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Symptoms » Coordination problems » Glossary
 

Glossary for Coordination problems

Medical terms related to Coordination problems or mentioned in this section include:

  • 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency: A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Symptoms tend to be more severe in males who suffer progressive neurodegeneration whereas females tend to suffer mainly from developmental delay.
  • 3-alpha-hydroxyisobutyryl-CoA hydrolase deficiency: A metabolic disorder involving an enzyme deficiency which causes symptoms such as degeneration of the nervous system. The other features of the disorder are somewhat variable.
  • 3-methylglutaconic aciduria, type V: A rare genetic disorder where the body's cells are unable to make sufficient energy resulting in an accumulation in the body of 3-methylglutaconic acid.
  • 47,XXX syndrome: A genetic condition where females have an extra X chromosome in each of their cells. Normally female cells have two X chromosomes. This is not usually an inherited condition but a defect that occurs during cell division. Often the condition is asymptomatic.
  • ADD: Attention Deficit Disorder (ADD) is a mental and behavioral disorder characterized by behavioral problems such as hyperactivity, inattention, concentration difficulty, and other mental symptoms. The related description Attention Deficit Hyperactivity Disorder (ADHD) may be a more modern description of the disease.

    Misdiagnosis of ADD is a well-known controversy in the sense that cases of hyperactivity in children may be over-diagnosed. There is a tendency for parents to seek and doctors to prescribe the drug Ritalin even in cases where the diagnosis of ADD or ADHD may be incorrect. Alternative diagnoses include normal child behavior (i.e. just an active child), food intolerances, or other behavioral disorders (see misdiagnosis of ADD).

    On the other hand, ADD is under-diagnosed in adults, with a large number of adults having ADD without knowing it; see misdiagnosis of Adult ADD.

  • ARCA: A group of recessively inherited neurological disorders characterized mainly by cerebellar ataxia and usually with other additional abnormalities.
  • ARTS syndrome: A rare lethal syndrome characterized by deafness, optic atrophy and ataxia.
  • Abdominal Aneurysm: Dilatation of a section of the abdominal aorta, usually due to a weakness in the wall of the artery
  • Abetalipoproteinemia: A rare genetic disorder involving fat metabolism. The disorder is also known as Bassen-Kornzweig syndrome. Signs of the disease include acanthocytosis, little or no serum beta-lipoproteins and hypocholesterolemia. In severe cases, steatorrhea, ataxia, nystagmus, motor incoordination and retinitis pigmentosa may also occur.
  • Acanthamoeba infection: Infection with a microscopic, free-living ameba that is readily found in the environment - soil, air and water. Most people exposed to the ameba will not become infected but when infections do occur, they tend to affect the eyes, central nervous system or can cause widespread infection throughout the body.
  • Acanthamoeba infection of the central nervous system: Infection by an amoebic organism called Acanthamoeba. Infection usually occurs when the amoeba enters through a break in the skin or through the nose. Infection can be localized or systemic where it can involve the central nervous system and cause potentially fatal meningoencephalitis. Infection of the eye can occur by cleaning contact lenses in contaminated water.
  • Acanthocytosis: A rare disorder where most of the red blood cells are abnormal with spiny projections due to lipid abnormalities. The blood abnormality is seen in conditions such as abetalipoproteinemia, severe liver disease and severe malnutrition. Symptoms and prognosis depend on the underlying disorder.
  • 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.
  • Aceruloplasminemia: A rare genetic disorder characterized by a lack of the protein ceruloplasmin in the blood resulting in a buildup of iron in the liver, brain and pancreas. This in turn causes diabetes and degeneration of the neural system causing tremors and walking abnormalities.
  • Achrestic anemia: Achrestic anemia is a form of anemia similar to that caused by Vitamin B12 deficiency but it doesn't respond to treatment with Vitamin B12. The condition tends to progress slowly and can result in death if not treated. There are a variety of possible causes.
  • Acid-Base Imbalance: A disruption to the normal acid-base equilibrium in the body. There are four main groups of disorder involving an acid-base imbalance: respiratory acidosis or alkalosis and metabolic acidosis or alkalosis. Obviously the severity of symptoms is determined by the degree of imbalance.
  • Acoustic Neurinoma: A benign tumor of the 8th cranial nerve which lies in the tube connecting the inner ear to the brain.
  • Acoustic neuroma: A rare benign tumor that forms in the hearing canal. Can cause tinnitus, progressive hearing loss, headaches, facial numbness, papilledema, dizziness and an unsteady walk. Speaking and swallowing difficulty can occur in advanced stages. Also called acoustic neurilemoma, acoustic neurinoma and acoustic neurofibroma.
  • 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.
  • Acute Bokhoror: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. Death is common in the acute phase of the infection which can last from four days to four months.
  • Acute Chemical poisoning -- Varnish makers' and painters' Naptha: Varnish makers' and painters' Naptha is an ingredient used in certain pesticides. Exposure to the chemical can cause a range of symptoms depending on the level and route of exposure. Exposure can occur through inhalation, ingestion, the skin or eyes. Acute exposure involves a exposure over a short period of time whereas chronic exposure occurs over a longer period of time.
  • Acute Disseminated Encephalomyelitis: A type of encephalitis that usually follows an acute viral infection and involves an immune attack on myelin tissue which is part of the nervous system. Initial symptoms include fever, headache, vomiting and drowsiness followed by seizures, coma and paralysis. Often results in permanent neurological disorders.
  • Acute Pesticide poisoning -- xylene: Xylene is an ingredient used in certain insecticides. Exposure to the chemical can cause a range of symptoms depending on the level and route of exposure. Exposure can occur through inhalation, ingestion, the skin or eyes. Acute exposure involves a exposure over a short period of time whereas chronic exposure occurs over a longer period of time.
  • Acute VE: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. Death is common in the acute phase of the infection which can last from four days to four months.
  • Acute Viliuisk Encephalitis: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. Death is common in the acute phase of the infection which can last from four days to four months.
  • Acute Viliuisk Encephalomyelitis: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. Death is common in the acute phase of the infection which can last from four days to four months.
  • Acute Vilyuisk Encephalitis: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. Death is common in the acute phase of the infection which can last from four days to four months.
  • Acute Vilyuisk Encephalomyelitis: A brain disease caused by an unknown pathogen which is probably from the Picornavirus family of viruses. Mode of transmission is uncertain but genetic susceptibility may be involved. The incubation period appears to be an average of 15 years. The disease can be classified according to rate of progression: acute or subacute, slowly progressive and chronic. Death is common in the acute phase of the infection which can last from four days to four months.
  • Acute fulminant multiple sclerosis: Malignant Multiple Sclerosis, is a particularly aggressive form of the disease. Thankfully very rare, this highly aggressive form is defined by its swift and relentless decline to significant disability or even death, often within a few weeks or months after the onset of the initial attack. It is characterized by widespread and progressive cerebral white matter destruction or by severe pathological involvement of clinically strategic regions such as brainstem, resulting in bulbar paralysis.
  • Acute headache: Headache, or cephalgia, is defined as diffuse pain in various parts of the head, with the pain not confined to the area of distribution of a nerve.
  • Acute intermittent porphyria: A rare inherited metabolic disorder caused by a disturbed porphyrin metabolism resulting in increased production of porphyrin or its precursors. Symptoms include abdominal pain, photosensitivity and neurological disturbances such as seizures, coma, hallucinations and respiratory paralysis.
  • Acute leukaemia of ambiguous lineage: A term used to describe a type of leukemia (a blood cancer) where the leukemic cells cannot be determined as myeloid or lymphoid or where both types of cells are present.
  • Acute megacaryoblastic leukemia: A rare form of malignant bone marrow cancer involving the proliferation of immature precursors of blood cells. More specifically, it involves the rapid proliferation of megakaryoblasts (premature form of megakaryocytes).
  • Acute myeloblastic leukemia type 1: A form of blood cancer resulting in the rapid proliferation of immature blood cells (blast cells).
  • Acute myeloblastic leukemia type 2: A form of blood cancer resulting in the rapid proliferation of granulocytes and monocytes.
  • Acute myeloblastic leukemia type 3: A rare form of malignant bone marrow cancer involving the rapid proliferation of immature precursors of blood cells. Type 3 involves the proliferation of promyelocytes.
  • Acute myeloblastic leukemia type 4: A rare form of malignant bone marrow cancer involving the rapid proliferation of immature precursors of blood cells. Type 4 involves the rapid proliferation of myelocytes and monocytes.
  • Acute myeloblastic leukemia type 5: A rare form of malignant bone marrow cancer involving the proliferation of immature precursors of blood cells. Type 5 involves the rapid proliferation of monoblasts (immature precursors of monocytes) in particular.
  • Acute myeloblastic leukemia type 6: A rare form of malignant bone marrow cancer involving the rapid proliferation of immature precursors of blood cells. Type 6 involves the proliferation of the immature precursors of red blood cells called erythroblasts.
  • Acute myeloblastic leukemia type 7: A rare form of malignant bone marrow cancer involving the proliferation of immature precursors of blood cells. Type 7 involves the rapid proliferation of megakaryoblasts (premature form of megakaryocytes) in particular.
  • Acute myelocytic leukemia: A malignant cancer of blood-forming tissues resulting in a high number of immature leukocytes. Symptoms include soft bleeding gums, anemia, fatigue, fever, dyspnea, moderate splenomegaly, joint and bone pains and frequent infections. Also called acute granulocytic leukemia, acute myelogenous leukemia, acute nonlymphocytic leukemia, myeloid leukemia, splenomedullary leukemia, splenomyelogenous leukemia.
  • Acute myeloid leukaemia and myelodysplastic syndromes related to alkylating agent: The use of alkylating agents to treat cancer can result in leukemia in some patients.
  • Acute myeloid leukaemia and myelodysplastic syndromes related to topoisomerase type II inhibitor: The use of topoisomerase type II inhibitors to treat cancer can result in leukemia in some patients.
  • Acute myeloid leukaemia and myelodysplastic syndromes, therapy related: Certain cancer therapies can result in the development of leukemia in some patients. These therapies includes topoisomerase type II inhibitors and alkylating agents.
  • Acute myeloid leukemia: A form of rapidly progressing blood cancer resulting in the rapid proliferation of granulocytes and monocytes, red blood cells and platelets.
  • Acute myeloid leukemia, adult: A form of blood cancer resulting in the rapid proliferation of granulocytes and monocytes, red blood cells and platelets.
  • Acute non lymphoblastic leukemia: A form of rapidly progressing blood cancer resulting in the rapid proliferation of granulocytes and monocytes, red blood cells and platelets. It is one of the most common forms of leukemia in adults but can occur in children.
  • Acute vitamin A toxicity: Acute ingestion of vitamin A can cause symptoms. Symptoms usually only last for a day or two.
  • Adam and Eve poisoning: The Adam and Eve plant is a herb with heart-shaped leaves found in Europe. The plant contains a poisonous chemical called calcium oxalate crystals which can cause a variety of symptoms if ingested. Eye exposure can also cause symptoms due to the abrasive nature of the toxic chemical. Ingestion of the plant generally causes severe mouth pain. Skin exposure usually only causes minor, short-lived skin irritation.
  • Adenosine triphosphatase deficiency, anaemia due to: Deficiency of a chemical (adenosine triphosphate) resulting in anemia.
  • Adhd: Attention Deficit Hyperactivity Disorder (ADHD) is a mental and behavioral disorder characterized by behavioral problems such as hyperactivity, inattention, concentration difficulty, and other mental symptoms. Typically, ADHD and associated hyperactivity is known as a childhood disorder, although ADD/ADHD in adults is known to be under-diagnosed. It is distinguished from Attention Deficit Disorder (ADD) which has a reduced focus on hyperactivity type symptoms.
  • 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.
  • Adrenal crisis: A potentially fatal condition where the adrenal cortex slows or stops functioning resulting in reduced glucocorticoids, decreased extracellular fluid volume and hyperkalemia. Symptoms include shock, coma, low blood pressure, weakness and loss of vasomotor tone. Also called addisonian crisis.
  • 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.
