premature arterial disease later in life. Other symptoms such as mental retardation only occur in severe cases where the homocysteine levels are extremely high.
  • Hypertension, Essential: Essential hypertension is a type of hypertension that has no detectable cause. Patients have an increased blood pressure for no apparent reason. Most cases of hypertension are of this form.
  • Hypertension, Essential, Susceptibility to: Essential hypertension is a type of hypertension that has no detectable cause. Patients have an increased blood pressure for no apparent reason. Most cases of hypertension are of this form. Researchers have identified a number of genes linked to an increased susceptibility of developing hypertension.
  • Hypertension, Essential, Susceptibility to, 1: Essential hypertension is a type of hypertension that has no detectable cause. Patients have an increased blood pressure for no apparent reason. Most cases of hypertension are of this form. Researchers have identified a number of genes linked to an increased susceptibility of developing hypertension. Type 1 is linked to a defect on chromosome 17q.
  • Hypertension, Essential, Susceptibility to, 2: Essential hypertension is a type of hypertension that has no detectable cause. Patients have an increased blood pressure for no apparent reason. Most cases of hypertension are of this form. Researchers have identified a number of genes linked to an increased susceptibility of developing hypertension. Type 2 is linked to a defect on chromosome 15q.
  • Hypertension, Essential, Susceptibility to, 3: Essential hypertension is a type of hypertension that has no detectable cause. Patients have an increased blood pressure for no apparent reason. Most cases of hypertension are of this form. Researchers have identified a number of genes linked to an increased susceptibility of developing hypertension. Type 3 is linked to a defect on chromosome 2p25-p24.
  • Hypertension, Essential, Susceptibility to, 4: Essential hypertension is a type of hypertension that has no detectable cause. Patients have an increased blood pressure for no apparent reason. Most cases of hypertension are of this form. Researchers have identified a number of genes linked to an increased susceptibility of developing hypertension. Type 4 is linked to a defect on chromosome 12p12.2-p12.1.
  • Hypertension, Essential, Susceptibility to, 5: Essential hypertension is a type of hypertension that has no detectable cause. Patients have an increased blood pressure for no apparent reason. Most cases of hypertension are of this form. Researchers have identified a number of genes linked to an increased susceptibility of developing hypertension. Type 5 is linked to a defect on chromosome 20q11-q13.
  • Hypertension, Essential, Susceptibility to, 6: Essential hypertension is a type of hypertension that has no detectable cause. Patients have an increased blood pressure for no apparent reason. Most cases of hypertension are of this form. Researchers have identified a number of genes linked to an increased susceptibility of developing hypertension. Type 6 is linked to a defect on chromosome 5p13-q12.
  • Hypertension, Essential, Susceptibility to, 7: Essential hypertension is a type of hypertension that has no detectable cause. Patients have an increased blood pressure for no apparent reason. Most cases of hypertension are of this form. Researchers have identified a number of genes linked to an increased susceptibility of developing hypertension. Type 7 is linked to a defect on chromosome 3p14.1-q12.3.
  • Hypertension, Essential, Susceptibility to, 8: Essential hypertension is a type of hypertension that has no detectable cause. Patients have an increased blood pressure for no apparent reason. Most cases of hypertension are of this form. Researchers have identified a number of genes linked to an increased susceptibility of developing hypertension. Type 8 is linked to a defect on chromosome 18q21.2.
  • Hypoalphalipoproteinemia (generic term): Inherited low plasma HDL cholesterol level.
  • Hypoalphalipoproteinemia, primary: Low level of plasma HDL cholesterol that runs in the family.
  • Ischemia: Inadequate blood supply to tissues, usually caused by a problem in the blood vessel.
  • Kawasaki disease: A childhood illness that generally affects the skin, mouth and lymph nodes.
  • Menkes Disease: Genetic disease of copper deficiency.
  • Muscle symptoms: Symptoms affecting the muscles of the body
  • Nerve symptoms: Symptoms affecting the nerves
  • Nicolau syndrome: A rare complication resulting from the injection of a drug into an artery instead of the muscles where it was intended.
  • PHACE association: A very rare syndrome characterized mainly by a brain malformation (involving the posterior fossa), large facial hemangioma and eye, heart and artery anomalies.
  • Polyarteritis nodosa: A serious blood vessel disease where small and medium-sized arteries become swollen and damaged and are unable to adequately supply oxygenated blood to various tissues in the body. The disease can occur in a mild form or a serious, rapidly fatal form.
  • Polychondritis: A serious, progressive, episodic condition characterized by inflammation and degeneration of cartilage in the body. The duration and severity of the episodes can vary.
