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Symptom Checker » Elevated troponin » Dehydration
 

Elevated troponin and Dehydration
Symptom Checker

Results: Causes of Elevated troponin AND Dehydration

Note: Do not use for diagnosis; see limitations of results.

Results: 271 causes of Elevated troponin OR Dehydration

    1. Acidemia, methylmalonic
     An inborn error of metabolism where amino acids in the body aren't metabolized properly resulting in high levels of the acid throughout the body....more »
    2. Acidemia, propionic
     An inherited genetic disorder where the body is incapable of processing some proteins and fats resulting in the accumulation of certain substances in the body which causes the symptoms of the condition. The condition can be life threatening....more »
    3. Ackee Fruit Food poisoning
     Unripe ackee fruit contains a chemical called hypoglycin A and B which affect the central nervous system and fatty acid oxidation. Eating the unripe fruit can cause symptoms can occur in as little as two hours but is generally 6 to 48 hours. The ackee fru...more »
    4. Acute Pancreatitis
     Sudden severe inflammation of the pancreas causing digestive complaints....more »
    5. Addison's Disease
     A rare progressive hormonal disorder characterized by insufficient production of certain hormones called adrenal corticosteroids....more »
    6. Addisonian crisis
     Severe adrenal gland complication from Addison's disease....more »
    7. Adrenal Cortex Diseases
     Diseases of the adrenal cortex. Examples includes Addison's disease, Cushing's syndrome and adrenal fatigue....more »
    8. Adrenal crisis
     A condition which is characterized by insufficient amounts of the adrenocortical hormones that results in vomiting, nausea, hypotension and electrolyte abnormalities...more »
    9. Adrenal gland hypofunction
     Reduced adrenal gland activity due to damage to the adrenal gland or lack of stimulation of the gland. Pituitary hormones stimulate adrenal gland activity....more »
    10. Adrenal hyperplasia
     A group of disorder that occur when there is a problem in the process of making adrenal corticosteroids....more »
    11. Adrenal hyperplasia, congenital type 3
     A group of disorders that occur when a deficiency of 21-hydroxylase impairs the normal process of making adrenal corticosteroids. The severity of the condition is variable depending on the degree of deficiency....more »
    12. Adrenal hypofunction
     A condition which is characterized by a lack of production of hormones from the adrenal gland....more »
    13. Adrenal hypoplasia congenital, X-linked
     A genetic disorder which affects the body tissues that produce hormones. It is characterized by underdeveloped adrenal glands which results adrenal insufficiency and hypogonadotrophic hypogonadism....more »
    14. Alcohol abuse
     Excessive use of alcohol ranging from binge drinking to severe alcoholism...more »
    15. Amebiasis
     An intestinal infection caused by a parasitic amebic organism. It is usually associated with poor sanitation....more »
    16. Aminophyllin -- Teratogenic Agent
     Experimental studies on rats indicate that the use of Aminophyllin during pregnancy may cause various harmful effects on the fetus. The likelihood and severity of symptoms may be affected by the level of exposure and the stage of pregnancy that the exposu...more »
    17. Amyloid cardiopathy
     Amyloidosis is a rare group of metabolic disorders where a protein called amyloid accumulates in body organs and tissues where it can cause damage and is potentially fatal. The cardiac form involves deposits of amyloid in the heart muscle which affects it...more »
    18. Anemic -- hematuria syndrome
     An epidemic disease in Argentina which has a prolonged recovery time but usually there are no complications. Symptoms vary between seasons so that affected patients suffer anorexia, vomiting, diarrhea and dehydration in summer but suffer reduced urination...more »
    19. Angelman-Like Syndrome, X-linked
     A very rare syndrome characterized mainly by mental retardation, mutism, facial anomalies, epilepsy and weak eye muscles. Males tended to have severe mental retardation whereas female carriers had mild or no mental retardation. Patients do eventually walk...more »
    20. Angina
     A special type of chest pain....more »
    21. Anorexia Nervosa
     A disorder where a distorted sense of body image leads to self-starvation to the point of death in some cases....more »
    22. 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...more »
    23. Astrovirus
     An RNA virus that may affect the gastrointestinal system...more »
    24. Autoimmune enteropathy
     A very rare condition that occurs when the body's own immune system attacks the intestinal wall and affect the way it absorbs food....more »
    25. Autoimmune enteropathy, type 1
     A rare condition involving autoimmune problems which can variably manifest as enteropathy (diarrhea), hemolytic anemia, and endocrine gland diseases such as diabetes mellitus and thyroid disease. Resistance to viral infections is poor. The condition is li...more »
    26. Azalea poisoning
     Bacillus cereus is a bacterium that can cause food poisoning symptoms such as vomiting and diarrhea. There are two types: Type I causes mainly vomiting and is associated with fried rice whereas type II causes mainly diarrhea and is associated with meats, ...more »
    27. Bacillus cereus type I food poisoning
     Bacillus cereus is a bacterium that can cause food poisoning symptoms such as vomiting and diarrhea. There are two types: Type I causes mainly vomiting and is associated with fried rice whereas type II causes mainly diarrhea and is associated with meats, ...more »
    28. Bacillus cereus type II food poisoning
     Bacillus cereus is a bacterium that can cause food poisoning symptoms such as vomiting and diarrhea. There are two types: Type I causes mainly vomiting and is associated with fried rice whereas type II causes mainly diarrhea and is associated with meats, ...more »
    29. Balantidiasis
     Intestinal infection with a parasitic protozoa (Balantidium coli) resulting in intestinal inflammation. It is usually transmitted through direct or indirect contact with pig fecal matter....more »
    30. Bell mania
     A rare life-threatening neuropsychiatric disorder involving delusions, hyperactivity and periods of fever. Death can occur within days or months without treatment....more »
    31. Beta ketothiolase deficiency
     A rare inherited disease characterized by the bodies inability to metabolise certain amino acids and products of the breakdown of fat. Harmful levels of organic acids build up in the body and cause ketoacidic attacks....more »
    32. 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....more »
    33. Bowel Obstruction
     Blockage in the bowel of the digestive tract....more »