  • Adrenal gland symptoms: Symptoms affecting the adrenal glands
  • Adrenal hypertension: Adrenal hypertension is high blood pressure caused by adrenal gland problems. For example, an adrenal tumor can cause excessive production of aldosterone which in turn causes salt-retention and high blood pressure. Severity of symptoms varies depending on the underlying cause.
  • Adrenal hypofunction: A condition which is characterized by a lack of production of hormones from the adrenal gland.
  • Adult Panic-Anxiety Syndrome: A psychiatric disorder involving anxiety and panic attacks that occur for no obvious reason.
  • Adult progressive spinal muscular atrophy, Aran Duchenne type: A group of inherited motor neuron diseases involving progressive muscle weakness, wasting and paralysis due to degeneration of motor neurons in the spinal cord. Muscle weakness and wasting usually starts in the hands and may gradually spread to other muscle groups.
  • Adult-onset ALD: Form of ALD in adults.
  • 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.
  • Aerotitis syndrome: Trauma to the blood vessels in the ears caused by rapid changes in atmospheric pressure. Blockage of the Eustachian tube in the ear prevents equalization of air pressure and a vacuum develops inside the ear. Yawning or chewing can sometimes alleviate symptoms by opening up the Eustachian tube.
  • Agenesis of the corpus callosum: Congenital absence of connective part of the brain.
  • Aging brain syndrome: Aging processes in the brain can cause various psychological and neurological symptoms.
  • Air embolism: A condition where an air bubble enters the cardiovascular system (via injection, intravenous therapy, surgery or puncture wound) and obstructs the blood flow.
  • Al Murrah-induced lead poisoning: Al Murrah is a folk remedy used mainly by Saudi Arabian people to treat problems such as stomach pain, diarrhea and colic. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
  • Alarcon-induced lead poisoning: Alarcon is a folk remedy used mainly by Mexican people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
  • Albayaidle-induced lead poisoning: Albayaidle is a folk remedy used mainly by Mexican and Central American people to treat digestive or stomach problems such as vomiting and colic. It is also used to treat apathy and lethargy. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
  • Albayalde-induced lead poisoning: Albayalde is a folk remedy used mainly by Mexican and Central American people to treat digestive or stomach problems such as vomiting and colic. It is also used to treat apathy and lethargy. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
  • Alcohol abuse: Excessive alcohol as a symptom of other conditions
  • Alcohol drinking: The consumption of a drink containing alcohol. Alcohol consumption can cause varying degrees of impairment depending on the amount consumed. Consuming very large amounts of alcohol can lead to death.
  • Alcohol-Induced Disorders: Disorders caused by excessive alcohol consumption. The symptoms are variable depending on the disorder involved. Some of the disorders are: alcohol abuse, alcohol dependence, alcohol intoxication, alcohol withdrawal, alcohol intoxication delirium, alcohol withdrawal delirium, alcohol-induced persisting dementia, alcohol-induced persisting amnestic disorder, alcohol-induced psychotic disorder, alcohol-induced mood disorder, alcohol-induced anxiety disorder, alcohol-induced sexual dysfunction, alcohol-induced sleep disorder, liver damage, liver cancer and esophageal cancer.
  • Alcohol-induced hypertension: Alcohol-induced hypertension is high blood pressure caused by excessive drinking of alcohol.
  • Alcoholic Neuropathy: Neurological changes due to nerve damage from long-term alcohol consumption
  • Alcoholic cerebellar degeneration: cerebellar degeneration which occurs in alcoholics
  • Alcoholic intoxication: The excessive consumption of alcohol can have toxic effects on the body and can ultimately result in death in severe cases.
  • Alexander Syndrome: Brain myelin disorder causing mental degeneration.
  • Alpers Syndrome: A rare syndrome characterized by liver disease, seizures and progressive, episodic psychomotor retardation.
  • Alpha-Mannosidosis: A rare condition which is characterized by a lysosomal storage defect.
  • Alpha-N-acetylgalactosaminidase deficiency, Type II: A very rare inherited metabolic disorder where deficiency of an enzyme (alpha-N-acetylgalactosaminidase) causes glycoplids to accumulate in body tissues and result in various symptoms. Type 2 occurs during the second or third decade of life and is milder than type I and doesn't involve neurological degeneration.
  • Alpha-ketoglutarate dehydrogenase deficiency: A metabolic disorder characterized by a deficiency of Alpha-ketoglutarate dehydrogenase which results in high levels of oxoglutaric acid in the urine as well as other severe symptoms.
  • Alpine syndrome: A condition that occurs in some people who go to low altitude winter resorts (1500 metres). It tends to mostly affect people who have been fasting when they arrive.
  • Alternating Hemiplegia: Episodes of one-sided paralysis.
  • Alzheimer disease 10: An inherited form of Alzheimer's. Type 10 is caused by a genetic defect on chromosome 10p13.
  • Alzheimer disease 12: An inherited form of Alzheimer's. Type 12 is caused by a genetic defect on chromosome 8p12-q22.
  • Alzheimer disease 13: An inherited form of Alzheimer's disease that is linked to a defect on chromosome 1q21. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease 14: An inherited form of Alzheimer's disease that is linked to a defect on chromosome 1q25. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease 15: An inherited form of Alzheimer's disease that is linked to a defect on chromosome 3q22-q24. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease 16: Alzheimer disease 16 (late-onset) is a form of Alzheimer's disease that is linked to a defect on chromosome Xq21.3. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease 2, late-onset: Alzheimer disease 2 (late-onset) is a form of Alzheimer's disease that is linked to a defect on chromosome 19q13.2. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease 3, (early-onset Alzheimer disease): Alzheimer disease 3 is an early-onset form of Alzheimer's disease that is linked to a defect on chromosome 14q24.3. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease 5: An inherited form of Alzheimer's. Type 5 has a late onset and is caused by a genetic defect on chromosome 12p11.
  • Alzheimer disease 6: A genetic form of Alzheimer's. Type 6 has a late onset and is caused by a genetic defect on chromosome 10q24.
  • Alzheimer disease 7: An inherited form of Alzheimer's. Type 7 is caused by a genetic defect on chromosome 10p13.
  • Alzheimer disease 8: An inherited form of Alzheimer's. Type 8 is caused by a genetic defect on chromosome 20p.
  • Alzheimer disease 9: A genetic form of Alzheimer's. Type 9 has a late onset and is caused by a genetic defect on chromosome 19p13.2.
  • Alzheimer disease, early-onset, with cerebral amyloid angiopathy: An early-onset form of Alzheimer's disease that is linked to a defect on chromosome 21q21. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease, familial, 1: An inherited form of Alzheimer's disease that is linked to a defect on chromosome 21q. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease, familial, 11: An inherited form of Alzheimer's disease that is linked to a defect on chromosome 9p22.1. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease, familial, 3, with spastic paraparesis and apraxia: This form of Alzheimer's is an early-onset form of Alzheimer's that is linked to a defect on chromosome 14q24.3. It is characterized by features which are atypical for Alzheimer's - spastic paraparesis which occurs before the dementia symptoms and apraxia. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease, familial, 3, with spastic paraparesis and unusual plaques: This form of Alzheimer's is an early-onset form of Alzheimer's that is linked to a defect on chromosome 14q24.3. It is characterized by features which are atypical for Alzheimer's - spastic paraparesis which occurs before the dementia symptoms and unusual plaques in the brain. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer disease, familial, 4: An inherited form of Alzheimer's disease that is linked to a defect on chromosome 1q31-q42. Alzheimer's disease is a progressive disorder involving degeneration of the brain. The disease mainly affects brain functions involving thinking, memory, personality and behaviour.
  • Alzheimer's disease: A progressive degenerative disease of the brain of unknown cause
  • Ambien overdose: Ambien is a prescription drug mainly used to treat insomnia. Excessive doses of the drug can result in various symptoms and even death in severe cases.
  • Amnesic shellfish poisoning: Rare shellfish poisoning sometimes causing amnesia.
  • Amphetamine abuse: Use of the stimulant drugs known as amphetamines or "speed"
  • Amphetamine-induced hypertension: Amphetamine-induced hypertension is high blood pressure caused by use of amphetamines. Patients with an existing history of hypertension may suffer further blood pressure increases while taking amphetamines and this can be serious. Severity of symptoms varies amongst patients depending on their susceptibility, underlying health and duration of amphetamine use.
  • Amyloid Neuropathies: A peripheral nerve disorder caused by abnormal amyloid deposits in the nerves. Sensory, autonomic or motor nerves may be affected. The degree of nerve involvement, and hence symptoms, are variable.
  • Amyloidosis, oculoleptomeningeal: Amyloidosis involves the abnormal deposit of a substance called amyloid in various parts of the body. In this particular type, the amyloid deposits in the leptomeningeal blood vessels, brainstem, spinal cord and eye causing central nervous system dysfunction, brain hemorrhages and vision impairment.
  • Amyotrophic lateral sclerosis: A degenerative motor neuron disease marked by weakness and wasting of the muscles which starts at the hands and legs and spreads to the rest of the body. Death occurs in 2 to 5 years. Also called Lou Gehrig's disease or wasting palsy.
  • Amyotrophic lateral sclerosis, type 6: An inherited disorder involving progressive degeneration of motor neurons which results in muscle weakness and wasting. Type 6 is caused by a defect on chromosome 16q12.
  • Anaemia, sideroblastic, X-linked -- ataxia: A very rare inherited disorder characterized by mild anemia and early onset neurological motor symptoms. The neurological symptoms tend to be relatively stable or slowly progressive with only occasional dependence on crutches or wheelchairs.
  • Anchovy poisoning (clupeotoxin): Some anchovies contain toxins (Clupeotoxin) which can be poisonous to humans if eaten. Heat does not destroy the toxin and there is still uncertainty as to the origin of the toxin. The toxin appears to be present in higher concentrations in summer and is believed to be possible linked to the consumption of toxic food in its food web. The size and age of the anchovy does not appear to be related to the toxicity. The anchovies are found in coastal waters off Africa and the Caribbean, Indian and Pacific Oceans.
  • Ancylostoma duodenale: An infestation with Ancylostoma duodenale which is a parasitic hookwork whichcan cause serious disease in humans - usually occurs in people who work barefoot in damp soil. The hookworms suck blood from the intestines of the host which can result in anemia if there is a large number of worms.
  • Anemia: Reduced red blood cells in the blood
  • Anemia of pregnancy: Anemia of pregnancy is anemia that occurs during pregnancy. Women's bodies have a greater demand for iron during pregnancy and if intake is not sufficient, anemia can result. Anemia in pregnant women can lead to infant problems such as premature birth, fetal death, retarded growth and other problems.
  • Anemia, Hemolytic, Warm Antibody: A rare autoimmune condition where the body's defense system attacks and destroys red blood cells. The onset of the condition is triggered by temperatures 37ºC or higher. The severity of the disorder is variable.
  • Anemia, Iron-Deficiency: A lack of fully functioning red blood cells due to a deficiency of iron. The iron allows the body to make hemoglobin in red blood cells which in turn allows the red blood cell to carry oxygen.
  • Anemia, Refractory, with Excess of Blasts: A bone marrow disease which results in insufficient red blood cells in the blood (anemia). The prognosis is poor with death usually occurring within a couple of years. There are two types: type 1 refers to cases where the level of blasts is less than 10% and type 2 refers to cases where the level of blasts is 10-20%. When too many immature blood cells (blasts) are produced by the bone marrow, the condition may progress to acute myeloid leukemia - occurs in about a quarter of cases in type 1 and a third of cases in type 2.
  • Anemia, Refractory, with Excess of Blasts, type 1: A bone marrow disease which results in insufficient red blood cells in the blood (anemia). The prognosis is poor with death usually occurring within a couple of years. Type 1 refers to cases where the level of blasts is less than 10% and type 2 refers to cases where the level of blasts is 10-20%. When too many immature blood cells (blasts) are produced by the bone marrow, the condition may progress to acute myeloid leukemia - occurs in about a quarter of cases in type 1.
