Assessment
Questionnaire

Have a symptom?
See what questions
a doctor would ask.
 
Symptoms » Nosebleeds » Glossary
 

Glossary for Nosebleeds

Medical terms related to Nosebleeds or mentioned in this section include:

  • ADP platelet receptor P2Y12, deficiency of: Deficiency of a compound (P2Y12) involved in the blood clotting process which results in bleeding problems.
  • Accelerated hypertension: Accelerated hypertension is a condition characterized by a rapid increase in blood pressure. The condition is a medical emergency which can cause organ damage if not treated promptly.
  • Accidental Eye Injury: The accidental injury to an eye
  • Acquired Aplastic Anemia: A rare disorder involving severe failure of the bone marrow to produce new blood cells. Acquired aplastic anemia means that the condition was not present at birth but developed during the persons lifetime. The condition may be caused by such things as autoimmune reactions, radiation and certain drugs, chemicals or viral infections.
  • Acquired prothrombin deficiency: A deficiency of prothrombin (vital for blood clotting) which is acquired through other conditions such as liver disease, anticoagulant drugs or vitamin K deficiency. The severity of symptoms is determined by the degree of deficiency.
  • Acute cholinergic dysautonomia: A rare condition characterized by the presence of abnormal red blood cells in the bone marrow and blood. The condition is characterized by anemia and generally leads to the development of acute myelogenous leukemia. The acute form has more severe symptoms than the chronic form.
  • Acute erythroleukemia: A rare condition characterized by the presence of abnormal blood cells (erythroblastic precursors) in the bone marrow and blood. The condition is characterized by anemia and generally leads to the development of acute myelogenous leukemia. The acute form has more severe symptoms than the chronic form.
  • Acute leukemia: An acute condition which affects a cell line of the blood which shows little or no differentiation
  • Acute lymphocytic leukemia: A malignant disease that starts suddenly and progresses quickly. It is characterized by a high number of immature cells in the organs, bone marrow and blood. Symptoms include fever, pallor, anorexia, fatigue, anemia, hemorrhage, bone pain, splenomegaly and frequent infections. Also called acute lymphoblastic leukemia.
  • Acute promyelocytic leukemia: A rare bone marrow cancer characterized by a lack of mature blood cells and excessive amounts of immature blood cells (promyelocytes).
  • Acute sinusitis: An acute inflammation of the sinuses
  • Adhesive abuse: Adhesive abuse is the use of various inhalants for the purpose of achieving a "high". They are often used as a cheap, readily available alternative to street drugs but they can cause serious damage to the body. Adhesives include household glues, rubber cement and model aeroplane glue. These adhesives can be abused by sniffing them, spraying directly into the mouth, heating them and then inhaling them or injecting them directly into the body.
  • Adhesive addiction: Adhesive addiction refers to the compulsive need to abuse adhesives (e.g. sniffing them). Sufferers have withdrawal symptoms when attempting to stop the habit and feel unable to stop the habit despite knowing the harm it is causing their health. Aerosols are very damaging to the body and can readily result permanent brain damage and even death. Death can occur through chronic use and in rare cases can occur after one session of use. Children and teenagers are particular at risk for this type of addiction - it is readily available and users feel it gains them greater acceptance from their peers. Adhesives includes household glue, rubber cement and model airplane glue.
  • Aerosol abuse: Aerosol abuse is the use of various inhalants for the purpose of achieving a "high". They are often used as a cheap, readily available alternative to street drugs but they can cause serious damage to the body. Aerosols include air fresheners, hair spray, spray pain and deodorants. These aerosols can be abused by sniffing them, spraying directly into the mouth, heating them and then inhaling them or injecting them directly into the body.
  • Aerosol addiction: Aerosol addiction refers to the compulsive need to abuse aerosol (e.g. sniffing them). Sufferers have withdrawal symptoms when attempting to stop the habit and feel unable to stop the habit despite knowing the harm it is causing their health. Aerosols are very damaging to the body and can readily result permanent brain damage and even death. Death can occur through chronic use and in rare cases can occur after one session of use. Children and teenagers are particular at risk for this type of addiction - it is readily available and users feel it gains them greater acceptance from their peers. Aerosols includes spray pain, air freshener, deodorants and hair sprays.
  • Aging: The medical conditions from getting older.
  • Allergies: Immune system over-reaction to various substances.
  • Antrochoanal polyp:
  • Aplastic anemia: A blood disorder where the bone marrow produces insufficient new blood cells.
  • Argentinean hemorrhagic fever: An infectious disease caused by the Junin virus. Transmission can occur through contact with infected rodent (usually the corn mouse) urine, feces or saliva. The incubation period lasts from one to two weeks. The disease is most common in rural workers in Argentina.
  • Asphyxiation: A condition which is characterized by the inability to respire
  • Aspirin -- Teratogenic Agent: There is strong evidence to indicate that exposure to Aspirin during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Autoimmune Lymphoproliferative Syndrome: An inherited autoimmune condition characterized by proliferation of lymphocytes and autoimmunity against the body's own blood cells resulting in premature death of certain blood cells.
  • Autoimmune Thrombocytopenia: Autoimmune disorder causing a lack of blood platelets.
  • Back tumour: The presence of tumour growth in the vertebra, whether due to primary malignancies e.g. leukaemic or myeloma infiltration of the bone marrow, or due to secondary metastases from another site e.g. lung or breast.
  • Banti Syndrome: A rare conditions where chronic congestive spleen enlargement causes it to destroy red blood cells too early. The spleen becomes enlarged due to an obstruction of blood flow in the organ and the resulting increase in blood pressure.
  • Banti's syndrome: A chronic, progressive condition marked by enlargement of the spleen which is associated with anemia, splenomegaly, ascites, jaundice, leucopenia, thrombocytopenia and gastrointestinal bleeding.