    34. Brainerd diarrhea
     Diarrheal condition of unknown cause....more »
    35. Burns
     Injury from burns and scalds....more »
    36. Bébé Collodion syndrome
     A rare birth abnormality where an infant is born covered in a tight, yellow, shiny membrane. The membrane peels off and may reform several times. As the membrane dries it can leave crack which can result in infection, dehydration or inability to control b...more »
    37. Calcitriol -- Teratogenic Agent
     There is strong evidence to indicate that exposure to Calcitriol 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 e...more »
    38. Campylobacter food poisoning
     Common bacterial infection usually from chicken....more »
    39. Carcinoid syndrome
     Carcinoid heart disease is a rare, metastatic disease that occurs predominantly in the right heart. The tricuspid and pulmonic valves are affected, leading to right heart failure, which results in increased morbidity and mortality....more »
    40. 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. ...more »
    41. Chicken soup poisoning
     The consumption of excessive amounts of chicken soup can result in serious symptoms due to very high salt levels in the body. Children and the elderly are more likely to be affected by the high salt levels of chicken soup however the condition is rarely s...more »
    42. Cholera
     An acute bacterial disease transmitted through food or water contaminated with human faeces. The intestinal infection is caused by the bacterium Vibrio cholerae....more »
    43. Chromosome 10, Monosomy 10p
    44. Chromosome 10p deletion syndrome
     A rare chromosomal disorder where there is a deletion of the short arm (p) of chromosome 10 resulting in variable abnormalities....more »
    45. Chromosome 9, Tetrasomy 9p
     A rare chromosomal disorder where there is four copies of the short arm of chromosome 9 instead of the normal two resulting in various abnormalities....more »
    46. Chromosome 9, trisomy 9p
     A rare chromosomal disorder where a portion of the short arm (p) of chromosome 9 is duplicated so there is three copies of it instead of the normal two....more »
    47. Chromosome 9p tetrasomy syndrome
     A rare chromosomal disorder where there is four copies of the short arm of chromosome 9 instead of the normal two resulting in various abnormalities....more »
    48. Chronic kidney failure
     Gradual failure of the kidneys over a period of time...more »
    49. Clostridium perfringens food poisoning
     Common type of food poisoning....more »
    50. Cocaine overdose
     Cocaine is an illegal and highly addictive recreational drug. Excessive doses of the drug can result in various symptoms and even death in severe cases....more »
    51. Cockayne syndrome
     A rare genetic disorder characterized by a senile-like appearance, hearing and vision impairment and sun sensitive skin....more »
    52. Cockayne syndrome type 1
     A rare inherited condition characterized by short stature, light sensitivity and a prematurely aged appearance. Type 1 is an early-onset form and involves progressive symptoms that usually start after 1 year of age....more »
    53. Cockayne syndrome type 2
     A rare inherited condition characterized by severely impaired neurological development. Type 2 is a congenital form of the disorder and symptoms are apparent from birth....more »
    54. Codeine withdrawal
     Symptoms that occur when Codeine use is discontinued or reduced. Codeine is a sedative pain-killer. Symptoms may vary depending on the level of dependence....more »
    55. Colchicine toxicity
     The toxic reaction of the body to the substance, possibly via allergic reaction or overdose....more »
    56. Colibacillosis
     Infection with a bacteria called Escherichia coli. Infection can cause severe diarrhea or septicemia. The bacteria can also produce toxins which can affect other parts of the body also. Infections can occur anywhere in the world but some developing countr...more »
    57. Colonic volvulus
     Twisting of the colon....more »
    58. Congenital Malabsorptive Diarrhea, 4
     A congenital condition characterized by diarrhea and malabsorption resulting form a reduced number of enteroendocrine cells. Enteroendocrine cells are found mainly in the pancreas but also in the gastrointestinal tract and they produce various hormones ne...more »
    59. Congenital adrenal hyperplasia (CAH)
     A group of disorder that occur when there is a problem in the process of making adrenal corticosteroids....more »
    60. Congenital adrenal hyperplasia -- sodium-wasting form
     A group of disorder that occur when a deficiency of 21-hydroxylase impairs the normal process of making adrenal corticosteroids - a severe deficiency of 21-hydroxylase causing salt-wasting which is potentially fatal....more »
    61. Congenital chloride diarrhea
     A rare birth disorder where the intestines don't absorb electrolytes properly (especially chloride) which leads to electrolyte imbalance which is potentially fatal if untreated. Symptoms often start while the infant is still inside the womb....more »
    62. Congenital lactase deficiency
     A congenital metabolic disorder where a deficiency of an enzyme called lactase impairs the body's ability to digest milk and other products that contain lactose. Symptoms tend to occur soon after consuming such products. The severity of symptoms depends o...more »
    63. Congenital sucrose-isomaltose malabsorption
     A rare disorder where a congenital deficiency of an enzyme (sucrase-isomaltase) prevents the absorption of sucrase and isomaltose consumed in the diet....more »
    64. Corticosterone Methyloxidase type I Deficiency
     A very rare genetic disorder where deficiency of a particularly chemical (aldosterone synthase) results in a deficiency of aldosterone. The condition can be severe enough to cause infant death unless the patient is diagnosed and treated....more »
    65. Crohn's disease
     Crohn's disease causes inflammation of the digestive system. It is one of a group of diseases called inflammatory bowel disease. The disease can affect any area from the mouth to the anus. It often affects the lower part of the small intestine called the ...more »
    66. Croup
     Respiratory infection with a characteristic cough...more »
    67. Cryptosporiosis
     Contagious parasitic digestive infection...more »
    68. Cutaneous photosensitivity colitis, lethal
     A very rare syndrome where extreme sun sensitivity of the skin is associated with difficult to treat diarrhea. Death often occurs during infancy....more »
    69. Cyclic vomiting syndrome
     A rare disorder involving repeated cyclic episodes of vomiting which occur for no obvious reason....more »
    70. Cystic fibrosis -- gastritis -- megaloblastic anemia
     A very rare syndrome characterized primarily by cystic fibrosis, anemia and gastritis....more »