  • Polycystic kidney disease: Genetic kidney disease causing kidney cysts.
  • Premature aging: Early appearance of the signs of aging before old age
  • Primary hyperoxaluria type 1: A rare inherited inborn metabolic disorder characterized by excessive amounts of oxalate in the urine and deposits of oxalate in the kidneys which leads to progressive kidney failure. There are two subtypes of Oxalosis, each with a different origin for the genetic defect involved. Type 1 involves a deficiency of a liver enzyme called Alanine-glyoxylate aminotransferase. Type 2 tends to cause a milder disease than type 1 with better longterm outcomes.
  • Progeria: A rare fatal genetic disorder characterized by extremely premature aging.
  • Pseudoxanthoma elasticum, forme fruste: An inherited systemic disease of connective tissue involving progressive calcification and degeneration of elastic fibers throughout the body, including the skin, eyes and cardiovascular system.
  • Rambaud-Galian syndrome: A very rare syndrome characterized by the progressive deposition of a substance called hyaline in blood vessels of the digestive tract and kidneys. Calcification of the brain is also present.
  • Sneddon Syndrome: A rare progressive inherited disorder involving the blood vessel disease and neurological symptoms.
  • Stroke symptoms: Brain-related symptoms of bleeding or blockage.
  • Syphilis: A sexually transmitted disease caused by a bacteria (Treponema pallidum). The condition is often asymptomatic in the early stages but one or more sores may be present in the early stages. Untreated syphilis usually results in remission of visible symptoms but further severe damage may occur to internal organs and other body tissues which can result in death.
  • Systemic Lupus Erythematosus with Hemolytic Anemia, Susceptibility to, 1: Systemic Lupus Erythematosus is an autoimmune disease affecting mostly women and causing various effects throughout different parts of the body. Its severity can range from very mild to extremely serious depending on which body organs are afflicted. Researchers have discovered a number of genes linked to an increased susceptibility of developing SLE and hemolytic anemia - the anemia often occurs months or even years before symptoms of SLE develop. Type 1 is linked to a defect on chromosome 11q14.
  • Systemic Lupus Erythematosus with Nephritis, Susceptibility to, 1: Systemic Lupus Erythematosus is an autoimmune disease affecting mostly women and causing various effects throughout different parts of the body. Its severity can range from very mild to extremely serious depending on which body organs are afflicted. Researchers have discovered a number of genes linked to an increased susceptibility of developing SLE and nephritis. More than half of SLE patients will develop nephritis. Type 1 is linked to a defect on chromosome 10q22.3.
  • Systemic Lupus Erythematosus with Vitiligo, Susceptibility to, 1: Systemic Lupus Erythematosus is an autoimmune disease affecting mostly women and causing various effects throughout different parts of the body. Its severity can range from very mild to extremely serious depending on which body organs are afflicted. Researchers have discovered a number of genes linked to an increased susceptibility of developing SLE and vitiligo. Type 1 is linked to a defect on chromosome 17p13.
  • Systemic Lupus Erythematosus, Susceptibility to, 1: Systemic Lupus Erythematosus is an autoimmune disease affecting mostly women and causing various effects throughout different parts of the body. Its severity can range from very mild to extremely serious depending on which body organs are afflicted. Researchers have discovered a number of genes linked to an increased susceptibility of developing SLE. Type 1 is linked to a defect on chromosome 1q41.
  • Systemic Lupus Erythematosus, Susceptibility to, 10: Systemic Lupus Erythematosus is an autoimmune disease affecting mostly women and causing various effects throughout different parts of the body. Its severity can range from very mild to extremely serious depending on which body organs are afflicted. Researchers have discovered a number of genes linked to an increased susceptibility of developing SLE. Type 10 is linked to a defect on chromosome 7q32.
  • Systemic Lupus Erythematosus, Susceptibility to, 11: Systemic Lupus Erythematosus is an autoimmune disease affecting mostly women and causing various effects throughout different parts of the body. Its severity can range from very mild to extremely serious depending on which body organs are afflicted. Researchers have discovered a number of genes linked to an increased susceptibility of developing SLE. Type 11 is linked to a defect on chromosome 2q32.2-q32.3.
  • Systemic Lupus Erythematosus, Susceptibility to, 12: Systemic Lupus Erythematosus is an autoimmune disease affecting mostly women and causing various effects throughout different parts of the body. Its severity can range from very mild to extremely serious depending on which body organs are afflicted. Researchers have discovered a number of genes linked to an increased susceptibility of developing SLE. Type 12 is linked to a defect on chromosome 8p23.1.