  • Barotrauma: Damage to the lungs, ear or sinuses caused by rapid or extreme changes in air pressure.
  • Benign mucosal pemphigoid: A rare chronic disease involving blistering and scarring of the mucous membranes especially in the mouth and conjunctiva of the eye.
  • Bernard-Soulier Syndrome: A congenital bleeding disorder marked by inability of platelets to coagulate or by insufficient platelets. The platelets that are present are often large.
  • Biliary cirrhosis: Biliary cirrhosis is a condition where the bile ducts are unable to transport bile effectively due to blockage, inflammation, scarring or some other damage to the bile ducts. The condition may result from such things as congenital defect of the bile ducts (e.g. biliary atresia), cystic fibrosis, gallstones or a variety of other secondary conditions. The cause of primary biliary cirrhosis is not fully understood.
  • Bing-Neel syndrome: A rare disorder involving infiltration of the central nervous system by abnormal leukemia-like cells (lymphoplasmocytoid cells) that occur in Waldenström's macroglobulinemia. The abnormality increases blood viscosity which impairs its circulation through small brain and eye blood vessels.
  • Bleeding disorders: Any disorder leading to bleeding or bruising.
  • Bleeding symptoms: Any type of bleeding symptoms.
  • Bolivian hemorrhagic fever: An infectious disease that occurs in Bolivia and is caused by the Machupo virus. Transmission can occur through contact with infected rodent (Calomys callosus) droppings. The incubation period lasts from one to two weeks.
  • Breath symptoms: Breath-related symptoms including breath odor
  • Breathing symptoms: Symptoms affecting the breathing systems.
  • Broken nose: Fracture of the nose
  • Brown snake poisoning: The Brown snake is a poisonous Australian snake. They are considered one of the most venomous snakes in the world and their bite can result in death without prompt medical attention. The snake venom contains toxins which affect the blood and nerve systems. Children tend to suffer more severe symptoms due to their smaller body size.
  • Chemical poisoning -- Anticoagulant rodenticide: Anticoagulant rodenticide is a chemical used to control rodents. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Biphenyl: Biphenyl is a chemical used mainly as a fungicide for fruit packaging and in textile dyes. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Borates: Borate is a chemical used in a wide variety of products - herbicides, paints, insecticides, rodenticides and various personal products such as skin creams, toothpastes and powders. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Brodifacoum: Brodifacoum is a chemical used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Bromadiolone: Bromadiolone is a chemical used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Calcium Sulfate: Calcium Sulfate is a chemical with a wide range of applications from soil conditioners and paint pigment to the manufacture of products such as plaster and tiles. It is also often used as a laboratory reagent. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Diquat Dibromide: Diquat Dibromide is a chemical used mainly in herbicides. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Formaldehyde: Formaldehyde is a chemical used mainly in blues, lacquers, fireproofing, electrical insulation, leather tanning products and embalming. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Metaldehyde: Metaldehyde is a chemical used mainly as a molluscicide, in heating fuel and in fire lighters. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Tetrachloroethylene: Tetrachloroethylene is a chemical used mainly as a fabric dry cleaner, degreaser, worming treatment for animals and in the manufacture of freons. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Tetryl: Tetryl is a chemical used mainly as a military explosive. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Vanadium: Vanadium is an element used mainly in steel alloys but is also used in glass coatings, electric fuel cells and other applications. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chlorophacinone rodenticide poisoning: Chlorophacinone is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Cholestasis, progressive familial intrahepatic 1: A rare inherited condition where bile is unable to drain from the liver where it builds up and causes progressive liver damage.
  • Christmas disease: Haemophilia B. An x-linked recessive form of haemophilia due to deficiency of coagulation factor IX
  • Chronic Sinusitis: Chronic inflammation of the sinuses
  • Chronic leukemia: Leukemia in which the cell line is well differentiated, usually B lymphocytes.
  • Chronic sinusitis: Chronic inflammation of the sinuses
  • Chronic vitamin A toxicity: Chronic excessive ingestion of vitamin A can cause symptoms.
  • Clotting disorders: Disorder with excessive clotting
  • Clotting symptoms: Symptoms affecting the blood's ability to clot
  • Coagulation disorders: Any disorder leading to bleeding or bruising.
  • Cocaine -- Teratogenic Agent: There is evidence to indicate that exposure to Cocaine during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Cocaine abuse: Stimulant drug with various effects
  • Cold-like symptoms: Symptoms similar to the common cold.
  • Common cold: Symptoms similar to the common cold.
  • Congenital Afibrinogenemia: A rare disorder involving the inability to make fibrinogen which is essential for the process of blood clotting.
  • Congenital aplastic anemia: A genetic disorder where the bone marrow does not produce enough blood cells. Fanconi's anemia is an example of congenital aplastic anemia.
  • Coumachlor rodenticide poisoning: Coumachlor is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Coumafuryl rodenticide poisoning: Coumafuryl is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Coumatetralyl rodenticide poisoning: Coumatetralyl is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Defibrination syndrome: The generation of fibrin in the blood and consumption of pro-coagulants and platelets occurring in complications of obstetrics
  • Deviated Septum: A septum in the nose that is deviated from the normal position
  • Difenacoum rodenticide poisoning: Difenacoum is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Difethialone rodenticide poisoning: Difethialone is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Diphacinone rodenticide poisoning: Diphacinone is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Dry nose: Dryness inside the nasal passages
  • Epistaxis: Bloody discharge from the nose.
  • Epstein's Syndrome: A syndrome characterized by the association of kidney disease, deafness and a blood disorder.
  • Essential thrombocytopenia: A rare blood disorder characterized by an excessively low number of platelets in the blood which often results in hemorrhages.