    71. Cystinosis
     A rare biochemical disorder involving the accumulation of a chemical called cystine in various parts of the body which can cause harmful effects....more »
    72. Decreased chloride
    73. Defect in synthesis of adenosylcobalamin
     A rare genetic disorder characterized by the impaired ability to make a chemical called adenosylcobalamin. Adenosylcobalamin is a derivative of vitamin B12. The defect results a biochemical abnormality which affects the body's normal biochemical functioni...more »
    74. Dehydration
     Loss of fluids in the body...more »
    75. Developmental Lactase Deficiency
     This form of lactase deficiency occurs in premature infants. Lactase enzyme activity usually develops late in pregnancy so a preterm infant will not yet have developed this enzyme function. The greater the degree of prematurity, the greater the reduction ...more »
    76. Diabetes Insipidus
     Rare pituitary disorder often affecting the kidneys....more »
    77. Diabetes Insipidus, Neurogenic
     A disturbed water balance due to a deficiency of vasopressin (antidiuretic) hormone which causes excessive thirst and urination. Causes include autoimmune disease, malignancy, trauma, infection and blood vessel disease....more »
    78. Diabetes insipidus, diabetes mellitus, optic atrophy
     A rare association of diabetes insipidus, diabetes mellitus, optic atrophy, and deafness....more »
    79. Diabetes insipidus, nephrogenic type 2
     A rare congenital condition where the kidney fails to respond to the antidiuretic hormone (arginine vasopressin), thus preventing reabsorption of water. This results in excessive urination and thirst. Type II is specifically caused by a defect in the AQP2...more »
    80. Diabetes insipidus, nephrogenic, dominant type
     A rare dominantly inherited, congenital condition where the kidney fails to respond to the antidiuretic hormone (arginine vasopressin), thus preventing reabsorption of water. This results in excessive urination and thirst. The condition is specifically ca...more »
    81. Diabetes insipidus, nephrogenic, recessive type
     A rare recessively inherited, congenital condition where the kidney fails to respond to the antidiuretic hormone (arginine vasopressin), thus preventing reabsorption of water. This results in excessive urination and thirst. The condition is specifically c...more »
    82. Diabetes mellitus, congenital insulin-dependent, with fatal secretory diarrhea
     A rare condition involving autoimmune problems which can variably manifest as enteropathy (diarrhea), hemolytic anemia, and endocrine gland diseases such as diabetes mellitus and thyroid disease. Resistance to viral infections is poor. The condition is li...more »
    83. Diabetes mellitus, transient neonatal
     A form of infant diabetes that starts usually in the month of life but then usually disappears within a year. The condition predisposes the infant to diabetes later in life....more »
    84. Diabetic Ketoacidosis
     Life-threatening complication of high blood sugars and diabetes....more »
    85. Diarrhea
     Loose or watery stool....more »
    86. Diarrhea -- polyendocrinopathy -- infections, X-linked
     A rare X-linked disorder characterized by diarrhea and severe, fatal infections during infancy. The body's immune system attacks it's own endocrine glands and various other organs. Females are carriers and can have mild symptoms whereas males suffer the f...more »
    87. Diarrhea 2, with Microvillous Atrophy
     A rare congenital condition characterized by diarrhea resulting form a defect in small intestine....more »
    88. Diarrhea, polyendocrinopathy, fatal infection syndrome, X-linked
     A rare condition involving autoimmune problems which can variably manifest as enteropathy (diarrhea), hemolytic anemia, and endocrine gland diseases such as diabetes mellitus and thyroid disease. Resistance to viral infections is poor. The condition is li...more »
    89. Dilor -- Teratogenic Agent
     There is evidence to indicate that exposure to Dilor (a bronchodilator) 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 lev...more »
    90. Disulfiram toxicity
     The toxic reaction of the body to the substance, possibly via allergic reaction or overdose....more »
    91. Duodenal atresia
     A rare birth defect where a portion of the small intestine is absent or completely closed off and the digestive products cannot pass through. It is usually associated with other birth defects....more »
    92. Duodenal atresia tetralogy of Fallot
     A rare birth defect characterized by a heart defect and an intestinal malformation where the duodenum is absent or closed off which prevents digested material passing through....more »
    93. Dyphylline -- Teratogenic Agent
     There is evidence to indicate that exposure to Dyphylline (a bronchodilator) 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 th...more »
    94. E-coli food poisoning
     Type of bacterial food poisoning...more »
    95. Ecstasy abuse
     Use of the illicit drug called ecstasy...more »
    96. Endocrine-Cerebroosteodysplasia
     A rare condition observed in six members from two families. The condition is severe with all affected individuals dying before, during or soon after birth. A number of the pregnancies were voluntarily terminated due to the detected malformations. Endocrin...more »
    97. Enteric Anendocrinosis
     A congenital condition characterized by diarrhea and malabsorption resulting form a reduced number of enteroendocrine cells. Enteroendocrine cells are found mainly in the pancreas but also in the gastrointestinal tract and they produce various hormones ne...more »
    98. Enteroaggregative E. Coli infection
     A bacterial infection that results from ingesting contaminated food or water and results in diarrhea that tends to last for weeks. It most often causes diarrhea in children in developing countries. Enteroaggregative refers to the grouping nature of the ba...more »
    99. Enterohemorrhagic E. Coli infection
     A bacterial infection that results from ingesting contaminated food or water and results in bloody diarrhea. Enterohemorrhagic refers to the intestinal bleeding associated with the infection....more »
    100. Enteroinvasive E. Coli infection
     A type of bacterial infection that results from ingesting contaminated food or water and results in gastroenteritis. Enteroinvasive refers to the invasion of bacteria into the gastrointestinal lining. It tends to occur as occasional outbreaks in developed...more »
    101. Enteropathogenic E. Coli infection
     A bacterial infection that results from ingesting contaminated food or water and results in watery and sometimes bloody diarrhea. It most often causes diarrhea in infants in developing countries. Contaminated drinking water and meat products are the main ...more »