  • Anemia, Refractory, with Excess of Blasts, type 2: A bone marrow disease which results in insufficient red blood cells in the blood (anemia). The prognosis is poor with death usually occurring within a couple of years. Type 1 refers to cases where the level of blasts is less than 10% and type 2 refers to cases where the level of blasts is 10-20%. When too many immature blood cells (blasts) are produced by the bone marrow, the condition may progress to acute myeloid leukemia - occurs in about a third of cases in type 2.
  • Anemia, hypochromic microcytic: A blood disorder where red blood cells are too small and lack sufficient iron. It can be inherited or caused by insufficient iron in the diet or from a genetic disorder.
  • Anemias, Sideroblastic: Sideroblastic anemias are a group of rare blood disorders where the bone marrow is unable to produce normal red blood cells. The body has enough iron but the red blood cells are unable to utilize it in a normal manner and anemia results. The red blood cells become overloaded with iron and are unable to carry out their normal functions. Some forms of sideroblastic anemia are inherited but most tend to be acquired due to such things as exposure to toxins and certain drugs, leukemia, inflammatory conditions such as rheumatoid arthritis and nutritional deficiencies (e.g. copper and pyridoxine deficiency). Inherited forms usually appear in childhood whereas acquired forms usually occur in adulthood.
  • Angelman syndrome: A rare genetic disorder characterized by a puppet-like gait, fits of laughter and characteristic facial features.
  • 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 but then often lose this ability by the age of 10 years. Female carriers tend to have mild symptoms and males have severe symptoms - symptoms are variable to some degree.
  • Angina pectoris: severe chest pain due to ischemia
  • Aniridia ataxia renal agenesis psychomotor retardation: A rare genetic disorder characterized by missing irises of the eye, ataxia, psychomotor retardation and abnormally kidneys.
  • Anorexia Nervosa: A disorder where a distorted sense of body image leads to self-starvation to the point of death in some cases.
  • Anxiety disorder: A mental condition that is characterized by anxiety and avoidance behaviours
  • Anxiety-tension syndrome: Anxiety associated with physical symptoms such as tense muscles and fatigue.
  • Aorta-pulmonary artery fistula: An abnormal opening or connection between the aorta and the main pulmonary artery. It can occur through a traumatic penetrating injury or may be a complication of surgery. Severe cases can lead to heart failure.
  • Aortic valve disease: Disease of the heart's aortic valve
  • Aortic valves stenosis of the child: A birth defect where the aortic valve is abnormally narrow or unable to fully open. Depending on the degree of narrowing, the symptoms may range from severe to asymptomatic.
  • Aplastic anemia: A blood disorder where the bone marrow produces insufficient new blood cells.
  • Apple seed poisoning: Apple seeds contain a toxic chemical called amygdalin which can cause serious symptoms if eaten in large quantities. Hospital admission is recommended if more than 50 apple seeds have been consumed.
  • Apraxia: A disorder of skilled movement not due to tremors, weakness, akinesia or abnormal tone or posture.
  • Arachnodactyly -- ataxia -- cataract -- aminoaciduria -- mental retardation: A rare syndrome characterized mainly by congenital cataracts, ataxia, mental retardation, abnormal amino acid metabolism and long, thin fingers.
  • Arachnoid Cysts: A rare disorder involving a fluid-filled cysts on the arachnoid membrane which is one of the thin layers of tissue that form a membrane which covers the spinal cord and brain. The type and severity of symptoms is determined by the size and location of the cyst.
  • Arachnoiditis: A progressive disorder where the arachnoid membrane becomes inflamed and the brain and spinal cord may also become inflamed.
  • Arctic bearded seal poisoning: The Arctic Bearded seal is often used as a food source by the arctic inhabitants. Eating the liver and kidneys of the arctic bearded seal can result in a Vitamin A overdose which can cause serious symptoms and even death in extreme cases. It is believed that eating more than 100-250 grams of the seal liver can result in human death.
  • Arginase deficiency: A very rare urea cycle disorder caused by a deficiency of the enzyme (arginase) needed to convert ammonia to the urea which can then be removed in the urine. The condition leads to excess build-up of ammonia in the body which is toxic to the nervous system.
  • Argininosuccinase lyase deficiency, late onset: A rare inherited urea cycle disorder caused by lack of enzymes (argininosuccinase lyase) needed to turn ammonia into urea resulting in excess ammonia in the body. The late onset form of the condition tends to start later in life as there is some level of activity by the defective enzyme. The condition tends to be less severe and can be triggered by a change in diet, illness or some other stress on the body.
  • Arizona Bark Scorpion poisoning: A bite from the Arizona Bark scorpion contains chemicals toxic to the nerve system and can cause serious, life-threatening symptoms.
  • Arnold-Chiari Malformation (Type 1): A rare malformation where the base of the brain enters into the upper spinal canal.
  • Arnold-Chiari malformation type 2: A rare malformation where the base of the brain enters into the upper spinal canal. The extent of the deformity is greater in type 2 than type 1 and hence the symptoms are more severe and are often associated with a myelomeningocele (opening of the spine and spinal cord).
  • Arnold-Chiari malformation type 3: An extremely rare malformation where the base of the brain enters into the upper spinal canal. Type 3 involves the herniation of brain or brain stem tissue out of the back of the neck or head. The condition generally has a poor prognosis.
  • Arnold-Chiari malformation type 4: Arnold-Chiari malformation is a rare malformation where the base of the brain enters into the upper spinal canal. Type 4 actually involves a lack of development of a portion of the base of the brain (cerebellum). The prognosis is very poor with death often occurring during infancy.
  • Arrhythmogenic right ventricular dysplasia: A rare heart muscle disease where the muscle tissue of the right ventricle of the heart is replaced by fibrous or fatty tissue which affects the ability of the heart to pump blood.
  • Arrhythmogenic right ventricular dysplasia, familial, 1: A rare heart muscle disease where the muscle tissue of the right ventricle of the heart is replaced by fibrous or fatty tissue which affects the ability of the heart to pump blood. Some patients are asymptomatic and whereas others experience symptoms and occasionally sudden death can occur. Type 1 is linked to chromosome 14q23-q24 (TGFB3 gene).
  • Arrhythmogenic right ventricular dysplasia, familial, 10: A rare heart muscle disease where the muscle tissue of the right ventricle of the heart is replaced by fibrous or fatty tissue which affects the ability of the heart to pump blood. Some patients are asymptomatic and whereas others experience symptoms and occasionally sudden death can occur. Type 10 is linked to chromosome 18q12.1-q12 (DSG2 gene).
  • Arrhythmogenic right ventricular dysplasia, familial, 11: A rare heart muscle disease where the muscle tissue of the right ventricle of the heart is replaced by fibrous or fatty tissue which affects the ability of the heart to pump blood. Some patients are asymptomatic and whereas others experience symptoms and occasionally sudden death can occur. Type 11 is linked to chromosome 18q12.1 (DSC2 gene).
  • Arrhythmogenic right ventricular dysplasia, familial, 12: A rare heart muscle disease where the muscle tissue of the right ventricle of the heart is replaced by fibrous or fatty tissue which affects the ability of the heart to pump blood. Some patients are asymptomatic and whereas others experience symptoms and occasionally sudden death can occur. Type 12 is linked to chromosome 17q21 (JUP gene).
  • Arrhythmogenic right ventricular dysplasia, familial, 2: A rare heart muscle disease where the muscle tissue of the right ventricle of the heart is replaced by fibrous or fatty tissue which affects the ability of the heart to pump blood. Some patients are asymptomatic and whereas others experience symptoms and occasionally sudden death can occur. Type 2 is linked to chromosome 1q42.1-q43 (RYR2 gene).
  • Arrhythmogenic right ventricular dysplasia, familial, 3: A rare heart muscle disease where the muscle tissue of the right ventricle of the heart is replaced by fibrous or fatty tissue which affects the ability of the heart to pump blood. Some patients are asymptomatic and whereas others experience symptoms and occasionally sudden death can occur. Type 3 is linked to chromosome 14q12-q22.
  • Arrhythmogenic right ventricular dysplasia, familial, 4: A rare heart muscle disease where the muscle tissue of the right ventricle of the heart is replaced by fibrous or fatty tissue which affects the ability of the heart to pump blood. Some patients are asymptomatic and whereas others experience symptoms and occasionally sudden death can occur. Type 4 is linked to chromosome 2q32.1-q32.3.
  • Arrhythmogenic right ventricular dysplasia, familial, 5: A rare heart muscle disease where the muscle tissue of the right ventricle of the heart is replaced by fibrous or fatty tissue which affects the ability of the heart to pump blood. Some patients are asymptomatic and whereas others experience symptoms and occasionally sudden death can occur. Type 5 is linked to chromosome 3p23.
  • Arrhythmogenic right ventricular dysplasia, familial, 6: A rare heart muscle disease where the muscle tissue of the right ventricle of the heart is replaced by fibrous or fatty tissue which affects the ability of the heart to pump blood. Some patients are asymptomatic and whereas others experience symptoms and occasionally sudden death can occur. Type 6 is linked to chromosome 10p14-p12.
  • Arrhythmogenic right ventricular dysplasia, familial, 7: A rare heart muscle disease where the muscle tissue of the right ventricle of the heart is replaced by fibrous or fatty tissue which affects the ability of the heart to pump blood. Some patients are asymptomatic and whereas others experience symptoms and occasionally sudden death can occur. Type 7 is linked to chromosome 10q22-3.
  • Arrhythmogenic right ventricular dysplasia, familial, 8: A rare heart muscle disease where the muscle tissue of the right ventricle of the heart is replaced by fibrous or fatty tissue which affects the ability of the heart to pump blood. Some patients are asymptomatic and whereas others experience symptoms and occasionally sudden death can occur. Type 8 is linked to chromosome 6p24 (DSP gene).
  • Arrhythmogenic right ventricular dysplasia, familial, 9: A rare heart muscle disease where the muscle tissue of the right ventricle of the heart is replaced by fibrous or fatty tissue which affects the ability of the heart to pump blood. Some patients are asymptomatic and whereas others experience symptoms and occasionally sudden death can occur. Type 9 is linked to chromosome 12p11 (PKP2 gene).
  • Arteriosclerosis Obliterans: Arteriosclerosis that results in the narrowing and gradual blockage of the artery. Arteriosclerosis involves the deposition of cholesterol plaques and other material on the inside of the artery walls. The symptoms will depend on the location of the arteries affected and how severe the blockage is.
  • Aspartylglucosaminidase deficiency: A rare glycoprotein metabolism disorder caused by a deficiency of an enzyme called aspartylglucosaminidase. Patients tend to develop normally during the first few years of life and development continues slowly until adolescence when mental retardation becomes progressively worse.
  • Aspartylglucosaminuria: A rare glycoprotein metabolism disorder caused by a deficiency of an enzyme called aspartylglucosaminidase. Patients tend to develop normally during the first few years of life and development continues slowly until adolescence when mental retardation becomes progressively worse.
  • Aspartylglycosaminuria: A rare glycoprotein metabolism disorder caused by a deficiency of an enzyme called aspartylglucosaminidase. Patients tend to develop normally during the first few years of life and development continues slowly until adolescence when mental retardation becomes progressively worse.
  • Asperger Syndrome, Susceptibility to, 1: Asperger Syndrome is considered to be a mild form of autism and manifests in symptoms such as problems with social interactions and repetitive behavior patterns and interests. Language and cognition skills are considerable less affected than in autism. Researchers have discovered that there are a number genetic anomalies linked to an increased risk of developing Asperger Syndrome. Type 1 is linked to a defect on chromosome 3q25-q27.
  • Asperger Syndrome, Susceptibility to, 2: Asperger Syndrome is considered to be a mild form of autism and manifests in symptoms such as problems with social interactions and repetitive behavior patterns and interests. Language and cognition skills are considerable less affected than in autism. Researchers have discovered that there are a number genetic anomalies linked to an increased risk of developing Asperger Syndrome. Type 2 is linked to a defect on chromosome 17p13.