  • Essential thrombocytosis -- same as essential thrombocythemia: A rare blood disorder where the blood contains too many platelets due to excessive megakaryocytes (platelet-producing cells). Platelets are essential for blood clotting but in essential thrombocythemia excessive platelets can cause the blood to form abnormal clots. If the platelets are defective as well then bleeding problems can occur. The severity of the condition is variable.
  • Esthesioneuroblastoma: A rare type of tumor that occurs in the upper nasal cavity. The tumor may obstruct one or both nostrils.
  • Ethmoidal polyp:
  • Excessive dieting: Excessive limitation of food intake can lead to problems and effects such as dizziness, depression, intestinal problems, edema and impaired growth.
  • Face symptoms: Symptoms affecting the face
  • Factor V Quebec: An inherited bleeding disorder reported in Quebec, Canada.
  • Factor V deficiency: An inherited disorder where the deficiency of a blood component affects its ability to clot properly which can lead to bleeding problems. The severity of the disorder can vary from easy bruising to life-threatening hemorrhages.
  • Factor VII deficiency: A rare inherited blood disorder caused by a deficiency of a blood protein called Factor VII and resulting in poor blood coagulation. The severity of the condition is variable.
  • Factor X deficiency: A rare blood clotting disorder which may be inherited or acquired in people suffering from conditions such as liver disease, amyloidosis, leprosy and certain cancers. The underlying cause is the deficiency of a protein (Factor X) which is needed for the blood to clot properly. The condition may cause mild to severe bleeding depending on the degree of deficiency of Factor X.
  • Factor X deficiency -- Friuli: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Fruili variant tends to only cause moderate bleeding problems and occurs mainly in an area of Italy called Fruili.
  • Factor X deficiency -- Kanazawa: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Kanazawa variant results in reduced Factor X blood clotting activity.
  • Factor X deficiency -- Ketchikan: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Ketchikan variant results in reduced Factor X blood clotting activity.
  • Factor X deficiency -- Nottingham: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Nottingham variant results in reduced Factor X blood clotting activity.
  • Factor X deficiency -- Padua: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Padau variant results in reduced Factor X blood clotting activity.
  • Factor X deficiency -- San Antonio: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The San Antonia variant results in 14% of normal Factor X blood clotting activity.
  • Factor X deficiency -- Santo Domingo: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Santo Domingo variant results in reduced Factor X blood clotting activity.
  • Factor X deficiency -- Shanghai: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Shangai variant results in reduced Factor X blood clotting activity.
  • Factor X deficiency -- St. Louis II: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The St. Louis II variant results in reduced Factor X blood clotting activity.
  • Factor X deficiency -- Stockton: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Stockton variant results in reduced Factor X blood clotting activity.
  • Factor X deficiency -- Taunton: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Taunton variant results in reduced Factor X blood clotting activity.
  • Factor X deficiency -- Tokyo: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Tokyo variant results in reduced Factor X blood clotting activity.
  • Factor X deficiency -- Vorarlberg: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Vorarlberg variant results in reduced Factor X blood clotting activity.
  • Factor X deficiency -- Wenatchee I: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Wenatchee I variant results in reduced Factor X blood clotting activity.
  • Factor X deficiency -- Wenatchee II: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Wenatchee II variant results in reduced Factor X blood clotting activity.
  • Factor X deficiency -- autosomal dominant: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The autosomal dominant variant results in reduced Factor X blood clotting activity.
  • Familial platelet syndrome with predisposition to acute myelogenous leukemia: A rare inherited blood disorder that is associated with an increased risk of myeloid malignancies - especially acute myelogenous leukemia.
  • Fanconi's anemia: Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. An increased incidence of leukemias and other cancers is associated with this condition and various skeletal abnormalities and other birth defects may also be present. The condition is present at birth but symptoms of the blood problems are often not evident until later in childhood - in rare cases, the condition may not be diagnosed until adulthood.
  • Fanconi's anemia -- Complementation group A: Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group A refers to a genetic subtype of the disease. An increased incidence of leukemias and other cancers is associated with this condition and various skeletal abnormalities and other birth defects may also be present. The condition is present at birth but symptoms of the blood problems are often not evident until later in childhood - in rare cases, the condition may not be diagnosed until adulthood.
  • Fanconi's anemia -- Complementation group B: Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group B refers to a genetic subtype of the disease. An increased incidence of leukemias and other cancers is associated with this condition and various skeletal abnormalities and other birth defects may also be present. The condition is present at birth but symptoms of the blood problems are often not evident until later in childhood - in rare cases, the condition may not be diagnosed until adulthood.
  • Fanconi's anemia -- Complementation group C: Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group C refers to a genetic subtype of the disease. An increased incidence of leukemias and other cancers is associated with this condition and various skeletal abnormalities and other birth defects may also be present. The condition is present at birth but symptoms of the blood problems are often not evident until later in childhood - in rare cases, the condition may not be diagnosed until adulthood.
  • Fanconi's anemia -- Complementation group D1: Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group D1 refers to a genetic subtype of the disease. An increased incidence of leukemias and other cancers is associated with this condition and various skeletal abnormalities and other birth defects may also be present. The condition is present at birth but symptoms of the blood problems are often not evident until later in childhood - in rare cases, the condition may not be diagnosed until adulthood.
  • Fanconi's anemia -- Complementation group D2: Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group D2 refers to a genetic subtype of the disease. An increased incidence of leukemias and other cancers is associated with this condition and various skeletal abnormalities and other birth defects may also be present. The condition is present at birth but symptoms of the blood problems are often not evident until later in childhood - in rare cases, the condition may not be diagnosed until adulthood.
  • Fanconi's anemia -- Complementation group E: Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group E refers to a genetic subtype of the disease. An increased incidence of leukemias and other cancers is associated with this condition and various skeletal abnormalities and other birth defects may also be present. The condition is present at birth but symptoms of the blood problems are often not evident until later in childhood - in rare cases, the condition may not be diagnosed until adulthood.