    102. Enteropathy, autoimmune, with hemolytic anemia and polyendocrinopathy
     A rare condition involving autoimmune problems which can variably manifest as enteropathy (diarrhea), hemolytic anemia, and endocrine gland diseases such as diabetes mellitus and thyroid disease. Resistance to viral infections is poor. The condition is li...more »
    103. Enterotoxigenic E. Coli infection
     A bacterial infection that results from ingesting contaminated food or water and results in diarrhea. It most often causes diarrhea in infants and travelers in underdeveloped countries where there is poor sanitation. Contaminated drinking water, soft chee...more »
    104. Epidermalolysis bullosa
     A group of skin disorders characterized by fragile skin which can blister upon little or no trauma to the skin. There are a number of different subtypes with some being inherited and some acquired. The hands and feet are often the main parts of the body a...more »
    105. Epidermolysis bullosa, junctional
     A rare inherited skin disease which is characterized by fragile skin which readily forms skin blisters and can result in fatal complications....more »
    106. Epidermolysis bullosa, lethal acantholytic
     A very rare inherited disorder characterized by extremely fragile skin and mucous membranes which blisters and peels. The majority of the skin blisters and peels within a week of birth. Severe fluid loss and death follows soon after....more »
    107. Epidermolysis bullosa, simplex
     A group of skin disorders characterized by fragile skin which can blister upon little or no trauma to the skin. There are a number of different subtypes with some being inherited and some acquired. The hands and feet are often the main parts of the body a...more »
    108. Epidermolytic epidermolysis bullosa
     A group of skin disorders characterized by fragile skin which can blister upon little or no trauma to the skin. There are a number of different subtypes with some being inherited and some acquired. The hands and feet are often the main parts of the body a...more »
    109. Epiglotitis
     Inflamation of the epiglottis in the throat...more »
    110. Epiglottiditis
     A condition characterized by inflammation of the epiglottis of the throat...more »
    111. Erythroderma
     Condition with thickening and flaking skin...more »
    112. Erythrodermic eczema
     Erythrodermic eczema is a severe condition that results from worsening eczema....more »
    113. Excessive dieting
     Excessive limitation of food intake can lead to problems and effects such as dizziness, depression, intestinal problems, edema and impaired growth....more »
    114. Exudative retinopathy familial, X-linked, recessive
     A rare progressive eye disorder which is inherited in a recessive X-linked manner. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function. The disorder is ca...more »
    115. Exudative retinopathy familial, autosomal dominant
     A rare progressive eye disorder which is inherited in a dominant manner. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function. The disorder is caused by a ...more »
    116. Exudative retinopathy familial, autosomal recessive
     A rare progressive eye disorder which is inherited in a recessive manner. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function....more »
    117. Exudative retinopathy, familial
     A rare progressive eye disorder which is inherited in a familial manner. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function....more »
    118. Exudative vitreoretinopathy 3
     A rare progressive eye disorder caused by a genetic defect on chromosome 11p13-p12. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function....more »
    119. Exudative vitreoretinopathy 4
     A rare progressive eye disorder caused by a genetic defect on chromosome 11q13.4. It can be inherited in a dominant or recessive manner. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels wh...more »
    120. Familial Lactase Deficiency
     A congenital metabolic disorder where normal amounts of lactase are produced but the lactase is defective and unable to digest milk and other products that contain lactose. Symptoms tend to occur soon after consuming such products....more »
    121. Fanconi's syndrome
    122. Fanconi-ichthyosis-dysmorphism
     A very rare syndrome characterized by scaly skin (ichthyosis), anemia, muscle anomalies and various other abnormalities. All six reported cases died within 6 months....more »
    123. Fever
     Elevation of the body temperature above the normal 37 degrees celsius...more »
    124. Food poisoning
     Poisoning from a substance or microbe in food....more »
    125. Fungal meningitis
     Fungal meningitis is an infection that causes swelling and irritation of the tissue around the brain and spinal cord. It usually strikes people whose weakened immune systems can't fight off infection. The disease is not common. but it can be very serious....more »
    126. Galactosemia I
     A rare inherited disorder where deficiency of a particular enzyme (galactose-1-phosphate uridyl transferase) prevents the metabolism of galactose which is a sugar component of milk. Ranges from milk intolerance in mild cases to death in severe untreated c...more »
    127. Gastritis
     Inflammation of the stomach lining...more »
    128. Gastroenteritis
     Acute stomach or intestine inflammation...more »
    129. Gastrointestinal bleeding
     Internal bleeding in the digestive tract...more »
    130. Gastrointestinal infections related to AIDS
     It usually occurs due to decreased immunity....more »
    131. Generalized pustular psoriasis
     This is a rare form of psoriasis is also known as von Zumbusch psoriasis. It can be life-threatening especially in the elderly. It is characterized by the development of pustules in the flexural areas - the backs of the knees, the insides of the elbows, t...more »
    132. Gingivostomatitis
     Mouth infection typically from first exposure to cold sores and subsequent viral HSV-1 infection....more »
    133. Glucose-galactose malabsorption
     An inherited metabolic disorder where the small intestine is unable to absorb and transport glucose and galactose that is consumed in the diet due to a lack of intestinal monosaccharidase....more »
    134. Green gill mushroom poisoning
     Green gill is a type of mushroom with a smooth cap and white gills eventually turning greenish. The mushroom is commonly found growing naturally in the US. This mushroom is very poisonous and causes severe gastrointestinal symptoms. Severe poisoning can l...more »
    135. HIV-1, CRF36_cpx
     HIV is an immune system disease caused by the HIV virus. AIDS is a term used when a person infected with HIV has a CD4+ T cell count below 200 or 14% of lymphocytes. AIDS is an advanced form of HIV. To be classified as AIDS the person must also have an AI...more »
    136. HMG-CoA lyase deficiency