  • Asperger Syndrome, Susceptibility to, 3: Asperger Syndrome is considered to be a mild form of autism and manifests in symptoms such as problems with social interactions and repetitive behavior patterns and interests. Language and cognition skills are considerable less affected than in autism. Researchers have discovered that there are a number genetic anomalies linked to an increased risk of developing Asperger Syndrome. Type 3 is linked to a defect on chromosome 1q21-q22.
  • Asperger Syndrome, X-linked, Susceptibility to, 1: Asperger Syndrome is considered to be a mild form of autism and manifests in symptoms such as problems with social interactions and repetitive behavior patterns and interests. Language and cognition skills are considerable less affected than in autism. Researchers have discovered that there are a number genetic anomalies linked to an increased risk of developing Asperger Syndrome. X-linked type 1 is linked to a defect on chromosome Xq13.
  • Asperger Syndrome, X-linked, Susceptibility to, 2: Asperger Syndrome is considered to be a mild form of autism and manifests in symptoms such as problems with social interactions and repetitive behavior patterns and interests. Language and cognition skills are considerable less affected than in autism. Researchers have discovered that there are a number genetic anomalies linked to an increased risk of developing Asperger Syndrome. X-linked type 1 is linked to a defect on chromosome Xp22.3.
  • Asperger syndrome: A neuropsychiatric disorder mainly involving the inability to understand and becoming involved in social interaction.
  • Asthenopia: Asthenopia or eye strain refers to general eye symptoms such as vision blurring, eye pain, eye weakness, eye fatigue and headaches which can result from overuse of the eyes or uncorrected vision problems.
  • Astrocytoma: A malignant tumour of the nervous system composed of astrocytes.
  • Asymmetric septal hypertrophy: A disease of the heart muscle characterized by increased thickness of the wall of the heart ventricle which affects the hearts function.
  • Ataxia: Failure of muscular coordination
  • Ataxia -- apraxia -- mental retardation, X-linked: A rare X-linked syndrome characterized mainly by ataxia, apraxia and mental retardation. The symptoms are generally nonprogressive.
  • Ataxia -- diabetes -- goiter -- gonadal insufficiency: A rare disorder characterized by diabetes, goiter, insufficient hormone production by the gonads and progressive ataxia.
  • Ataxia -- oculomotor apraxia, type 1: A nerve disorder which affects the motor nerves and results in movement problems which includes the eyes. Gait problems are usually the first symptom and this is followed by speaking difficulty, intention tremor and then eye movement problems.
  • Ataxia Telangiectasia: A rare inherited childhood disorder involving progressive degeneration of the nervous system.
  • Ataxia deafness reardon type: A rare syndrome observed in a Kuwati family characterized by ataxia, deafness and mental retardation.
  • Ataxia in children: Ataxia in children is an abnormal walk or gait in a child.
  • Ataxia spastic congenital miosis: A rare, dominantly inherited disorder characterized mainly by ataxia, spasticity and small pupils that respond poorly to light.
  • Ataxia tapetoretinal degeneration: Conditions involving incoordination and an eye anomaly.
  • Ataxia with Vitamin E Deficiency: A rare disorder where a genetic disorder results in impaired vitamin E deficiency which in turn causes progressive neurological problems such as ataxia.
  • Ataxia, episodic -- vertigo -- tinnitus -- myokymia: A rare genetic disorder characterized by episodes of incoordination and unsteadiness as well as tinnitus and vertigo. Stress, exhaustion, sudden movements and exertion may trigger the episodes. It is caused by a defect on chromosome 1q42.
  • Ataxia, spastic with congenital miosis: A rare disorder characterized by movement problems of the limbs as well as an impaired pupil reaction to light (miosis).
  • Ataxia, spastic, 3, autosomal recessive: A recessively inherited disorder characterized mainly by spasticity and ataxia.
  • Ataxia-deafness syndrome: A rare syndrome characterized by the association of ataxia with deafness.
  • Ataxia-oculomotor apraxia syndrome: A nerve disorder which affects the motor nerves and results in movement problems which includes the eyes. Gait problems are usually the first symptom and this is followed by speaking difficulty, intention tremor and then eye movement problems.
  • Ataxic gait: impairment of the ability to coordinate the movements required for normal ambulation which may result from impairments of motor function or sensory feedback
  • Atrial Fibrillation, Familial 2: A rare inherited condition where abnormal electrical activity in the heart causes it to have a fast and irregular beat. The condition may go unnoticed or may cause stroke or sudden death in some cases. Type 2 is linked to a genetic defect on chromosome 6q14-q16 and is inherited in an autosomal dominant manner. Symptoms tend to occur in episodes initially and then becomes chronic with increased age.
  • Atrial Fibrillation, Familial 3: A rare inherited condition where abnormal electrical activity in the heart causes it to have a fast and irregular beat. The condition may go unnoticed or may cause stroke or sudden death in some cases. Type 3 is linked to a genetic defect on chromosome 11p15.5 and is inherited in an autosomal dominant manner.
  • Atrial Fibrillation, Familial 4: A rare inherited condition where abnormal electrical activity in the heart causes it to have a fast and irregular beat. The condition may go unnoticed or may cause stroke or sudden death in some cases. Type 4 is linked to a genetic defect on chromosome 21q22.
  • Atrial Fibrillation, Familial 5: A rare inherited condition where abnormal electrical activity in the heart causes it to have a fast and irregular beat. The condition may go unnoticed or may cause stroke or sudden death in some cases. Type 5 is linked to a genetic defect on chromosome 4q2.
  • Atrial Fibrillation, Familial 6: A rare inherited condition where abnormal electrical activity in the heart causes it to have a fast and irregular beat. The condition may go unnoticed or may cause stroke or sudden death in some cases. Type 6 is linked to a genetic defect on chromosome 1p36.2 and is inherited in an autosomal dominant manner.
  • Atrial Fibrillation, Familial 7: A rare inherited condition where abnormal electrical activity in the heart causes it to have a fast and irregular beat. The condition may go unnoticed or may cause stroke or sudden death in some cases. Type 7 is linked to a genetic defect on chromosome 12p13 and is inherited in an autosomal dominant manner.
  • Atrial Fibrillation, Familial 8: A rare inherited condition where abnormal electrical activity in the heart causes it to have a fast and irregular beat. The condition may go unnoticed or may cause stroke or sudden death in some cases. Type 8 is linked to a genetic defect on chromosome 16q22 and is inherited in an autosomal dominant manner. Symptoms tend to occur in episodes initially and then becomes chronic with increased age.
  • Atrial arrhythmia: Arrhythmia arising in the atrium.
  • Atrial fibrillation, familial 1: A dominantly inherited condition where abnormal electrical activity in the heart causes it to have a fast and irregular beat. The condition may go unnoticed or may cause stroke or sudden death in some cases.
  • Atrial flutter: Heart arrhythmia where atria beat more often than ventricles
  • Atrial myxoma, familial: An atrial myxoma benign tumor that develops in the wall that separates the two upper chambers of the heart. The familial form of the condition also involves tumors in other parts of the body such as the skin, both heart atria or the heart ventricles.
  • Attention Deficit Hyperactivity Disorder: Behavioral disorder with hyperactivity and/or inattention.
  • Attention Deficit-Hyperactivity Disorder, Susceptibility to, 1: ADHD or attention deficit hyperactivity disorder is a common neurobehavioral developmental disorder that usually occurs in childhood and can continue into adulthood. Researchers have discovered a number of genes linked to an increased susceptibility to ADHD. Type 1 is linked to a defect on chromosome 16p13.
  • Attention Deficit-Hyperactivity Disorder, Susceptibility to, 2: ADHD or attention deficit hyperactivity disorder is a common neurobehavioral developmental disorder that usually occurs in childhood and can continue into adulthood. Researchers have discovered a number of genes linked to an increased susceptibility to ADHD. Type 2 is linked to a defect on chromosome 17p11.
  • Attention Deficit-Hyperactivity Disorder, Susceptibility to, 3: ADHD or attention deficit hyperactivity disorder is a common neurobehavioral developmental disorder that usually occurs in childhood and can continue into adulthood. Researchers have discovered a number of genes linked to an increased susceptibility to ADHD. Type 3 is linked to a defect on chromosome 6q12.
  • Attention Deficit-Hyperactivity Disorder, Susceptibility to, 4: ADHD or attention deficit hyperactivity disorder is a common neurobehavioral developmental disorder that usually occurs in childhood and can continue into adulthood. Researchers have discovered a number of genes linked to an increased susceptibility to ADHD. Type 4 is linked to a defect on chromosome 5p13.
  • Attention Deficit-Hyperactivity Disorder, Susceptibility to, 5: ADHD or attention deficit hyperactivity disorder is a common neurobehavioral developmental disorder that usually occurs in childhood and can continue into adulthood. Researchers have discovered a number of genes linked to an increased susceptibility to ADHD. Type 5 is linked to a defect on chromosome 2q21.1.
  • Attention Deficit-Hyperactivity Disorder, Susceptibility to, 6: ADHD or attention deficit hyperactivity disorder is a common neurobehavioral developmental disorder that usually occurs in childhood and can continue into adulthood. Researchers have discovered a number of genes linked to an increased susceptibility to ADHD. Type 6 is linked to a defect on chromosome 13q12.11.
  • Attention Deficit-Hyperactivity Disorder, Susceptibility to, 7: ADHD or attention deficit hyperactivity disorder is a common neurobehavioral developmental disorder that usually occurs in childhood and can continue into adulthood. Researchers have discovered a number of genes linked to an increased susceptibility to ADHD. Type 7 is linked to a defect on chromosome 12q21.
  • Australian Sea Lion poisoning: The Australian Sea Lion is sometimes used as a food source and is found in the South-Southwest waters of Australia. Eating the liver of the Australian Sea Lion can result in a Vitamin A overdose which can cause serious symptoms and even death in extreme cases.
  • Australian Umbrella Tree poisoning: The Australian Umbrella tree is an evergreen shrub or tree which originated in Asia. The sap of the plant contains oxalate which can cause irritation symptoms. Skin contact with the sap from the plant can result in irritation and eating parts of the plant can cause symptoms. The plant is considered to have low toxicity if eaten and skin irritation tends to be minor.
  • Autistic conditions: Medical conditions related to autism or autism spectrum disorders.
  • Autoimmune Diseases of the Nervous System: A group of diseases where the body's immune system attacks it's own nervous system. Examples includes opsoclonus myoclonus syndrome, Guillain-Barre syndrome and multiple sclerosis. Symptoms vary depending on which nerves are involved.
  • Autoimmune Hemolytic Anemia: Autoimmune hemolytic anemia is characterized by an abnormal immune system response which leads to the destruction of red blood cells and hence anemia. The severity of the condition varies depending on the underlying cause e.g. cytomegalovirus, hepatitis, HIV and lupus. The condition may develop gradually or occur suddenly and cause serious symptoms.
  • Autoimmune inner ear disease: A rare disorder where the body's own immune system attacks the inner ear.
  • Azarcon-induced lead poisoning: Azarcon is a lead-containing tetraoxide salt used mainly by Mexican people to treat digestive or stomach problems including indigestion and diarrhea. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
  • BANF acoustic neurinoma: A type of tumor that affects hearing and is associated with a condition called BANF (bilateral acoustic neurofibromatosis). The tumor is benign an occurs in the cells that form the myelin sheath of the vestibulocochlear nerve. The symptoms vary depending on the size and exact location of the nerve. The tumor may become large enough to compress against various cranial nerves or even the brainstem.
  • Ba Bow Sen-induced lead poisoning: Ba Bow Sen is a folk remedy used mainly by Chinese people to treat childhood hyperactivity and to alleviate nightmares. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
  • Bacterial toxic-shock syndrome: A very rare, potentially fatal infection caused by toxins produced by bacteria, especially bacteria such as Staphylococcus aureus or Streptococcus pyogenes. The condition is often associated with tampon use but can originate from other sources.
  • Balance symptoms: Problems with balance or vertigo
  • Bali goli-induced lead poisoning: Bali goli (flat black bean) is a folk remedy used mainly by Indian and Asian people to treat intestinal problems. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
  • Balint's syndrome: A condition involving a variety of visual symptoms such as optic ataxia, agnosia and nystagmus.