  • Fanconi's anemia -- Complementation group F: Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group F refers to a genetic subtype of the disease. An increased incidence of leukemias and other cancers is associated with this condition and various skeletal abnormalities and other birth defects may also be present. The condition is present at birth but symptoms of the blood problems are often not evident until later in childhood - in rare cases, the condition may not be diagnosed until adulthood.
  • Fanconi's anemia -- Complementation group G: Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group G refers to a genetic subtype of the disease. An increased incidence of leukemias and other cancers is associated with this condition and various skeletal abnormalities and other birth defects may also be present. The condition is present at birth but symptoms of the blood problems are often not evident until later in childhood - in rare cases, the condition may not be diagnosed until adulthood.
  • Fanconi's anemia -- Complementation group I: Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group I refers to a genetic subtype of the disease. An increased incidence of leukemias and other cancers is associated with this condition and various skeletal abnormalities and other birth defects may also be present. The condition is present at birth but symptoms of the blood problems are often not evident until later in childhood - in rare cases, the condition may not be diagnosed until adulthood.
  • Fanconi's anemia -- Complementation group J: Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group J refers to a genetic subtype of the disease. An increased incidence of leukemias and other cancers is associated with this condition and various skeletal abnormalities and other birth defects may also be present. The condition is present at birth but symptoms of the blood problems are often not evident until later in childhood - in rare cases, the condition may not be diagnosed until adulthood.
  • Fanconi's anemia -- Complementation group L: Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group L refers to a genetic subtype of the disease. An increased incidence of leukemias and other cancers is associated with this condition and various skeletal abnormalities and other birth defects may also be present. The condition is present at birth but symptoms of the blood problems are often not evident until later in childhood - in rare cases, the condition may not be diagnosed until adulthood.
  • Fanconi's anemia -- Complementation group M: Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group M refers to a genetic subtype of the disease. An increased incidence of leukemias and other cancers is associated with this condition and various skeletal abnormalities and other birth defects may also be present. The condition is present at birth but symptoms of the blood problems are often not evident until later in childhood - in rare cases, the condition may not be diagnosed until adulthood.
  • Fanconi's anemia -- Complementation group N: Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group N refers to a genetic subtype of the disease. An increased incidence of leukemias and other cancers is associated with this condition and various skeletal abnormalities and other birth defects may also be present. The condition is present at birth but symptoms of the blood problems are often not evident until later in childhood - in rare cases, the condition may not be diagnosed until adulthood.
  • Fanconi's anemia -- Estren-Dameshek variant: Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The Estren-Dameshek variant is Fanconi's anemia without the presence of any physical malformations or deformities which are often associated with Fanconi's anemia. An increased incidence of leukemias and other cancers is associated with this condition. The condition is present at birth but symptoms of the blood problems are often not evident until later in childhood - in rare cases, the condition may not be diagnosed until adulthood.
  • Fibrinogen deficiency, congenital: A rare congenital disorder characterized by the inability to make fibrinogen which is essential for the process of blood clotting.
  • Fibrosing Mediastinitis idiopathic: A rare condition characterized by excessive growth of fibrous tissue and collagen deposits inside the chest which can compress various parts inside the chest such as the esophagus, airways and even some blood vessels.
  • Finale rodenticide poisoning: Finale is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Flocoumafen rodenticide poisoning: Flocoumafen is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Folgorat rodenticide poisoning: Folgorat is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Glomerulonephritis: A condition which affects the kidneys and is characterized by inflammatory changes that occur in the glomeruli
  • Glycogen Storage Disease Type I: An inherited metabolic disorder where a deficiency of the enzyme glucose-6-phosphatase prevents glycogen being turned into glucose leading to a buildup of glycogen in the liver and kidneys. Most problems tend to develop during adulthood.
  • Glycogen storage disease type 1C: A genetic metabolic disorder involving a deficiency of the enzyme glucose-6-phosphatase (due to a defect in the microsomal phosphate) which results in the accumulation of glycogen in various tissues. G6P is stored as glycogen until the body needs to convert it to a sugar for energy. The enzyme deficiency prevents the conversion and hence low blood sugar levels result.
  • Glycogen storage disease type 1D: A genetic metabolic disorder involving a deficiency of the enzyme glucose-6-phosphatase (due to a defect in the microsomal glucose transporter) which results in the accumulation of glycogen in various tissues. G6P is stored as glycogen until the body needs to convert it to a sugar for energy. The enzyme deficiency prevents the conversion and hence low blood sugar levels result.
  • Hantavirosis: Infection by hantavirus which is a virus from the family Bunyaviridae. Infection generally causes severe febrile illness which can involve bleeding, shock and even death in some cases. The disease is transmitted by infected rodents.
  • Havoc rodenticide poisoning: Havoc is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Head injury: Any injury that occurs to the head
  • Head symptoms: Symptoms affecting the head or brain
  • Hemoglobin S/hemoglobin Lepore, Boston: A blood disorder that mainly causes hemolytic anemia with great variability of symptoms.
  • Hemoglobin S/hemoglobin O, Arab: A genetic blood anomaly which causes severe hemolytic anemia, fever, pain, cramping and excessive bleeding.
  • Hemoglobin SC: A genetic blood disorder where the patient inherits a gene for hemoglobin S from one parent and hemoglobin C from another. Severity of symptoms is variable.
  • Hemophilia: Blood disease usually genetic causing failure to clot.
  • Hemorrhagic thrombocythemia: A rare blood disorder characterized by increased number of platelets in the blood which often results in an enlarged spleen, bleeding and blood vessel blockages.
  • Herbal Agent adverse reaction -- Clove: Clove can be used as a herbal agent that can be used topically for tooth pain or as a local anesthetic in dentistry. The herbal agent can cause an adverse reaction or even anaphylaxis in some people.