     A rare inherited metabolic disorder where deficiency of a particular enzyme impairs the processing of amino acids in food to create energy and causes various symptoms. Stresses on the body such as infection, fasting and heavy exercise can trigger an episo...more »
    137. HOTS
     High blood calcium levels and bone resorption that occurs in some patients with T-cell lymphoma which is a cancer of the white blood cells....more »
    138. Hand-Foot-Mouth Syndrome
     An infectious viral disease caused by the coxsackievirus A. The disease is characterized by the development of blisters in the mouth and on hands and feet. The disease is spread by contact with body fluids from an infected person and the incubation period...more »
    139. Heart attack
     Serious and often fatal acute heart condition...more »
    140. Heat cramps
     Muscle cramps related to exertion...more »
    141. Heat exhaustion
     Overheating of the body with exhaustion or collapse...more »
    142. Heatstroke
     Heat exhaustion and collapse from heat exposure...more »
    143. Helminthiasis
     Infection of the human body with a parasitic worm such as roundworms and pinworms. The worms usually only involve the intestinal tract but sometimes they may invade other organs. The type and severity of symptoms is determined by the type of worm and the ...more »
    144. Hereditary primary Fanconi disease
     A rare inherited disorder characterized by defective reabsorption of various substances such as phosphate, potassium, amino acids and glucose which manifests as a wide range of abnormalities and problems....more »
    145. Herpes stomatitis
     Mouth infection with ulcers/blisters due to the herpes virus...more »
    146. Hyperemesis Gravidarum
     Rare condition of excessive vomiting during pregnancy...more »
    147. Hyperglycemia
     High levels of glucose in the blood...more »
    148. Hyperglycemic Hyperosmolar Nonketotic Syndrome
     Life-threatening complication of high blood sugars and diabetes....more »
    149. Hyperosmolar hyperglycemic nonketotic syndrome
     A form of diabetic coma seen in type 2 diabetes mellitus...more »
    150. Hyperparathyroidism
     Increased secretion of parathyroid hormone from the parathyroid glands....more »
    151. Hyperreninemic Hypoaldosteronism, Familial 2
     A very rare genetic disorder where deficiency of a particularly chemical results in a deficiency of aldosterone. The condition can be severe enough to cause infant death unless the patient is diagnosed and treated....more »
    152. Hyperthermia -- Teratogenic Agent
     There is strong evidence to indicate that hyperthermia 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 an...more »
    153. Hypoadrenalism
     Reduced adrenal gland activity....more »
    154. Hypoadrenocorticism -- hypoparathyroidism -- moniliasis
     An autoimmune disorder where hormone production by various glands is reduced. The main features of the disorder are Addison disease and/or hypoparathyroidism and/or chronic candidiasis....more »
    155. Hypoaldosteronism, familial
     A very rare genetic disorder where deficiency of a particularly chemical (aldosterone synthase) results in a deficiency of aldosterone. The condition can be severe enough to cause infant death unless the patient is diagnosed and treated....more »
    156. IPEX syndrome
     A rare condition involving autoimmune problems which can variably manifest as enteropathy (diarrhea), hemolytic anemia, and endocrine gland diseases such as diabetes mellitus and thyroid disease. Resistance to viral infections is poor. The condition is li...more »
    157. Ichthyosis congenita, Harlequin fetus type
     A very rare genetic skin disorder where a newborn is covered with large plates of thick skin that cracks and splits....more »
    158. Ichthyosis congenita, harlequin type
     A very rare genetic skin disorder where a newborn is covered with large plates of thick skin that cracks and splits....more »
    159. Immune dysregulation -- polyendocrinopathy -- enteropathy, X linked
     A rare condition involving autoimmune problems which can variably manifest as enteropathy (diarrhea), hemolytic anemia, and endocrine gland diseases such as diabetes mellitus and thyroid disease. Resistance to viral infections is poor. The condition is li...more »
    160. Intermediate cystinosis
     Cystinosis is a condition where excess amino acid cystine builds up to harmful levels in the body. The intermediate form of cystinosis starts later than the nephropathic form but the symptoms are the same....more »
    161. Intestinal epithelial dysplasia
     A rare intestinal disorder characterized by defects in the intestinal lining which results in severe chronic diarrhea usually soon after birth. Parenteral nutrition is usually required long term which can result in various complications and thus an intest...more »
    162. Intractable diarrhea of infancy (generic term)
     A group of disorder characterized by severe, difficult to treat, chronic diarrhea that starts during infancy. There a number of different disorders that can cause this condition - autoimmune enteropathy, congenital villous atrophy and syndromic diarrhea. ...more »
    163. Intractable diarrhea with enterocytes assembly abnormalities, congenital, familial
     An inherited disorder characterized by severe, chronic diarrhea in infants due to defects in the intestinal absorptive cells called enterocytes....more »
    164. Janbon syndrome
     Gastrointestinal symptoms that can occur when using a drug called oxytetracycline which is a type of antibiotic. The drug tends to destroy the good bacteria in the gastrointestinal system and allows other bacteria resistant to the drug to flourish....more »
    165. Kidney failure
     Total failure of the kidneys to filter waste...more »
    166. Krause syndrome
     A syndrome involving the abnormal development of the eye and cerebral portion of the brain. It most often occurs in premature infants or an infant from a multiple birth. It is believed to possibly result from intercurrent infections in the mother, placent...more »
    167. Kwashiorkor
     A malnutrition state that is produced by severe protein deficiency...more »
    168. Lipoid congenital adrenal hyperplasia
     A rare form of congenital adrenal hyperplasia where the early phase of adrenal cortisol production is defective which causes mineralocorticoid deficiency. Male pseudohermaphroditism is the main characteristic of this disorder....more »
    169. Lufyllin -- Teratogenic Agent
     There is evidence to indicate that exposure to Lufyllin (a bronchodilator) 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 ...more »
    170. MRXS-Christianson
     A very rare syndrome characterized mainly by mental retardation, mutism, facial anomalies, epilepsy and weak eye muscles. Males tended to have severe mental retardation whereas female carriers had mild or no mental retardation. Patients do eventually walk...more »