  • Baltic myoclonic epilepsy: A rare inherited type of progressive myoclonus epilepsy which tends to cause symptoms during childhood. The involuntary muscle movements tend to occur more frequently and become more severe with increasing age. Symptoms may occur following various stimuli such as light, stress or exercise.
  • Baneberry poisoning: Baneberries are toxic and can cause a skin reaction on contact or various poisoning symptoms.
  • Bangstad syndrome: A rare disorder characterized by diabetes, goiter, insufficient hormone production by the gonads and progressive ataxia.
  • Barbiturate abuse: Abuse of barbiturate medications
  • Barotitis Media: Middle ear inflammation or bleeding caused by differences between the middle ear air pressure and atmospheric air pressure. Can be caused by such things as scuba diving and symptoms include pain, tinnitus, diminished hearing and vertigo. Also called aerotitis media.
  • Barre-Lieou syndrome: A rare condition where trauma (such as pinching by adjacent vertebrae or arthritis) to the sympathetic nerves located in the spinal area of the neck results in a variety of neurological symptoms.
  • Bartschi-Rochaix syndrome: A range of symptoms caused by compression of the cerebral artery.
  • Basal Ganglia Disease, Adult-Onset: A rare disorder where a genetic mutation results in a neurological disease resulting from abnormal iron and ferritin deposits in the brain.
  • Basal ganglia calcification, idiopathic 1: Abnormal calcium deposits in the part of the brain called the basal ganglia. Type 1 results in psychiatric, cognitive or neurological problems associated with the calcification. The symptoms experienced are variable.
  • Basilar artery insufficiency: refers to a temporary set of symptoms due to decreased blood flow in the posterior circulation of the brain
  • Basilar artery insufficiency syndrome: A range of symptoms caused by impaired blood flow through the basilar artery. The symptoms may come and go according to variation in blood flow through the basilar artery. The blood flow may be impaired by such things as thrombosis, narrowed artery and blood vessel spasms. Symptoms vary depending on the exact location and extent of the artery involvement as well as whether the onset is gradual or sudden.
  • Basilar artery migraine: Basilar migraine (BM), also known as Bickerstaff syndrome, consists of headache accompanied by dizziness, ataxia, tinnitus, decreased hearing, nausea and vomiting, dysarthria, diplopia, loss of balance, bilateral paresthesias or paresis, altered consciousness, syncope, and sometimes loss of consciousness.
  • Basilar impression primary: A congenital bone abnormality where the skull and vertebrae meet which can compress some of the brain structures and result in neurological abnormalities. The defect is often associated with other vertebral abnormalities. In severe cases, the cerebrospinal fluid flow may be obstructed which can cause fluid to build up inside the skull (hydrocephalus).
  • Basilar migraine: Basilar migraine is a type of headache accompanied by neurological symptoms such as vision problems, coordination problems and vertigo.
  • Batten Disease: Rare childhood genetic degenerative nerve system disease.
  • Batten-Turner muscular dystrophy: A benign form of congenital muscular dystrophy involving relatively minor muscle wasting. The condition progresses slowly until adulthood.
  • Baughman syndrome: A rare syndrome characterized mainly by fused eyelids, curly hair and abnormal nails.
  • Beer-drinker syndrome: Symptoms that can occur when large amounts of beer is consumed with little or no food.
  • Behcet's syndrome: Recurring inflammation of small blood vessels affecting various areas.
  • Behr syndrome: A rare inherited neurological condition characterized by spastic paraplegia and sometimes optic atrophy.
  • Benign Fasciculation Syndrome: Common movement disorder manifesting in a fine (fast) tremor; it is an inherited condition of unknown cause.
  • Benign Paroxysmal Positional Vertigo: A condition where certain head movements cause extreme dizziness.
  • Benign paroxysmal torticollis of infancy: A harmless condition characterized by recurring periods of head tilting resulting from dystonia (sustained muscle contractions) of the neck muscles. Other symptoms such as vomiting and irritability may also occur variably. Episodes tend to occur without any noticeable triggers and may last from hours to days. Episodes can occur as often as every two weeks or as infrequently as every couple of months.
  • Bernheim syndrome: Overgrowth of the left heart ventricle which results in the tissue separating the two ventricles pushing into the right ventricle. This results in obstruction of blood flow through the right heart ventricle and ultimately can lead to heart failure.
  • Bhaskar-Jagannathan syndrome: A very rare syndrome characterized primarily by long, thin fingers, amino acids in the urine, cataracts (during infancy), incoordination and delayed development.
  • Bickerstaff's brainstem encephalitis: A rare condition where inflammation of the brainstem results in various symptoms such as ataxia and ophthalmoplegia. The onset of symptoms is usually acute.
  • Bickerstaff's brainstem encephalitis (BBE): A rare condition where inflammation of the brainstem results in various symptoms such as ataxia and ophthalmoplegia. The onset of symptoms is usually acute.
  • Biemond Syndrome: A rare genetic disorder characterized by nystagmus, cerebellar ataxia and short digits.
  • Biemond syndrome type 1: A rare inherited condition characterized by mental retardation, finger and toe abnormalities, obesity and eye problems.
  • Bilateral cerebellar ataxia: gross incoordination of muscle movement
  • Binswanger Disease: Multi-infarct dementia, caused by damage to deep white matter.
  • Binswanger's Disease: A type of senile dementia characterized by chronic cerebrovascular disease.
  • Bint Al Zahab-induced lead poisoning: Bint Al Zahab is a folk remedy used by various ethnic groups (e.g. Indians, Saudi Arabians) to treat infant colic and to facilitate the passage of meconium in newborns. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
  • Biotinidase deficiency: A metabolic disorder where the body lacks the enzyme biotinidase needed to process the vitamin called biotin (vitamin H) into carboxylase enzymes.
  • Biotinidase deficiency, late onset: A metabolic disorder where the body lacks the enzyme biotinidase needed to process the vitamin called biotin (vitamin H) into carboxylase enzymes. The severity of symptoms may vary depending on the degree of deficiency. Severe cases can result in metabolic acidosis which can lead to death if treatment isn't given.
  • Bird of Paradise poisoning: Various parts of the Bird of Paradise plant are poisonous - the seeds contain toxic tannins and the leaves can contain hydrocyanic acid. Eating five seed pods can result in poisoning symptoms but the plant is generally considered to have low toxicity.
  • Bird-headed dwarfism with progressive ataxia, Insulin-resistant diabetes, goiter and primary gonadal insufficiency: A rare disorder characterized by diabetes, goiter, insufficient hormone production by the gonads and progressive ataxia.
  • Black nightshade poisoning: The Black Nightshade is a herb which bears small white or purple flowers and dull black berries. The plant originated in South America. The berries contain solanine alkaloid which can be toxic if eaten in large quantities. The leaves and unripe berries are considered toxic whereas the ripe fruit is possibly edible.
  • Bleeding Heart poisoning: Bleeding heart is a vine plant that can cause skin reactions on exposure and systemic symptoms such as convulsions if eaten. The leaves and roots are the most toxic parts of the plant and contain a toxic chemical called isoquinoline. Large amounts of the plant need to be eaten for poisoning to occur. The plant is native to North America.
  • Bleeding symptoms: Any type of bleeding symptoms.
  • Bloodroot poisoning: The Bloodroot is a flowering herb that bears fruit and whose stem contains red juices. The plant tends to grow in mountainous areas. The thickened roots (rhizomes) of the plant contain isoquinoline alkaloids which are very toxic and can cause death if eaten in sufficient quantities.
  • Blue-ringed octopus poisoning: The blue-ringed octopus is found in shallow Australian ocean water and can deliver venomous, potentially fatal bite. The poison is present in the saliva of the octopus. The venom affects the neuromuscular system.
  • Bog rosemary poisoning: Bog rosemary is a type of heath found in bogs and cold peat areas of the more northern parts of the world. It is a small shrub with tall thin stems. The flowers are whit or pink. The plant contains a chemical called grayanotoxin which can cause various symptoms if eaten. The plant is only considered poisonous if large amounts are eaten.
  • Bokhoor-induced lead poisoning: Bokhoor is a traditional used mainly by Saudi Arabian people to calm infants - it involves burning wood and lead sulphide and inhaling the fumes that are produced. This practice has the potential to cause lead poisoning due to the relatively high exposure to lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
  • Bonefish poisoning (clupeotoxin): Some bonefish contain toxins (Clupeotoxin) which can be poisonous to humans if eaten. Heat does not destroy the toxin and there is still uncertainty as to the origin of the toxin. The toxin appears to be present in higher concentrations in summer and is believed to be possible linked to the consumption of toxic food in its food web. The size and age of the bonefish does not appear to be related to the toxicity. The bonefish are found in coastal waters off Africa and the Caribbean, Indian and Pacific Oceans.
  • Bonneman-Meinecke-Reich syndrome: A very rare syndrome characterized by calcium deposits in the brain tissue, deficiency of growth hormones and degeneration of the part of the eye called the retina.
  • Bonnemann-Meinecke-Reich syndrome: A rare disorder characterized mainly by growth problems, vision problems and brain disease.
  • Bonnier's syndrome: A range of symptoms caused by damage to Dieter's nucleus (the lateral nucleus of the vestibular nerve) or its connections.
  • Borud Syndrome: A very rare syndrome characterized by numerous features including hearing and vision problems, heart muscle disease, ataxia and peripheral neuropathy.
  • Botulism food poisoning: Extremely dangerous food poisoning requiring medical attention, but not always recognized because of its non-abdominal symptoms.
  • Boxwood poisoning: The boxwood is an evergreen, woody, flowering shrub often used as a hedge. The leaves contain steroidal alkaloids which can cause skin irritation upon skin contact with the sap or various other symptoms if eaten. The plant is considered to have a relatively low level of toxicity.
  • Brachydactyly nystagmus cerebellar ataxia: A very rare syndrome characterized mainly by short digits, nystagmus and cerebellar ataxia.
  • Bracken fern poisoning: Bracken fern is a type of fern which contains chemicals (glycoside and thiaminase) and can cause symptoms if eaten. The plant is considered to have a relatively low level of toxicity. The new leaf growths (fiddleheads) are actually safely edible.
  • Bradbury-Eggleston syndrome: A syndrome mainly involving reduced blood pressure, lightheadedness or fainting on standing, dizziness and visual disturbances that is associated with a degeneration of the autonomic nerve system. It is most common in older males. Symptoms tend to be worse in the morning, after eating, after exercise or in hot weather.
  • Brain Concussion: Trauma resulting in minor injury to the brain which causes a period of interrupted brain function. Simple concussions resolve themselves in about a week whereas more serious ones have persisting symptoms. The onset of symptoms may be delayed.
  • Brain Stem Neoplasms: A brain stem tumor. The tumor may be malignant or benign and the severity of the condition is determined by the size of the tumor and exact location.
  • Brain symptoms: Symptoms affecting the brain
  • Brain tumor, adult: A growth or tumor that develops in the tissues of the brain in adults. The tumor can be benign or malignant.
  • Brainstem glioma: tumour of the brain
  • Breynia officinalis poisoning: Ingestion of the Breynia officinalis plant can cause irritation to mucosal linings and liver problems. The plant is often used as a herbal drug (Chi R Yun) to treat such things as poor growth, heart failure and venereal disease.
  • Brief Psychotic Disorder: Episodes of brief psychosis
  • Broad bean poisoning: The broad bean is a vine which produces pea-like flowers and long, seed-filled pods. The seeds can be very toxic and can result in death if eaten. This toxic reaction only occurs to certain susceptible people who are unable to process certain chemicals in the plant. The resulting condition is called favism and is most common in people of Mediterranean descent.
  • Bronchopulmonary dysplasia: A condition which is characterized by dysplasia of the brochopulmonary vessels
  • Brown-Vialetto-Van Laere syndrome: A very rare progressive disorder characterized by nerve deafness and cranial (and sometimes spinal) nerve paralysis.
  • Brun's syndrome: Various neurological symptoms caused by an obstruction of the flow of cerebrospinal fluid with certain head postures. The obstruction is often due to some sort of brain tumor or cyst. Symptoms come and go depending on the position of the head.