  • Herbal Agent adverse reaction -- Pennyroyal Oil: Pennyroyal Oil can be used as a herbal agent to treat delayed menstruation and as an insect repellent. The herbal agent can cause an adverse reaction in some people.
  • Hereditary hemorrhagic telangiectasia: A rare genetic disorder characterized by epistaxes and multiple telangiectases.
  • Hermansky-Pudlak Syndrome: A rare disorder characterized by various degrees of albinism, bleeding due to a platelet defect and accumulation of a waxy substance in cells (lysosomal ceroid storage).
  • Hermansky-Pudlak syndrome type 2: A rare disorder characterized by various degrees of albinism, bleeding due to a platelet defect, an accumulation of a waxy substance in cells (lysosomal ceroid storage) and immunodeficiency. HPS type 2 differs from type 1 in that it also involves immunodeficiency due to congenital neutropenia.
  • High Blood Pressure/Hypertension:
  • High blood pressure: Excessive blood pressure.
  • Hip cancer: The presence of tumour growth in the bone of the hip, whether due to primary malignancies e.g. leukaemic or myeloma infiltration of the bone marrow, or due to secondary metastases from another site e.g. lung or breast; cancer affecting bone of hip likely to affect other bones e.g. vertebra, ribs
  • Hypertension: Excessive blood pressure.
  • Hypertension due to bilateral renal artery stenosis: Hypertension due to bilateral renal artery stenosis is high blood pressure resulting from narrowing kidney blood vessels which prevents the blood from flowing through the kidneys properly.
  • Hypertension due to coarctation of the aorta: Hypertension due to coarctation of the aorta is high blood pressure resulting from a birth defect where a heart blood vessel called the aorta is abnormally narrowed. The high blood pressure tends to affect mainly the upper part of the body. Babies and very young children tend to have more severe symptoms as the degree of narrowing tends to be greater than in older children or adults.
  • Hypertension in children: Hypertension in children is a condition in which a child has an abnormal elevation in blood pressure.
  • Hypertension in children from 11 through adolescence: Hypertension in children from 11 through adolescence refers to a child between the ages of 11 years through adolescence who has an abnormal elevation in blood pressure.
  • Hypertension in children one to ten years: Hypertension in children one to ten years refers to a child between the ages of one to ten years who has an abnormal elevation in blood pressure.
  • Hypertension-like disorders:
  • Hypopigmented lesions in children: Hypopigmented lesions in children refers are sores or ulcers that are colorless or have lost color in a child.
  • Immune Thrombocytopenic Purpura: Reduced blood platelets causing visible skin blemishes from bleeding or bruising.
  • Immune thrombocytopenia: A rare disorder where the body's immune system attacks blood platelets which affect the blood's ability to clot.
  • Indandione rodenticide poisoning: Indandione is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Inhalant abuse: Inhalant abuse is the use of various inhalants for the purpose of achieving a "high". They are often used as a cheap, readily available alternative to street drugs but they can cause serious damage to the body. Inhalants include gasoline, adhesives, solvents, and aerosols. These inhalants can be abused by sniffing them, spraying directly into the mouth, heating them and then inhaling them or injecting them directly into the body.
  • Inhalant addiction: Inhalant addiction refers to the compulsive need to abuse inhalants (e.g. inhaling them). Sufferers have withdrawal symptoms when attempting to stop the habit and feel unable to stop the habit despite knowing the harm it is causing their health. Inhalants are very damaging to the body and can readily result permanent brain damage and even death. Death can occur through chronic use and in rare cases can occur after one session of use. Children and teenagers are particular at risk for this type of addiction - it is readily available and users feel it gains them greater acceptance from their peers. Inhalants includes glues, shoe polish, household cleaners, room deodorizers and nail polish removers.
  • Injury: Any damage inflicted in the body
  • Isotretinoin -- Teratogenic Agent: There is evidence to indicate that exposure to Isotretinoin (an acne treatment drug) during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Juvenile angiofibroma: A condition characterized by a benign tumour of the nasopharynx
  • Klerat rodenticide poisoning: Klerat is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Leprosy, susceptibility to, 1: A chronic, progressive infectious disease caused by Mycobacterium leprae which causes skin sores and also affects the eyes, mucous membranes and peripheral nerves. The range of manifestations and severity of symptoms is quite variable. Researchers have discovered a number of genetic mutations linked to an increased susceptibility to leprosy. Type 1 is linked to a defect on chromosome 10p13.
  • Leprosy, susceptibility to, 2: A chronic, progressive infectious disease caused by Mycobacterium leprae which causes skin sores and also affects the eyes, mucous membranes and peripheral nerves. The range of manifestations and severity of symptoms is quite variable. Researchers have discovered a number of genetic mutations linked to an increased susceptibility to leprosy. Type 2 is linked to a defect on chromosome 6q25.2-q27.
  • Leprosy, susceptibility to, 3: A chronic, progressive infectious disease caused by Mycobacterium leprae which causes skin sores and also affects the eyes, mucous membranes and peripheral nerves. The range of manifestations and severity of symptoms is quite variable. Researchers have discovered a number of genetic mutations linked to an increased susceptibility to leprosy. Type 3 is linked to a defect on chromosome 4q32 and 4p14.
  • Leprosy, susceptibility to, 4: A chronic, progressive infectious disease caused by Mycobacterium leprae which causes skin sores and also affects the eyes, mucous membranes and peripheral nerves. The range of manifestations and severity of symptoms is quite variable. Researchers have discovered a number of genetic mutations linked to an increased susceptibility to leprosy. Type 4 is linked to a defect on chromosome 6p21.3.
  • Leukemia: Cancer of the blood cells, usually white blood cells.