    171. Machupo virus
     A virus which is the cause of a form of hemorrhagic fever occurring in Bolivia...more »
    172. Mareck's disease -- nervous system
     A viral disease that affects poultry - it is very contagious and is a herpes virus. The virus tends to affect the nerves and cause tumors in internal organs. Poultry may be unable to lay eggs or may even die. Young birds are more susceptible than older bi...more »
    173. Mareck's disease -- visceral
     A viral disease that affects poultry - it is very contagious and is a herpes virus. The virus tends to affect the nerves and cause tumors in internal organs. Poultry may be unable to lay eggs or may even die. Young birds are more susceptible than older bi...more »
    174. Marek disease
     A viral disease that affects poultry - it is very contagious and is a herpes virus. The virus tends to affect the nerves and cause tumors in internal organs. Poultry may be unable to lay eggs or may even die. Young birds are more susceptible than older bi...more »
    175. Meningitis
     Dangerous infection of the membranes surrounding the brain....more »
    176. Mental retardation, Microcephaly, Epilepsy and Ataxia Syndrome
     A very rare syndrome characterized mainly by mental retardation, mutism, facial anomalies, epilepsy and weak eye muscles. Males tended to have severe mental retardation whereas female carriers had mild or no mental retardation. Patients do eventually walk...more »
    177. Mental retardation, X-linked -- craniofacial dysmorphology -- epilepsy -- ophthalmoplegia -- cerebellar atrophy
     A very rare syndrome characterized mainly by mental retardation, mutism, facial anomalies, epilepsy and weak eye muscles. Males tended to have severe mental retardation whereas female carriers had mild or no mental retardation. Patients do eventually walk...more »
    178. Mercury poisoning
     A type of heavy metal poisoning caused by excessive exposure to mercury....more »
    179. Mesenteric artery syndrome
     A rare condition where a part of the duodenum is compressed by the mesenteric artery which results in duodenal obstruction....more »
    180. Methylmalonic acidemia
    181. Methylmalonic acidemia, vitamin B12 responsive
     A rare genetic disorder characterized by the impaired ability to make a chemical called adenosylcobalamin. Adenosylcobalamin is a derivative of vitamin B12. The defect results a biochemical abnormality which affects the body's normal biochemical functioni...more »
    182. Methylmalonicaciduria, vitamin B12 unresponsive, mut 0
     A metabolic disorder whose severity is somewhat variable - most patients die within months of birth with survivors having neurological problems. The condition involves abnormal metabolism of vitamin B12 which doesn't respond to treatment using vitamin B12...more »
    183. Microphthalmis, isolated, with cataract 4
     A rare genetic eye disorder characterized by congenital cataracts (cloudy eye lens) and small eyes. The various types differ in the origin of the genetic defect. Type 4 involves a defect on chromosome 22q11.2-q13.1. Type 1 involves a defect on chromosome ...more »
    184. Microscopic lymphocytic colitis
     Microscopic lymphocytic colitis refers to inflammation of the colon that is only visible when the colon's lining is examined under a microscope. The appearance of the inner colon lining in microscopic colitis is normal by visual inspection during colonosc...more »
    185. Microvillus Inclusion Disease
     A rare, inherited, progressive intestinal disease where a defect in the intestinal wall results in severe diarrhea after birth....more »
    186. Multiple endocrine neoplasia
     A group of conditions that is characterised by the hyperplasia and hyperfunction of two or more glands of the endocrine system...more »
    187. Multiple endocrine neoplasia type 1
     Rare inherited disease causing tumors in multiple glands...more »
    188. Multiple endocrine neoplasia type 2
     Rare inherited disease causing tumors in multiple glands...more »
    189. Multiple endocrine neoplasia type 3
     Rare inherited disease causing tumors in multiple glands...more »
    190. Mumps
     An acute viral disease that causes the salivary glands to become swollen, sore and inflamed. Immunization had greatly reduced the incidence of this disease....more »
    191. Myocarditis
     Inflammation of the myocardium (muscle walls of the heart)...more »
    192. Nanophthalmos 2
     A dominantly inherited eye disorder linked to a defect on chromosome 11q23 which results in very small eyes. The condition is usually associated with an increased risk of glaucoma....more »
    193. Nanophthalmos 3
     A dominantly inherited eye disorder linked to a defect on chromosome 2q11-q14 which results in very small eyes. The condition is usually associated with an increased risk of glaucoma....more »
    194. Nephrogenic diabetes insipidus
     A rare inherited condition where the kidneys can't concentrate the urine sufficiently which results in excessive urination and thirst. The condition occurs because the kidneys are unable to respond to the antidiuretic hormone....more »
    195. Nephropathic cystinosis
     Cystinosis is a condition where excess amino acid cystine builds up to harmful levels in the body. The nephropathic form of cystinosis usually starts during infancy and can result in severe complications if untreated....more »
    196. Non infectious chronic diarrhea
     Diarrhoea that lasts for more than 2 weeks is considered persistent or chronic....more »
    197. Pancolitis
     Pancolitis is also known as ulcerative colitis which is an idiopathic chronicinflammatory disorder of the colon and rectum and involves the entire thickness of the colon....more »
    198. Pancreatitis
     Inflammation of the pancreas causing digestive complaints....more »
    199. Panhypopituitarism
     A rare condition where all pituitary hormones are absent or reduced. The condition may be congenital or acquired through such things as pituitary tumors. The pituitary gland regulates the activity of other endocrine glands as well as controlling growth. O...more »
    200. Parathyroid Cancer
     A condition that is characterised by malignancy that affects the parathyroid...more »
    201. Pemphigus neonatorum
     A group of conditions affecting the new born that resembles pemphigus...more »
    202. Periodic hyperlysinemia
     A rare genetic disorder where the body lacks enzymes to metabolize lysine which then causes a harmful builds up of lysine and ammonia in the body....more »
    203. Plant poisoning -- Castor bean (Ricinus communis)
     Ingestion of parts of the castor bean plant may cause severe symptoms....more »
    204. Plant poisoning -- Rosary pea (Abrus precatorious)
     Ingestion of parts of the Rosary pea plant may cause severe symptoms....more »