  • Buckeye poisoning: Buckeye is a shrub or small tree which contains a toxic compound called aesculin that can cause gastrointestinal or neuromuscular symptoms. Young leaves, flowers and bark are the most toxic parts of the plant. The plant is most common in parts of North America. Eating only one or two seeds may simply cause vomiting or diarrhea but repeated exposure or eating large amounts can cause more serious symptoms.
  • Buffalo pea poisoning: The buffalo pea is a poisonous plant which contains a toxic compound called quinolizidine alkaloid. The plant is mainly found in Western Canada.
  • Bushmaster poisoning: The Bushmaster is a poisonous snake found in America.
  • Bárány syndrome: A rare syndrome characterized by various symptoms associated with a headache that occurs on one side of the back of the head.
  • CACH syndrome: A rare syndrome characterized mainly by childhood ataxia and reduced myelination of the cerebral nerves. Motor and mental development in the first few years of life is normal with progressive neurodegeneration occurring between 2 and 5 years of age. Fever and trauma to the head can speed up disease progression.
  • CANOMAD syndrome: A rare syndrome characterized by a range of abnormalities caused by immune-mediated nerve demyelination. There is usually no loss of limb function associated with the disorder. The face, throat, mouth and eye symptoms (weakness of the muscles) usually come and go.
  • CDG syndrome type 1A: A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1A involves a phosphomannomutase enzyme defect and affects most body systems especially the nervous system and liver function.
  • CDG syndrome type I: A rare genetic disorder where the body is unable to synthesize glycoproteins which results in multisystem problems.
  • CDG syndrome type Ic: A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1C has a differs from the other subtypes by the type of enzyme which is deficient.
  • CFS subtype 1 (cognitive, musculoskeletal, sleep, anxiety/depression): Chronic fatigue syndrome is a chronic condition which is characterized by symptoms such as severe persistent fatigue, depression, weakness, muscle pain and lack of energy. The condition is often debilitating and may be difficult to diagnose due to lack of specific tests for the condition. There is no known cause but it appears to be associated with a previous infection in some cases. CFS subtype 1 tends to be more severe with the dominant symptoms being anxiety, depression and cognitive, musculoskeletal and sleeping problems.
  • CFS subtype 2 ( musculoskeletal, pain, anxiety/depression): Chronic fatigue syndrome is a chronic condition which is characterized by symptoms such as severe persistent fatigue, depression, weakness, muscle pain and lack of energy. The condition is often debilitating and may be difficult to diagnose due to lack of specific tests for the condition. There is no known cause but it appears to be associated with a previous infection in some cases. CFS subtype 2 tends to be more severe with the dominant symptoms being anxiety, depression, pain and musculoskeletal problems.
  • CFS subtype 3 (mild): Chronic fatigue syndrome is a chronic condition which is characterized by symptoms such as severe persistent fatigue, depression, weakness, muscle pain and lack of energy. The condition is often debilitating and may be difficult to diagnose due to lack of specific tests for the condition. There is no known cause but it appears to be associated with a previous infection in some cases. CFS subtype 3 tends to have milder symptoms than other subtypes.
  • CFS subtype 4 (cognitive, musculoskeletal, sleep, anxiety/depression): Chronic fatigue syndrome is a chronic condition which is characterized by symptoms such as severe persistent fatigue, depression, weakness, muscle pain and lack of energy. The condition is often debilitating and may be difficult to diagnose due to lack of specific tests for the condition. There is no known cause but it appears to be associated with a previous infection in some cases. CFS subtype 4 tends to be dominated by cognitive symptoms.
  • CFS subtype 5 (musculoskeletal, gastrointestinal): Chronic fatigue syndrome is a chronic condition which is characterized by symptoms such as severe persistent fatigue, depression, weakness, muscle pain and lack of energy. The condition is often debilitating and may be difficult to diagnose due to lack of specific tests for the condition. There is no known cause but it appears to be associated with a previous infection in some cases. CFS subtype 5 tends to be dominated by musculoskeletal and gastrointestinal symptoms.
  • CFS subtype 6 (postexertional): Chronic fatigue syndrome is a chronic condition which is characterized by symptoms such as severe persistent fatigue, depression, weakness, muscle pain and lack of energy. The condition is often debilitating and may be difficult to diagnose due to lack of specific tests for the condition. There is no known cause but it appears to be associated with a previous infection in some cases. CFS subtype 6 tends to be dominated by excessive fatigue following exertion.
  • CFS subtype 7 (pain, infectious, musculoskeletal, sleep, neurological, gastrointestinal, neurocognitive, anxiety/depression): Chronic fatigue syndrome is a chronic condition which is characterized by symptoms such as severe persistent fatigue, depression, weakness, muscle pain and lack of energy. The condition is often debilitating and may be difficult to diagnose due to lack of specific tests for the condition. There is no known cause but it appears to be associated with a previous infection in some cases. CFS subtype 7 tends to be more severe with the dominant symptoms being pain, infections, anxiety, depression and musculoskeletal, sleep, neurological, gastrointestinal and neurocognitive problems.
  • COACH syndrome: A very rare syndrome characterized by ataxia, gaps or holes in various eye structures, mental retardation, liver fibrosis and brain abnormalities.
  • California encephalitis: An uncommon mosquito born virus (California encephalitis virus) which can cause brain inflammation in humans. The severity of symptoms is variable. The incubation period can last from a few days to a week. Infants and children tend to be more severely affected than adults who sometimes have no obvious symptoms.
  • Carbamoyl-phosphate synthase 1 deficiency: A very rare inherited urea cycle disorder where the lack of the enzyme carbamoyl phosphate synthetase prevents ammonia from being turned into urea and being excreted in the urine. Excess ammonia builds up in the body which can cause serious complications or even death if left untreated.
  • Cardiac tamponade: Symptoms caused by compression of the heart due to the accumulation of blood or fluid in the space between the heart muscle and the membrane covering the heart.
  • Catamenial seizure: A type of seizure that is associated with the female menstrual cycle. It appears that flucutations in hormone levels leads to increased seizure activity in some women just before or during their menstrual cycle. Simple or complex partial seizures or generalized tonic-clonic seizures may be involved.
  • Cataract -- ataxia -- deafness: A rare syndrome characterized by cataracts, ataxia and progressive deafness.
  • Cebagin-induced lead poisoning: Cebagin is a folk remedy used mainly by Middle Eastern people to treat teething. This folk remedy has the potential to cause lead poisoning due to its relatively high content of lead. Children are more susceptible to the effects of lead. The use of folk remedies is still prevalent in some cultures. Lead poisoning can result in serious illness and even death in severe cases.
  • Celiac disease, susceptibility to 1: The susceptibility to developing celiac disease due to a genetic defect on chromosome 6p21.3. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 10: The susceptibility to developing celiac disease due to a genetic defect on chromosome 3q25-q26. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 11: The susceptibility to developing celiac disease due to a genetic defect on chromosome 3q28. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 12: The susceptibility to developing celiac disease due to a genetic defect on chromosome 6q25.3. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 13: The susceptibility to developing celiac disease due to a genetic defect in the SH2B3 gene on chromosome 12q24. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 2: The susceptibility to developing celiac disease due to a genetic defect on chromosome 5q31-q33. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 3: The susceptibility to developing celiac disease due to a genetic defect on chromosome 2q33. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 4: The susceptibility to developing celiac disease due to a genetic defect on chromosome 19p13.1. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 5: The susceptibility to developing celiac disease due to a genetic defect on chromosome 15q11-q13. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 6: The susceptibility to developing celiac disease due to a genetic defect on chromosome 4q27. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 7: The susceptibility to developing celiac disease due to a genetic defect on chromosome 1q31. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 8: The susceptibility to developing celiac disease due to a genetic defect on chromosome 2q11-q12. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 9: The susceptibility to developing celiac disease due to a genetic defect on chromosome 3p21. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Central nervous system lymphoma, primary: A type of lymphoma that occurs in the central nervous system (brain and spinal cord). A lymphoma consists of cancerous lymphocytes which are a type of white blood cell. Symptoms vary according to the location of the lymphoma.
  • Central nervous system oxygen toxicity: High oxygen levels which affects the central nervous system. The condition can occur during deep dives with fatal consequences.
  • Central nervous system protozoal infections: A protozoal infection of the central nervous system (spinal cord or brain). The infection may originate in the central nervous system (primary infection) or may spread from another part of the body (secondary infection). The infection may occur in otherwise healthy individuals or in individuals who have a compromised immune system. Primary protozoal CNS infections include cerebral amebiasis, granulomatous amebic encephalitis and secondary infections include cerebral malaria and cerebral babesiosis.
  • Central pontine myelinolysis: A rare condition where the protective layer around brainstem nerve cells is destroyed which prevents nerve signals being transmitted properly. It generally occurs in response to a rapid change in sodium levels in the body which can be caused by treatment of various conditions or by various conditions that cause rapid sodium level changes.
  • Cephalosporin-induced Immune Hemolytic Anemia: Cephalosporin-induced immune hemolytic anemia is a condition where a use of a medication called Cephalosporin triggers the body's immune system to destroy it's own red blood cells which results in anemia.
  • Cerebellar Ataxia, Deafness and Narcolepsy: A rare condition characterized by the association of narcolepsy, deafness and cerebellar ataxia. Narcolepsy is a sleep disorder where characterized by the classic tetrad of excessive daytime sleepiness, cataplexy, hypnagogic hallucinations and sleep paralysis.
  • Cerebellar ataxia: Cerebellar ataxia is a form of ataxia originating in the cerebellum. Romberg's test can be used to distinguish cerebellar ataxia from other forms of ataxia
  • Cerebellar ataxia -- areflexia -- pes cavus -- optic atrophy -- sensorineural hearing loss: A rare syndrome characterized mainly by ataxia, absent reflexes, high foot arch (pes cavus), progressive optic nerve degeneration and hearing impairment. The ataxic symptoms tended to occur early in life after an illness involving fevers. The ataxia then tends to come and go but then persists into adulthood. The severity of symptoms is variable.
  • Cerebellar ataxia -- ectodermal dysplasia: A rare syndrome characterized by balance and coordination problems and teeth and hair abnormalities.
  • Cerebellar ataxia -- intellectual deficit -- optic atrophy -- skin abnormalities: A rare syndrome characterized by ataxia, mental retardation, optic atrophy and skin abnormalities.
  • Cerebellar ataxia in children: Cerebellar ataxia in children refers to a child who has uncoordinated muscle movements.
  • Cerebellar ataxia type 1, autosomal recessive: A slow progressing brain disorder characterized by ataxia and dysarthria.
  • Cerebellar ataxia, X-linked: A disorder where degeneration of certain parts of the brain results in symptoms such as ataxia. The rate of progression can vary.
  • Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss: A rare syndrome characterized mainly by ataxia, absent reflexes, high foot arch (pes cavus), progressive optic nerve degeneration and hearing impairment. The ataxic symptoms tended to occur early in life after an illness involving fevers. The ataxia then tends to come and go but then persists into adulthood.
  • Cerebellar ataxia, autosomal recessive: A group of rare, recessively inherited neurological disorders caused by abnormalities in the cerebellum and spinal cord. In some cases other parts of the body may be affected.
  • Cerebellar ataxia, dominant pure: A dominantly inherited form of ataxia that involves only the cerebellar system.
  • Cerebellar ataxia, infantile with progressive external ophthalmoplegia: A rare disorder characterized by cerebellar ataxia during infancy and progressive paralysis of eye muscles.
  • Cerebellar degeneration, subacute: A rare disorder involving degeneration of the cerebellum and sometimes involves nearby spinal cord or brain tissue.
  • Cerebellar hypoplasia -- endosteal sclerosis: A rare disorder character where a part of the brain (cerebellum) is underdeveloped and abnormally increased bone density (endosteal sclerosis).
  • Cerebellar hypoplasia -- tapetoretinal degeneration: A rare disorder character where a part of the brain (cerebellum) is underdeveloped and a nonprogressive eye disorder involving the retinal pigments. The cerebellum is the part of the brain that controls balance and movement.