  • Leukocyte Adhesion Deficiency, Type III: A rare inherited disorder characterized by abnormal neutrophil functioning which reduces the body's immunity as well as bleeding problems due to platelet adhesive problems. The abnormal neutrophils are unable to be transported to sites of infection due to their inability to adhere to certain blood vessel components which would normally lead them to the infection site. Infections may be life-threatening as the body is unable to destroy bacteria effectively. Bleeding problems result from the inability of the blood platelets to clump together and stem the flow of blood.
  • Liver symptoms: Symptoms affecting the liver
  • Lymphomatoid Granulomatosis: A rare, progressive blood vessel disease where nodular lesions destroy blood vessels - lungs, skin and nervous system are mainly involved.
  • Machupo virus: A virus which is the cause of a form of hemorrhagic fever occurring in Bolivia
  • Malignant hypertension: Malignant hypertension is a condition characterized by very high blood pressure and swelling of the optic nerve. This type of hypertension is more common in people with kidney problems such as narrowed kidney blood vessels. The condition is a medical emergency which can cause organ damage if not treated promptly.
  • Matikus rodenticide poisoning: Matikus is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • May-Hegglin Anomaly: A rare inherited blood disorder involving abnormalities in some of the blood components (platelets and certain leukocytes). Some patients develop bleeding problems whereas other remain asymptomatic.
  • May-Hegglin thrombocytopenia: A rare inherited blood disorder involving abnormalities in some of the blood components (platelets and certain leukocytes). Some patients develop bleeding problems whereas other remain asymptomatic.
  • Menopause: End of female reproductive years
  • Mouser rodenticide poisoning: Mouser is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Mouth symptoms: Symptoms of the mouth or oral area.
  • Mucormycosis: An infectious disease caused by fungus from the order Mucorales which is normally found in the soil and in decaying plant matter. Transmission is usually through the inhalation of spores. It is generally harmless to healthy individuals but can cause infection in patients who are immunocompromised or who have a serious chronic illness such as uncontrolled diabetes. Symptoms and severity can vary considerable depending on the part of the body the infection occurs in - gastrointestinal tract, skin, lungs, central nervous system, eye orbit and the paranasal sinuses.
  • Myelodysplastic syndromes: A group of syndromes characterized by a disruption in the production of blood cells. Often the bone marrow increases production of various blood cells but because many of them are defective, they are destroyed before the reach the blood stream.
  • Myeloproliferative disease:
  • Nasal congestion: The congestion of the nasal passages.
  • Nasal polyp: A polyp that is found in the nasal passage
  • Nasal polyps: A growth or mass in the mucous membrane of the nasal passage
  • Nasopharyngeal carcinoma: A malignant cancer that occurs in the nasopharynx area which is the upper part of the throat. Often there are no symptoms until the cancer has metastasized to other parts of the body such as the neck.
  • Nasopharynx cancer: A condition which is characterized a malignancy located in the nasopharynx
  • Nose conditions: Any condition that affects the nose
  • Nose foreign body: Having a foreign body inserted in a nostril or otherwise in the nose.
  • Nose symptoms: Symptoms affecting the nose
  • Nosebleeds: Bleeding from the nose
  • Occupational Cancer -- Sino Nasal Carcinoma: Occupational exposure during soldering can increase the risk of developing sino nasal carcinoma.
  • Omsk hemorrhagic fever: A hemorrhagic fever caused by a virus. A serious outbreak occurred in Omsk and hence the name. Transmission occurs through tick bites. The infection has two phases: the first acute phase involves symptoms such as fever, rash and muscle pain and the second phase occurs after a week or two and involves the central nervous system (e.g. delirium, convulsions).
  • Osler-Rendu-Weber syndrome 2: A rare genetic disorder characterized by nosebleeds and multiple telangiectases that can occur on the skin, mucosal lining and internal organs. Type 2 tends to have a later onset than type 1 and there is a greater degree of liver involvement. It has a different genetic origin to type 1 and 3 (defect on chromosome 12q11-q14).
  • Osler-Rendu-Weber syndrome 3: A rare genetic disorder characterized by nosebleeds and multiple telangiectases that can occur on the skin, mucosal lining and internal organs. The occurrence of pulmonary arteriovenus fistulas in type 3 is greater than type 2 but less than in type 1. It has a different genetic origin to type 1 and 3 (defect on chromosome 5q31.3-q32).
  • Owren Parahemophilia: An inherited disorder where the deficiency of a blood component affects its ability to clot properly which can lead to bleeding problems. The severity of the disorder can vary from easy bruising to life-threatening hemorrhages.
  • PFIC: A rare inherited condition where bile is unable to drain from the liver where it builds up and causes progressive liver damage. End-stage liver disease usually occurs before adulthood. There are three different subtypes of the disorder, each with a different genetic origin of the defect.
  • Pancytopenia: A term used to describe a lack of all of the different types of blood cells - red and white blood cells and blood platelets. Cancer, infections and toxins are some of the causes of pancytopenia. Symptoms depend on the severity of the deficiency.
  • Pindborg Tumor: A rare type of slow growing, usually benign tumor that tends to develop in tissues associated with teeth. It is often associated with an impacted tooth. The tumor can be quite aggressive locally but rarely becomes malignant or metastasizes. The exact range and nature of the symptoms will vary depending on the location and size of the tumor.
  • Pindone rodenticide poisoning: Pindone is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Platelet disorder, familial, with associated myeloid malignancy: A blood disorder associated with the development of leukemia. The disorder arises from a genetic mutation.
  • Platelet function disorders: Any condition which affects the function of platelets
  • 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.
  • Polycythemia vera: Polycythemia vera refers to a condition in which there is an abnormal rise n the number of blood cells, especially red blood cells.