  • Systemic Lupus Erythematosus, Susceptibility to, 13: Systemic Lupus Erythematosus is an autoimmune disease affecting mostly women and causing various effects throughout different parts of the body. Its severity can range from very mild to extremely serious depending on which body organs are afflicted. Researchers have discovered a number of genes linked to an increased susceptibility of developing SLE. Type 13 is linked to a defect on chromosome 6p23.
  • Systemic Lupus Erythematosus, Susceptibility to, 2: Systemic Lupus Erythematosus is an autoimmune disease affecting mostly women and causing various effects throughout different parts of the body. Its severity can range from very mild to extremely serious depending on which body organs are afflicted. Researchers have discovered a number of genes linked to an increased susceptibility of developing SLE. Type 2 is linked to a defect on chromosome 2q37.3.
  • Systemic Lupus Erythematosus, Susceptibility to, 3: Systemic Lupus Erythematosus is an autoimmune disease affecting mostly women and causing various effects throughout different parts of the body. Its severity can range from very mild to extremely serious depending on which body organs are afflicted. Researchers have discovered a number of genes linked to an increased susceptibility of developing SLE. Type 3 is linked to a defect on chromosome 4p16-p15.2.
  • Systemic Lupus Erythematosus, Susceptibility to, 4: Systemic Lupus Erythematosus is an autoimmune disease affecting mostly women and causing various effects throughout different parts of the body. Its severity can range from very mild to extremely serious depending on which body organs are afflicted. Researchers have discovered a number of genes linked to an increased susceptibility of developing SLE. Type 4 is linked to a defect on chromosome 12q24.
  • Systemic Lupus Erythematosus, Susceptibility to, 5: Systemic Lupus Erythematosus is an autoimmune disease affecting mostly women and causing various effects throughout different parts of the body. Its severity can range from very mild to extremely serious depending on which body organs are afflicted. Researchers have discovered a number of genes linked to an increased susceptibility of developing SLE. Type 5 is linked to a defect on chromosome 13q32.
  • Systemic Lupus Erythematosus, Susceptibility to, 6: Systemic Lupus Erythematosus is an autoimmune disease affecting mostly women and causing various effects throughout different parts of the body. Its severity can range from very mild to extremely serious depending on which body organs are afflicted. Researchers have discovered a number of genes linked to an increased susceptibility of developing SLE. Type 6 is linked to a defect on chromosome 16p11.2.
  • Systemic Lupus Erythematosus, Susceptibility to, 7: Systemic Lupus Erythematosus is an autoimmune disease affecting mostly women and causing various effects throughout different parts of the body. Its severity can range from very mild to extremely serious depending on which body organs are afflicted. Researchers have discovered a number of genes linked to an increased susceptibility of developing SLE. Type 7 is linked to a defect on chromosome 20p12.
  • Systemic Lupus Erythematosus, Susceptibility to, 8: Systemic Lupus Erythematosus is an autoimmune disease affecting mostly women and causing various effects throughout different parts of the body. Its severity can range from very mild to extremely serious depending on which body organs are afflicted. Researchers have discovered a number of genes linked to an increased susceptibility of developing SLE. Type 8 is linked to a defect on chromosome 20q13.1.
  • Systemic Lupus Erythematosus, Susceptibility to, 9: Systemic Lupus Erythematosus is an autoimmune disease affecting mostly women and causing various effects throughout different parts of the body. Its severity can range from very mild to extremely serious depending on which body organs are afflicted. Researchers have discovered a number of genes linked to an increased susceptibility of developing SLE. Type 9 is linked to a defect on chromosome 1q32.
  • Temporal arteritis: Inflamed head artery causing headache.
  • Varicose veins: Appearance of veins in the skin
  • Vein symptoms: Symptoms affecting the veins (blood vessels)
  • Wagener syndrome: A disorder involving the association of hypertension, arteriosclerosis, thickened heart muscle and severe neuroretinitis.
  • Wegener's granulomatosis: A rare disease involving blood vessel inflammation which can affect the blood flow to various tissues and organs and hence cause damage. The respiratory system and the kidneys are the main systems affected.
  • Werner syndrome: A form of premature aging where sufferers start aging during adolescence or soon after and appear old by the time they reach their 30's or 40's. Milder forms of the condition may also occur.
  • Xanthoma: Fatty deposits under the skin causing yellow bumps

Conditions listing medical symptoms: Artery symptoms:

The following list of conditions have 'Artery symptoms' or similar listed as a symptom in our database. This computer-generated list may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

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Conditions listing medical complications: Artery symptoms:

The following list of medical conditions have 'Artery symptoms' or similar listed as a medical complication in our database.

 

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