  • Cerebelloolivary atrophy: The degeneration of the parts of the brain called the cerebellum and the olives. Symptoms may vary from case to case depending on the severity and extent of the degeneration.
  • Cerebelloparenchymal autosomal recessive disorder 3: A rare, recessively inherited disorder characterized mainly by albinism, incoordination, low muscle tone and eye problems.
  • Cerebelloparenchymal disorder V: An inherited brain disorder characterized by myoclonic jerks which become more apparent during voluntary movements.
  • Cerebellum agenesis -- hydrocephaly: A rare brain disorder which manifests as reduced muscle tone, ataxia, cataracts and mental retardation.
  • Cerebral Amyloid Angiopathy, Familial: A rare disorder where abnormal deposits of amyloid in the brain blood vessels causes spasticity, incoordination and dementia. Brain hemorrhage and strokes may also result in severe cases.
  • Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy: A rare inherited condition characterized primarily by progressive degeneration of the brain white matter and disease of the brain blood vessels as well as additional symptoms not involving the brain e.g. thin skin, alopecia and spinal disc disease.
  • Cerebral Palsy: Any brain disorder causing movement disability
  • Cerebral Palsy, Ataxic, Autosomal Recessive: Ataxic cerebral palsy refers to an injury to the brain that results primarily in low muscle tone and poor coordination of movements. The ataxic autosomal recessive form is an inherited abnormality in the development of the brain which is linked to chromosome 9p12-q12
  • Cerebral astrocytoma, adult: A very rare tumor that occurs in adults and develops in brain cells called astrocytes. The part of the brain involved is the cerebrum at the top of the head which controls functions such as reading, writing, thinking, learning, speech, emotion and voluntary movement.
  • Cerebral contusion: Injury of the cerebrum often causing bruising when the skin is not broken.
  • Cerebral gigantism -- jaw cysts: A very rare syndrome characterized mainly by abnormal brain development and jaw cysts.
  • Cerebral sarcoma: A type of brain tumor that can be inherited in an autosomal dominant manner. The tumor arises from blood vessels in the brain. Symptoms may vary depending on the size and exact location of the tumor.
  • Cerebrorenodigital syndrome: A rare group of syndromes characterized mainly by brain, kidney, finger and toe abnormalities.
  • Cerebrotendinous Xanthomatosus: A rare syndrome where a genetic mutation results in a metabolic disorders caused by a deficiency of sterol 27-hydroxylase deficiency. The condition causes progressive neurological dysfunction, cataracts and premature atherosclerosis. Deposits of cholesterol and cholestanol can be found in any part of the body including the brain. The rate of progression and severity of symptoms varying amongst patients. The degree of neurological involvement is also variable.
  • Cerebrovascular Conditions: Conditions of the brain's blood vessels including stroke.
  • Ceroid lipofuscinosis, neuronal 1, infantile: A rare inherited biochemical disorder involving the progressive accumulation of certain chemicals (lipopigments) in body tissues due to deficiency of an enzyme (palmitoyl-protein thioesterase) needed to process it.
  • Ceroid lipofuscinosis, neuronal 10: A rare metabolic disorder that affects the nerve cells of the body and is characterized by the deposits of lipopigments (lipofuscin). Type 10 involves a deficiency of cathepsin D and involves an initial period of normal development with neurodegenerative symptoms starting during the early school years.
  • Ceroid lipofuscinosis, neuronal 2, late infantile type: A rare inherited biochemical disorder involving the progressive accumulation of certain chemicals (lipopigments) in body tissues due to deficiency of an enzyme (protease tri-peptidyl-peptidase) needed to process it.
  • Ceroid lipofuscinosis, neuronal 3, Juvenile: A progressive genetic disorder where defective lipid metabolism that causes blindness, neurological deterioration, dementia leading to total incapication within years and death within 10-15 years.
  • Ceroid lipofuscinosis, neuronal 4: A rare inherited biochemical disorder involving the progressive accumulation of certain chemicals (lipopigments) in body tissues due to deficiency of an enzyme (palmitoyl-protein thioesterase 1) needed to process it.
  • Ceroid lipofuscinosis, neuronal 7: A rare metabolic disorder that affects the nerve cells of the body and is characterized by the deposits of lipopigments (lipofuscin). Type 7 is distinguished from other types by the origin of the genetic defect.
  • Ceroid lipofuscinosis, neuronal 8: A rare metabolic disorder that affects the nerve cells of the body and is characterized by the deposits of lipopigments (lipofuscin). Type 8 is distinguished from other types by the origin of the genetic defect.
  • Charcot-Marie-Tooth Disorder: Degeneration of limb muscles.
  • Charcot-Marie-Tooth disease (generic term): A group of inherited neurological disorders characterized by problems with the peripheral nerves. Muscle weakness, muscle wasting and sensory problems are the most common symptoms. The severity and age of onset of symptoms varies depending on the specific subtype of the disorder.
  • Charcot-Marie-Tooth disease -- deafness: Charcot-Marie-Tooth disease is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Charcot-Marie-Tooth disease and deafness involves the usual CMT symptoms as well as deafness.
  • Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 5 has an autosomal dominant inheritance, progresses slowly and involves movement disorders.
  • Charcot-Marie-Tooth disease, Type 1A: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 1A is inherited as an autosomal dominant pattern and involves the duplication of the PMP22 gene on chromosome 17.
  • Charcot-Marie-Tooth disease, Type 1B: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 1B is inherited as an autosomal dominant pattern and involves a defect in the MPZ gene on chromosome 1. The severity of the condition is variable depending on the age of onset with severe infantile cases resulting in the inability to walk at an early age.
  • Charcot-Marie-Tooth disease, Type 1C: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 1C is inherited as an autosomal dominant pattern and involves a defect in the LITAF/SIMPLE gene on chromosome 16.
  • Charcot-Marie-Tooth disease, Type 1D: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 1D is caused by a defect of the ERG2 gene on chromosome 10 and usually results in a severe form of the disease.
  • Charcot-Marie-Tooth disease, Type 1E: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 1E involves the usual CMT symptoms as well as deafness.
  • Charcot-Marie-Tooth disease, Type 1F: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 1F is caused by a defect of a gene in chromosome 8 and involves the neurofilament light chain protein.
  • Charcot-Marie-Tooth disease, Type 2A: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function.
  • Charcot-Marie-Tooth disease, Type 2AI: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 2A1 has an autosomal dominant inheritance and involves a defect in the KIF1B gene on chromosome 1p36.
  • Charcot-Marie-Tooth disease, Type 2AII: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 2A2 has an autosomal dominant inheritance and involves a defect in the MFN2 gene on chromosome 1p36.
  • Charcot-Marie-Tooth disease, Type 2C: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 2C has an autosomal dominant inheritance and involves a defect in chromosome 12 and involves diaphragm and vocal cord weakness as well as hand and foot problems.
  • Charcot-Marie-Tooth disease, Type 2D: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 2D has an autosomal dominant inheritance and involves a defect in the glycyl RNA synthetase gene on chromosome 7p15. The hands tend to be more severely affected than the feet.
  • Charcot-Marie-Tooth disease, Type 2E: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 2C has an autosomal dominant inheritance and involves a defect in the neurofilament light gene on chromosome 8p21.
  • Charcot-Marie-Tooth disease, Type 4A: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 4A has an autosomal recessive inheritance and involves a defect in the GDAP 1 protein gene on chromosome 8. The recessive forms of CMT tend to be more severe than the dominant form and often involve hand and foot problems as well as additional systemic symptoms.
  • Charcot-Marie-Tooth disease, Type 4B1: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 4B1 has an autosomal recessive inheritance and involves a defect in MTMR2 gene on chromosome 11.
  • Charcot-Marie-Tooth disease, Type 4C: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 4B2 has an autosomal recessive inheritance and involves a defect in the KIAA1985 gene on chromosome 5. It involves motor and sensory problems as well as scoliosis.
  • Charcot-Marie-Tooth disease, Type 4E: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 4B2 has an autosomal recessive inheritance and involves a defect in the EGR2 gene on chromosome 10.
  • Charcot-Marie-Tooth disease, Type 4F: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 4F has an autosomal recessive form of inheritance and is a severe form of the disease. It involves a defect in the PRX gene on Chromosome 19q13.
  • Charcot-Marie-Tooth disease, Type 4G: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 4G has an autosomal recessive form of inheritance and is a severe form of the disease. It involves a defect on Chromosome 10.
  • Charcot-Marie-Tooth disease, X-linked, 1: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type X1 is an inherited defect of the X chromosome (defect in GJB1 gene) and affects males to a greater degree than females. Transient central nervous system symptoms are also sometimes involved.
  • Charcot-Marie-Tooth disease, type 4: A rare group of demyelinating motor and sensory neuropathies consisting of a number of subtypes. The various subtypes are caused by different genetic defects.
  • Charcot-Marie-Tooth, demyelinating, autosomal recessive: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 4 has an autosomal recessive form of inheritance and is a severe form of the disease.
  • Chediak-Higashi Syndrome: An inherited immune system disorder resulting in frequent infections, lack of skin and eye pigmentation, neurological diseases and early death.
  • Chediak-Higashi like syndrome: A rare genetic disorder characterized mainly by albinism (lack of pigmentation). There are three different subtypes of the disorder (I, II and III) each with varying additional features such as immunodeficiency and neurological symptoms. Type 1 involves partial albinism and neurological symptoms, type II involves partial albinism, immunodeficiency and sometimes neurological symptoms and type III involves albinism only.
  • Chemical burn -- airways: Burns to the airways caused by a chemical - usually through inhalation but can also occur through aspiration if the chemical is swallowed. Symptoms vary depending on the type, quantity and strength of the chemical involved as well as the duration of the exposure to the chemical and promptness of treatment measures. Immediate medical attention should be sought if chemical burns to the airways are suspected.
  • Chemical burn -- ingestion: Burns to the mouth and gastrointestinal system caused by swallowing a chemical. Symptoms vary depending on the type, quantity and strength of the chemical involved as well as the duration of the exposure to the chemical and promptness of treatment measures. Immediate medical attention should be sought if chemical burns to the gastrointestinal system are suspected.
  • Chemical burn -- inhalation: Burns to the airways caused by a chemical through inhalation. Symptoms vary depending on the type, quantity and strength of the chemical involved as well as the duration of the exposure to the chemical and promptness of treatment measures. Immediate medical attention should be sought if chemical burns to the airways are suspected.
  • Chemical burn -- skin: Burns to the skin caused by a chemical. Symptoms vary depending on the type, quantity and strength of the chemical involved as well as the duration of the exposure to the chemical and promptness of treatment measures.
  • Chemical burns: burns causing protein coagulation
  • Chemical pneumonia: Lung inflammation from inhaled chemicals
  • Chemical poisoning: Morbid condition caused by chemical.
  • Chemical poisoning -- 1,1-Dichloroethene: 1,1-Dichloroethene is a chemical used in packaging, food wraps, carpet backing, adhesives and steel pipe coating. The main effects of an overdose of this chemical central nervous depression and central nervous system depression. However, some people can suffer an adverse reaction to the chemical. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- 1,2-Dibromo-3-Chloropropane: 1,2-Dibromo-3-Chloropropane is a chemical used in soil fumigants and as a nematocide for various field crops. Commercial examples include Fumagon, Nemagon, Fumazone, Nemapax, Nemafume. Excessive exposure to this chemical can cause relatively mild symptoms. The chemical may be absorbed through the skin. The severity of symptoms varies depending on the amount of chemical involved and the route of exposure.