  • Prothrombin deficiency: A rare disorder involving a deficiency of a protein (prothrombin or factor II) involved in blood clotting. The severity of symptoms vary according to the level of deficiency.
  • Quebec platelet disorder: An inherited bleeding disorder reported in Quebec, Canada.
  • Ratak Plus rodenticide poisoning: Ratak Plus is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Relapsing fever: Tick-borne disease with symptoms that resolve and then relapse
  • Renal hypertension: Renovascular hypertension is high blood pressure resulting from narrowing or damage to kidney blood vessels which prevents the blood from flowing through the kidneys properly.
  • Renovascular Hypertension: Renovascular hypertension is high blood pressure resulting from narrowing or damage to kidney blood vessels which prevents the blood from flowing through the kidneys properly.
  • Resistant hypertension: Resistant hypertension is a form of high blood pressure that doesn't respond to treatment. Blood pressure remains high even when a combination of three drugs is used. It can be caused by such things a secondary hypertension, fluid retention or if the patient doesn't stick to the treatment plan.
  • Respiratory symptoms: Symptoms affecting the breathing systems.
  • Rhabdomyosarcoma of the orbit: A type of tumor found around the eye area (orbit). The tumor is usually malignant.
  • Rheumatic fever: An inflammatory disorder that can occur as a complication of untreated streptococcal bacterial infection such as strep throat or scarlet fever. The condition may affect the brain, skin, heart and joints.
  • Rhinocerebral mucormycosis: A rare opportunistic infection that tends to occur mainly in the brain and sinuses. The condition is usually fatal and generally only affects immunocompromised people such as patients with leukemia, lymphoma or those that have had organ transplants or chemotherapy. The infectious agent is saprophytic fungi.
  • Rhinocerebral zygomycosis: An infectious disease caused by fungus from the orders Mucorales and Entomophthorales which are normally found in the soil and in decaying plant matter. The infection differs from mucormycosis which only involves the order Mucorales. Transmission is usually through the inhalation of spores. It is generally harmless to healthy individuals but can cause infection in patients who are immunocompromised or who have a serious chronic illness such as uncontrolled diabetes. Symptoms and severity can vary considerable depending on the part of the body the infection occurs in - gastrointestinal tract, skin, lungs, central nervous system, eye orbit and the paranasal sinuses. Rhinocerebral zygomycosis involves infection of the paranasal sinuses and the central nervous system.
  • Rhinosporidiosis: An infectious disease caused by Rhinosporidium seeberi which occurs mainly in the nasal cavity or nearby mucosa-lined structures such as the conjunctiva. On rare occasions other parts of the body may be infected e.g. genital, rectum, ear and skin. The infection tends to persist for long periods of time (sometimes decades) and occasionally secondary bacterial infection can occur. Infection usually occurs through exposure to stagnant water contaminated with the infectious agent.
  • Rib symptoms: Symptoms affecting the ribs
  • Rodend rodenticide poisoning: Rodend is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Runny nose: Runny nasal discharge (medically named coryza)
  • Sarcoidosis: Rare autoimmune disease usually affecting the lungs.
  • Secondary Biliary Cirrhosis: Secondary biliary cirrhosis is a condition where the bile ducts are unable to transport bile effectively due to a secondary cause which results in blockage, inflammation, scarring or some other damage to the bile ducts. The condition may result from such things as congenital defect of the bile ducts (e.g. biliary atresia), cystic fibrosis, gallstones or a variety of other secondary conditions.
  • Secondary Hypertension: Secondary hypertension is high blood pressure resulting from an underlying cause such as kidney disease. Hypertension is a serious health condition due to the fact that it often causes no symptoms until it is severe.
  • Sickle Cell Anemia: Sickle cell anemia is an inherited blood disorder characterized by red blood cells which are crescent-shaped rather than the normal doughnut shape. These abnormally shaped red blood cells are unable to function normally and tend to undergo premature destruction which leads to anemia. If the genetic defect which causes the condition is inherited from both parents the condition can be quite severe whereas if it is inherited from only one parent, often there are no symptoms. The abnormally shaped red blood cells can cause problems when they clump together and block blood vessels.
  • Sinonasal undifferentiated carcinoma: A rare but aggressive tumor that occurs in the nasal or sinus cavities.
  • Sinus cancer: Cancer that originates from the mucosal tissue lining the sinus cavities or rarely from the bone itself.
  • Sinus symptoms: Symptoms affecting the sinuses
  • Sinusitis: Inflammation of the sinus passages (as a symptom)
  • Skull symptoms: Symptoms affecting the skull surrounding the brain.
  • Solvent abuse: Solvent abuse is the use of various inhalants for the purpose of achieving a "high". They are often used as a cheap, readily available alternative to street drugs but they can cause serious damage to the body. Solvents include nail polish removers, paint thinners, gasoline, typing correction fluid and toxic markers. These solvents can be abused by sniffing them, spraying directly into the mouth, heating them and then inhaling them or injecting them directly into the body.
  • Solvent addiction: Solvent addiction refers to the compulsive need to abuse solvents (e.g. sniffing them). Sufferers have withdrawal symptoms when attempting to stop the habit and feel unable to stop the habit despite knowing the harm it is causing their health. Solvents are very damaging to the body and can readily result permanent brain damage and even death. Death can occur through chronic use and in rare cases can occur after one session of use. Children and teenagers are particular at risk for this type of addiction - it is readily available and users feel it gains them greater acceptance from their peers. Solvents includes paint thinner, toxic markers, gasoline, cigarette lighter fluid, typing correction fluid and nail polish removers.
  • Stachybotrys chartarum: A toxic black slimy mold that can be found in damp indoor environments. Exposure can occur through the skin, ingestion or inhalation. It can causes conditions such as "sick building syndrome".