    205. Plant poisoning -- Water hemlock (Cicuta sp.)
     Ingestion of parts of the water pea plant may cause severe symptoms....more »
    206. Plant poisoning -- daffodil (Narcissus pseudonarcissus)
     Accidental ingestion of daffodils can result in gastrointestinal irritation which is usually mild but can be severe....more »
    207. Plant poisoning -- holly (Ilex sp.)
     Accidental ingestion of holly can result in gastrointestinal irritation which is usually mild but can be severe....more »
    208. Plant poisoning -- mistletoe (Phoradendron serotinum)
     Accidental ingestion of mistletoe can result in gastrointestinal irritation which is usually mild but can be severe....more »
    209. Plant poisoning -- pokeweed (Phytolacca Americana)
     Accidental ingestion of pokeweed can result in gastrointestinal irritation which is usually mild but can be severe....more »
    210. Polycystic kidney disease type 1
     A rare condition where cysts in the kidney grow and cause the kidney to become larger and reduce it's ability to function. PKD 1 is an autosomal dominant form of the disease and differs from PKD 2 in that it is more severe and is caused by a mutation in a...more »
    211. Polyendocrinopathy, immune dysfunction, and diarrhea, X-linked
     A rare condition involving autoimmune problems which can variably manifest as enteropathy (diarrhea), hemolytic anemia, and endocrine gland diseases such as diabetes mellitus and thyroid disease. Resistance to viral infections is poor. The condition is li...more »
    212. Progeria short stature pigmented nevi
     A very rare inherited disorder characterized by premature aging, short stature, and immune system deficiency. The type and severity of symptoms is variable....more »
    213. Propionic Acidemia
     A condition which is characterized by the excess of propionic acid and glycine in the blood resulting in acidaemia...more »
    214. Proximal tubulopathy -- diabetes mellitus -- cerebellar ataxia
     A very rare syndrome characterized mainly by diabetes, movement disorder and kidney abnormality. Death often occurs during childhood....more »
    215. Pseudohypoaldosteronism type 1, autosomal dominant
     A rare condition characterized by electrolyte disorders caused by the kidney's inability to respond to mineralocorticoids. Type 1 is differentiated from type II in that it involves sodium wasting. There are two forms of type 1: an autosomal recessive form...more »
    216. Pseudohypoaldosteronism type 1, autosomal recessive
     A rare condition characterized by electrolyte disorders caused by the kidney's inability to respond to mineralocorticoids. Type 1 is differentiated from type II in that it involves sodium wasting. There are two forms of type 1: an autosomal recessive form...more »
    217. Pseudomembranous Colitis
     Diarrhoeal illness caused by the bacteria Clostridium difficile, usually following a recent course of antibiotics and disruption of normal bowel bacteria...more »
    218. Psoriasis
     Psoriasis is an inflammatory skin condition where the defective immune system causes skin cells to grow rapidly. It affects a significant number of people. Arthritis, which can be severe, is associated with the psoriasis in up to a third of cases. Not all...more »
    219. Pulmonary embolism
     Blocked lung blood vessel often from a blood clot....more »
    220. Pulmonary hypertension
     Pulmonary hypertension refers to high blood pressure in the blood vessels that carry blood to the lungs. Blood pressure in other parts of the body is normal or sometimes even low. The condition may be caused by such things as lung conditions (e.g. emphyse...more »
    221. Pyloric stenosis
     Narrowed opening between stomach and intestines...more »
    222. RHYNS syndrome
     A rare syndrome characterized by eye, kidney and skeletal abnormalities as well as hypopituitarism....more »
    223. Renal tubulopathy -- diabetes mellitus -- cerebellar ataxia
     A very rare condition characterized by rapidly progressive diabetes, kidney disease and cerebellar ataxia. Symptoms develop during the first five years....more »
    224. Rieger anomaly -- partial lipodystrophy
     A very rare disorder characterized by short stature, low birth weight and loss of skin fat. SHORT is an acronym for short stature, hyperextensible joints and/or hernia, ocular depression, Reiger anomaly and teething delay. Additional symptoms are also var...more »
    225. Roseola infantum
     Contagious infant conditions...more »
    226. Rotavirus
     Diarrhea-causing virus in infants....more »
    227. Salmonella typhimurium infection
     An infection caused by bacteria from the Salmonella genus which can result in gastroenteritis, fever or may be asymptomatic. Infection is caused by consuming contaminated food or drinks....more »
    228. Sarcosporidiosis
     Infection with a protozoa called Sarcocystis. The condition is often asymptomatic. Infection usually occurs by eating raw infected meat....more »
    229. Secondary Bone Cancer
     Tumour development in bone as a result of spread from a primary malignant tumour from another body site (usually lung bronchus, breast and prostate)...more »
    230. Secondary Lactase Deficiency
     This form of lactase deficiency results from some sort of damage to the intestines either due to a disease or surgery. Some possible causes include untreated celiac disease, long-term use of antibiotics, giardiasis, carcinoid syndrome, HIV enteropathy, ga...more »
    231. Severe diarrhea
    232. Short Bowel Syndrome
     Disorder of shortened bowel usually from bowel surgery....more »
    233. Small bowel bacterial overgrowth syndrome
     The small bowel is a part of the digestive system. A healthy small bowel contains some bacteria but in bacterial overgrowth syndrome, there are an excessive number of bacteria. Abnormal small bowel muscle function is often associated with conditions such ...more »
    234. Staphylococcus aureus food poisoning
     Common type of food poisoning....more »
    235. Stevens-Johnson Syndrome
     A rare but serious condition involving inflammation and blistering of the skin and mucous membranes. It is believed to be an allergic reaction that can occur in response to some drugs or infectious diseases....more »
    236. Stroke
     Serious brain event from bleeding or blood clots....more »
    237. Sucrase-Isomaltase Deficiency
     A condition which is characterized by a deficiency of sucrase-isomaltase deficiency...more »
    238. Sucrase-isomaltase malabsorption, congenital
     A rare disorder where a congenital deficiency of an enzyme (sucrase-isomaltase) prevents the absorption of sucrose and isomaltose consumed in the diet....more »