  • Chemical poisoning -- 1,2-Dibromoethane: 1,2-Dibromoethane is a chemical used in gasoline, soil fumigants, fire extinguishers, flue gases and mechanical gauge fluid. Excessive exposure to this chemical can cause serious symptoms. Some people can suffer an adverse reaction to the chemical. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- 1,3-Butadiene: 1,3-Butadiene is a chemical used in crop fungicides, carpet backing, paper coating and foams. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- 1,3-Dichloropropene: 1,3-Dichloropropene is a chemical used in solvents and soil fumigants for nematode control. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- 1,3-Dinitrobenzene: 1,3-Dinitrobenzene is a chemical used mainly in explosives. The chemical can be readily absorbed through the skin and cause systemic symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- 1-Pentanethiol: 1-Pentanethiol is a chemical used mainly in pesticides. 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 -- 1-Propanol: 1-Propanol is a chemical used in various antiseptics, polishes, cleaners, cosmetics and lacquer. The main effects of an overdose of this chemical is depression of the central nervous system. However, some people can suffer an adverse reaction to the chemical.
  • Chemical poisoning -- 2,4,6-Trichlorophenol: 2,4,6-Trichlorophenol is a chemical used mainly as an antiseptic, pesticide, wood preservative, glue preservative and as an antimildew agent in the textile manufacturing industry. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- 2,4-Dinitrotoluene: 2,4-Dinitrotoluene is a chemical used the production of explosives, vehicle air bags and polyurethane polymers. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- 2-Aminopyridine: 2-Aminopyridine is a chemical used mainly in the production of various medicines (especially antihistamines and anti-inflammatories). 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 -- 2-Butoxyethanol: 2-Butoxyethanol is a chemical used mainly in dry cleaning, textile dyeing, protective coatings, glass cleaners, solvents, cleaning agents and paint thinners. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- 3,3-Dichlorobenzidine: 3,3-Dichlorobenzidine is a chemical used mainly in the production of pigments for various items such as paint, ink, textiles and plastics. The chemical may be absorbed through the skin. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- 4,4-Methylenebis: 4,4-Methylenebis is a chemical used in the manufacture of epoxy resins, belt drives, gun mounts, shoe laces and various other manufactured goods. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- 4-Aminodiphenyl: 4-Aminodiphenyl is a chemical used mainly in research and laboratory facilities. 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 -- 4-Aminopyridine: 4-Aminopyridine is a pesticide used mainly to control bird pests. 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 -- Acetone: Acetone is a chemical used as a solvent in products such as glues, rubber cement and fingernail polish remover. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Acetophenone: Acetophenone is a chemical used mainly as a fragrance, food flavoring agent and as a solvent for plastics and resins. It is also found naturally in small quantities in foods such as bananas, apples and beef. 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 -- Acetylene: Acetylene is a chemical used mainly as a mixing gas for welding. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Acetylene Dichloride: Acetylene Dichloride is a chemical used mainly in the production of perfumes, dyes and thermoplastics. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Acetylsalicylic Acid: Acetylsalicylic Acid is also known as aspirin and is primarily used to relieve pain, fever and inflammation. Excessive exposure 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 -- Acrinathrin: Acrinathrin is a pyrethroid chemical used as an insecticide. The chemical is toxic to the nerve system. 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 -- Acrylamide: Acrylamide is a chemical used mainly in the treatment of waste water, grout agent, paper strengthening agent and adhesive agents. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Acrylonitrile: Acrylonitrile is a chemical used mainly in the production of acrylic and modacrylic fibers but also in the production of certain plastics, nylon dyes, drugs and pesticides. 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 -- Adiponitrile: Adiponitrile is a chemical used mainly in the production of hexamethylene diamine which in turn is used mainly to produce nylon. 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 -- Aftershave: Aftershave contains chemicals (ethyl alcohol, isopropyl alcohol) which can cause symptoms if ingested in sufficient quantities. Death from ingesting aftershave is considered unlikely. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Agrocide: Agrocide is a chemical insecticide used mainly to control scabies or lice as well as other agricultural insect pests. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. 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 -- Agronexit: Agronexit is a chemical insecticide used mainly as an agricultural insecticide. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. 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 -- Alachlor: Alachlor is a herbicide. 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 -- Alanycarb: Alanycarb is a carbamate pesticide used mainly as an insecticide and nematicide. 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Aldicarb: Aldicarb is a carbamate pesticide used mainly as an insecticide, nematicide and acaricide. 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Aldoxycarb: Aldoxycarb is a carbamate pesticide used mainly as an insecticide and acaricide. 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Aldrin: Aldrin is a chemical once used mainly in insecticides for crops and as a termite preventative. The chemical can readily be absorbed through the skin. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Allethrin: Allethrin is a chemical used as an insecticide, mainly in households. 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 -- Allyl chloride: Allyl chloride is a chemical used mainly in the manufacture of epichlorohydrin and glycerin but is also used in the production of products such as polyester, varnish plastic adhesive, insecticides, perfumes and pharmaceuticals. 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 -- Allyxycarb: Allyxycarb is a carbamate pesticide used mainly as an insecticide. 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Aluminum Phosphide: Aluminum Phosphide is a chemical used mainly as a rodenticide and fumigant for grains. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Amidithion: Amidithion is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Aminocarb: Aminocarb is a carbamate pesticide used mainly as an insecticide. 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Amiton: Amiton is a chemical once used as an insecticide and acaricide - it is no longer in use due to its nerve toxicity. The chemical is an organophosphorus compound and 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Amitraz: Amitraz is a chemical used mainly as a topical parasitic preventative in livestock and fruit trees. It is also used as an insect repellant and a prevention of mite infestation. The chemical is readily absorbed through the skin. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Amitrole: Amitrole is a herbicide. 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 -- Ammonium Nitrate: Ammonium Nitrate is a chemical used mainly in explosives, fireworks and fertilizers. 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 -- Aniline: Aniline is a chemical used mainly in the manufacture of perfumes, varnishes, resins, dyes, paint removers, herbicides, fungicides, explosives, solvents and photographic chemicals. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Anisidine (o,p-Isomers): Anisidine (o,p-Isomers)is a chemical used mainly in the production process of pharmaceuticals and azo-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 -- Antifreeze: Antifreeze is used in vehicles to prevent freezing or boiling over of the cooling system. The chemicals (methanol, ethylene and propylene glycol) in the antifreeze can cause severe poisoning symptoms if ingested. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Antimony: Antimony is a chemical often used as an alloy with other metals such as lead. It is used in solder, ammunition, pewter, sheet metal, pipe metal and cable sheaths. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Aparasin: Aparasin Aparasin. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. 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 -- Aphtiria: Aphtiria is a chemical insecticide used mainly to control scabies or lice. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. 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 -- Arsine: Arsine is a chemical used in the making of semiconductors and in the metal refining industry. It is considered a possible chemical agent in chemical warfare. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Athyl-Gusathion: Athyl-Gusathion is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Azinfos-methyl: Azinfos-methyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Azinfosethyl: Azinfosethyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Azinophos-methyl: Azinophos-methyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Azinphos: Azinphos is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Azinphos-ethyl: Azinphos-ethyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Azinphos-methyl: Azinphos-methyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Azinphosmetile: Azinphosmetile is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Azothoate: Azothoate is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Barthrin: Barthrin is a pyrethroid chemical used as an insecticide. The chemical is toxic to the nerve system. 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 -- Ben-Hex: Ben-Hex is a chemical insecticide used mainly to control scabies. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. 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 -- Bendiocarb: Bendiocarb is a carbamate pesticide used mainly in . 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Benfuracarb: Benfuracarb is a carbamate pesticide used mainly as an insecticide. 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Benhexol: Benhexol is a chemical insecticide used mainly to control scabies or lice. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. 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 -- Benoxafos: Benoxafos is a chemical pesticide used as an acaricide. The chemical is an organophosphorus compound and 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Benzene: Benzene is a chemical used mainly in gasoline fuel and as an industrial solvent. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Benzene hexachloride: Benzene hexachloride is a chemical insecticide. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. 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 -- Beta-cyfluthrin: Beta-cyfluthrin is a pyrethroid chemical used as an insecticide. The chemical is toxic to the nerve system. 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 -- Bexol: Bexol is a chemical insecticide used mainly to control scabies or lice. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. 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 -- Bifenthrin: Bifenthrin is a pyrethroid chemical used as an insecticide and acaricide. The chemical is toxic to the nerve system. 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 -- Bioallethrin: Bioallethrin is a pyrethroid chemical used as an insecticide. The chemical is toxic to the nerve system. 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 -- Bioehtanomethrin: Bioehtanomethrin is a pyrethroid chemical used as an insecticide. The chemical is toxic to the nerve system. 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 -- Biopermethrin: Biopermethrin is a pyrethroid chemical used as an insecticide. 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 -- Bioresmethrin: Bioresmethrin is a pyrethroid chemical used as an insecticide. 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 -- Bromates: Bromate is a chemical used mainly in perming solution neutralizers and in small amounts as a bread preservative. 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 -- Bromethalin: Bromethalin is a chemical used mainly in rodenticides. The chemical is toxic to the human nerve system. 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 -- Bromide: Bromide is a chemical used for many applications - flame retardant, industrial uses, pesticides, sanitary products, fumigants, medicines, dyes, photographic solutions and water purification. Bromides act as central nervous system depressants and the ingestion of excessive quantities can cause serious symptoms. 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 -- Bromophos: Bromophos is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Bromophos-ethyl: Bromophos-ethyl is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Bufencarb: Bufencarb is a carbamate pesticide used mainly as an insecticide. 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Butacarb: Butacarb is a carbamate pesticide used mainly as an insecticide. 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Butocarboxim: Butocarboxim is a carbamate pesticide used mainly as an insecticide. 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Butoxcarboxim: Butoxcarboxim is a carbamate pesticide used mainly as an insecticide. 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Butyl Alcohol: Butyl alcohol is a chemical used mainly in solvents and in pharmaceutical manufacturing processes. 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 -- Butylamines: Butylamines are chemicals used in a variety of manufacturing processes such as in the production of pesticides, pharmaceuticals, plastics, dyes, textiles and in leather tanning and photography. 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 -- Cadusafos: Cadusafos is a chemical pesticide used as an insecticide and nematicide. The chemical is an organophosphorus compound and 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Calcium Polysulfide: Calcium polysulfide is a chemical used mainly in antifungal treatments for trees. 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 -- Carbanolate: Carbanolate is a carbamate pesticide used mainly as an insecticide and acaricide. 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Carbaryl: Carbaryl is a carbamate pesticide used mainly as an insecticide and acaricide. 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Carbinoxamine: Carbinoxamine is a therapeutic treatment for allergic rhinitis. It is marketed under names such as Histex, Pediatiex and Carboxine. 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 -- Carbofuran: Carbofuran is a carbamate pesticide used mainly as an insecticide, nematicide and acaricide. 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Carbon Disulfide: Carbon Disulfide is a chemical used mainly in corrosion inhibitors, cold and nickel plating, photography applications and as a solvent in gums and resins. 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 -- Carbon Tetrachloride: Carbon tetrachloride is a chemical used mainly in grain fumigants, insecticides and in the production of fluorocarbons. Ingestion and other exposures to the chemical can cause various symptoms. The chemical is readily absorbed through the skin. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Carbophenothion: Carbophenothion is a chemical pesticide used as an insecticide and acaricide. The chemical is an organophosphorus compound and 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Carbosulfan: Carbosulfan is a carbamate pesticide used mainly as an insecticide and nematicide. 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. The chemical may be absorbed through the skin.
  • Chemical poisoning -- Castor oil: Castor oil is a type of vegetable oil often used in medicinal or therapeutic products that improve bowel functioning. However, excessive ingestion of castor oil can cause various symptoms.
  • Chemical poisoning -- Chloralose: Chloralose is a chemical used mainly in poisons for rodents and crows . 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 -- Chlordane: Chlordane is a poison use to control termites - is banned in the US and many other countries due to its harmful effects. Ingestion and other exposures to the chemical can cause various symptoms. The chemical is readily absorbed through the skin. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Chlordecone: Chlordecone is an insecticide used to control pests in crops such as bananas and tobacco. Ingestion and other exposures to the chemical can cause various symptoms. The chemical may be readily absorbed through the skin. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Chloresene: Chloresene is a chemical insecticide used mainly to control scabies or lice. The insecticide is considered moderately toxic to humans and acts as a central nervous system stimulant. 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.

Conditions listing medical symptoms: Coordination problems:

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

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Conditions listing medical complications: Coordination problems:

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

 

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