  • Stuart factor deficiency, acquired: A rare blood clotting disorder which causes mild to severe bleeding depending on the degree of deficiency of Factor X (Stuart factor). This disorder can be inherited or acquired by people suffering from conditions such as liver disease, amyloidosis, certain cancers and leprosy.
  • Stuart factor deficiency, congenital: A rare inherited blood clotting disorder which causes mild to severe bleeding depending on the degree of deficiency of Factor X (Stuart factor).
  • Superior vena cava syndrome: A condition caused by compression or obstruction to the normal circulation of the superior vena cava which carries deoxygenated blood from the body tissues back to the heart.
  • Systemic lupus erythematosus: chronic autoimmune disease that can be fatal, though with recent medical advances, fatalities are becoming increasingly rare.
  • Talon rodenticide poisoning: Talon is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Throat symptoms: Symptoms affecting the throat
  • Thrombasthenia: An inherited blood clotting disorder where abnormal blood platelet function causes results in excessive bleeding.
  • Thrombocytopathy: A blood disorder where abnormal blood platelets affect blood coagulation.
  • Thrombocytopenia: Decreased concentration of platelets in the blood.
  • Thrombocytopenic purpura, autoimmune: A rare blood disorder where a low number of platelets impairs the bloods ability to clot and results in bleeding into the skin and mucous membranes.
  • Timme syndrome: A syndrome involving insufficiency of the thymus, adrenal and pituitary glands. The disorder has involves three phases, each of which has varying symptoms: phase 1 is before puberty, phase 2 occurs after puberty and phase 3 tends to occur in the third decade.
  • Type I Glycogen Storage Disease: A condition which is characterized by a disease affecting glycogen storage
  • Typhoid fever: Fever from bacterial food poisoning.
  • Vitamin C deficiency: Indequate vitamin C in the diet
  • Volak rodenticide poisoning: Volak is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Volid rodenticide poisoning: Volid is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Von Gierke Disease: An inherited metabolic disorder where a deficiency of the enzyme glucose-6-phosphatase prevents glycogen being turned into glucose leading to a buildup of glycogen in the liver and kidneys.
  • Von Gierke disease IA: A genetic metabolic disorder involving a deficiency of the enzyme glucose-6-phosphatase which results in the accumulation of glycogen in various tissues. G6P is stored as glycogen until the body needs to convert it to a sugar and use it to create energy. The enzyme deficiency prevents the conversion and hence low blood sugar levels result.
  • Von Willebrand disease: A rare inherited blood coagulation disorder characterized by a deficiency or defect in plasma protein called the von Willebrand factor which leads to bleeding problems
  • Von Willebrand disease, platelet type: A condition that is characterised by autosomal inheritance and is a disorder that is charaterised by prolonged bleeding time.
  • Von Willebrand disease, type 1: A rare inherited blood coagulation disorder characterized by a deficiency in plasma protein called the von Willebrand factor which leads to bleeding problems. Most cases of von Willebrand disease are type 1 which is the mildest form of the condition. Patients rarely have severe bleeding problems but may bleed excessively during surgery, dental work or due to a traumatic injury.
  • Von Willebrand disease, type 2: A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 2 is further subdivided into 4 subtypes, each with a different underlying genetic defect. The different subtypes have different methods of treatment so an correct diagnosis is important. The severity of the bleeding symptoms is variable.
  • Von Willebrand disease, type 2A: A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 2 vWD is further subdivided into 4 subtypes, each with a different underlying genetic defect. The severity of the bleeding symptoms is variable.
  • Von Willebrand disease, type 2B: A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 2 vWD is further subdivided into 4 subtypes, each with a different underlying genetic defect. The severity of the bleeding symptoms is variable. Type 2B often requires a different medication to the other subtypes.
  • Von Willebrand disease, type 2M: A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 2 vWD is further subdivided into 4 subtypes, each with a different underlying genetic defect. Type 2M is very rare. The severity of the bleeding symptoms is variable.
  • Von Willebrand disease, type 2N: A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 2 vWD is further subdivided into 4 subtypes, each with a different underlying genetic defect. The severity of the bleeding symptoms is variable.
  • Von Willebrand disease, type 3: A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 3 is the most severe form of von Willebrand Disease.
  • Waldenstrom macroglobulinemia: A rare disorder involving malignancy of the lymph and blood cells.
  • 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.
  • Weil's syndrome: Severe form of Leptospirosis
  • Whooping Cough: An infectious condition caused by the bacteria Bordetella pertussis
  • X-linked dyserythropoietic anaemia and thrombocytopenia: An inherited blood disorder characterized by dyserythropeoietic anemia (abnormal red blood cell formation) and low blood platelet count which can cause bleeding problems.
  • Zygomycosis: An infectious disease caused by fungus from the orders Mucorales and Entomophthorales which are normally found in the soil and in decaying plant matter. The infection differs from mucormycosis which only involves the order Mucorales. Transmission is usually through the inhalation of spores. It is generally harmless to healthy individuals but can cause infection in patients who are immunocompromised or who have a serious chronic illness such as uncontrolled diabetes. Symptoms and severity can vary considerable depending on the part of the body the infection occurs in - gastrointestinal tract, skin, lungs, central nervous system, eye orbit and the paranasal sinuses.

Conditions listing medical symptoms: Nosebleeds:

The following list of conditions have 'Nosebleeds' 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.

Select from the following alphabetical view of conditions which include a symptom of Nosebleeds or choose View All.

View All A B C D E F G H I J K L M N O P Q R S T V W X Z

Conditions listing medical complications: Nosebleeds:

The following list of medical conditions have 'Nosebleeds' or similar listed as a medical complication in our database.
Last revision: Nov 21, 2003

 

By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.

Home | Symptoms | Diseases | Diagnosis | Videos | Tools | Forum | About Us | Terms of Use | Privacy Policy | Site Map | Advertise