    239. Sucrase-isomaltose malabsorption, congenital
     A rare disorder where a congenital deficiency of an enzyme (sucrase-isomaltase) prevents the absorption of sucrose and isomaltose consumed in the diet....more »
    240. Supraventricular Tachycardia
     A rapid heart rate, the cause of which originates above the ventricles....more »
    241. The Methylmalonic Acidemias
     A condition which is characterized by an excess of methylmalonic acid in the blood...more »
    242. Toni-Fanconi syndrome type 1
    243. Toxic megacolon
     It is a life threatening complication....more »
    244. Toxic mushrooms -- Gastrointestinal irritant
     Some mushrooms contain a chemical which cause gastrointestinal irritation. Mushroom species from this group include certain species of Agaricus, Amanita, Boletus, Entoloma, Gomphus, Lactarius, Omphalotus, Tricholoma, Tylopilus and Verpa....more »
    245. Toxic mushrooms -- Renal toxic (orelline)
     Some mushrooms (Amanita smithiana) contain chemicals (allenic norleucine, chlorocrotyglycine) which can cause kidney damage....more »
    246. Toxic mushrooms -- cyclopeptides
     Some mushrooms contain a toxic chemical called cyclopeptide which can cause primarily gastrointestinal symptoms if ingested. Most cases of mushroom poisoning in North America involve cyclopeptide-containing mushrooms. Mushroom species from this group incl...more »
    247. Trigeminal neuralgia
     Trigeminal neuralgia is a very painful inflammation of the nerve (trigeminal nerve) that delivers sensations to the face and "surface" of the eye....more »
    248. Type 2 diabetes
     Most common diabetes in adults, usually progressing slowly, mostly treated without insulin at diagnosis....more »
    249. Ulcerative colitis
     Ulcerative colitis (Colitis ulcerosa, UC) is a form of inflammatory bowel disease (IBD). Ulcerative colitis is a form of colitis, a disease of the intestine, specifically the large intestine or colon, that includes characteristic ulcers, or open sores, in...more »
    250. Vasopressin-resistant diabetes insipidus
     A condition which is characterised by normal renal filtration and solute excretion however there is a persistent hypotonic urine...more »
    251. Vibrio
     An organism of the genus Vibrio or other spiral motile organism...more »
    252. Vibrio infection -- Vibrio alginolyticus
     An infectious disease caused by a bacteria called Vibrio alginolyticus. This bacterium tends to cause ear and wound infections....more »
    253. Vibrio infection -- Vibrio damsela
     An infectious disease caused by a bacteria called Vibrio damsela. The nature and severity of symptoms can vary considerably depending on the type of infection caused - gastroenteritis, wound infection or septicemia. Wound infection is the most common dise...more »
    254. Vibrio infection -- Vibrio fluvialis
     An infectious disease caused by a bacteria called Vibrio fluvialis. The nature and severity of symptoms can vary considerably depending on the type of infection caused - gastroenteritis, wound infection or septicemia. Gastroenteritis is the most common di...more »
    255. Vibrio infection -- Vibrio furnissii
     An infectious disease caused by a bacteria called Vibrio furnissii. The nature and severity of symptoms can vary considerably depending on the type of infection caused - gastroenteritis, wound infection or septicemia. Gastroenteritis is the most common di...more »
    256. Vibrio infection -- Vibrio holisae
     An infectious disease caused by a bacteria called Vibrio holisae. The nature and severity of symptoms can vary considerably depending on the type of infection caused - gastroenteritis, wound infection or septicemia. Gastroenteritis is the most common dise...more »
    257. Vibrio infection -- Vibrio metschnikovii
     An infectious disease caused by a bacteria called Vibrio metschnikovii. The nature and severity of symptoms can vary considerably depending on the type of infection caused - gastroenteritis, wound infection or septicemia. Gastroenteritis is the most commo...more »
    258. Vibrio infection -- Vibrio mimicus
     An infectious disease caused by a bacteria called Vibrio mimicus. The nature and severity of symptoms can vary considerably depending on the type of infection caused - gastroenteritis, wound infection or septicemia. Gastroenteritis is the most common dise...more »
    259. Vibrio infection -- Vibrio parahaemolyticus
     An infectious disease caused by a bacteria called Vibrio parahaemolyticus. The nature and severity of symptoms can vary considerably depending on the type of infection caused - gastroenteritis, wound infection or septicemia. Gastroenteritis is the most co...more »
    260. Vibrio mimicus food poisoning
     Ingestion of food or water contaminated with a particular bacteria (Vibrio mimicus)....more »
    261. Vibrio vulnificus infection
     The infection by the vibrio vulnificus bacteria...more »
    262. Viral digestive infections
     Any virus that infects the gastrointestinal tract causing a medical condition...more »
    263. Viral gastroenteritis
     Virus causing gastroenteritis of digestive tract....more »
    264. Vomiting
    265. Waterhouse-Friederichsen syndrome
     A rare syndrome that occurs as complication of septicemia (often due to meningococcal or pneumococcal infection) and involves blood coagulation in blood vessels, adrenal gland hemorrhages and ultimately kidney failure....more »
    266. Whistling face syndrome
     A condition which is characterised by craniocarpotarsal dystrophy...more »
    267. Whistling face syndrome, recessive form
     A rare, recessively inherited syndrome characterized mainly by a characteristic "whistling" face and hand anomalies. The range of symptoms are variable....more »
    268. Whole-body acute irradiation -- gastrointestinal syndrome
     Tissue injury can result from exposure to radiation. The radiation dose, rate of dosing and tissues irradiated will determine the severity and type of symptoms. The effects may be chronic, delayed or acute. Gastrointestinal syndrome involves exposure of t...more »
    269. Wolfram Syndrome 2
     Wolfram Syndrome is a condition characterized by the association of diabetes insipidus, diabetes mellitus, optic atrophy and deafness. Type 2 is the result of a genetic defect and is similar to type 1 but there is no diabetes insipidus and patients tend t...more »
    270. Wolfram's disease
     A condition that is inherited and consists of multiple symptoms...more »
    271. Woodhouse Sakati syndrome
     A condition which consists of numerous symptoms such as diabetes, hypogonadism, deafness and mental retardation...more »

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