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Symptoms » Sexual symptoms » Glossary
 

Glossary for Sexual symptoms

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

  • 11q Partial Trisomy: A very rare genetic disorder caused by a duplication of part of chromosome 11q. The characteristic symptoms of the disorder are delayed growth before and after birth, mental retardation (varying severity) and skull and facial defects. The type and severity of symptoms that can occur are variable.
  • 17-Beta-hydroxysteroid dehydrogenase III deficiency: A rare disorder characterized caused by an enzyme (17-ketosteroid reductase) defect only in the testes which results in a lack of testosterone which is needed during the fetal stage to give males there physical characteristics.
  • 18p minus syndrome: A rare chromosomal disorder where a portion of chromosome 18 is missing which is characterized by mental and growth deficiencies, drooping upper eyelid and prominent ears. The type and severity of symptoms is determined by the amount of genetic material that is missing.
  • 3-Beta-HSD, Deficiency of: A rare condition where the deficiency of a particular enzyme (3-Beta-Hydroxysteroid Dehydrogenase) results in reduced levels of adrenal hormones - mineralocorticoids, glucocorticoids and sex steroids. The condition results in variable degrees of salt wasting and abnormal sexual organ development depending on the level of deficiency.
  • 3-Beta-Hydroxysteroid Dehydrogenase deficiency: A rare condition where the deficiency of a particular enzyme (3-Beta-Hydroxysteroid Dehydrogenase) results in reduced levels of adrenal hormones - mineralocorticoids, glucocorticoids and sex steroids. The condition results in variable degrees of salt wasting and abnormal sexual organ development depending on the level of deficiency.
  • 3-Beta-Hydroxysteroid Dehydrogenase, Type II, Deficiency of: A rare condition where the deficiency of a particular enzyme (3-Beta-Hydroxysteroid Dehydrogenase) results in reduced levels of adrenal hormones - mineralocorticoids, glucocorticoids and sex steroids. The condition results in variable degrees of salt wasting and abnormal sexual organ development depending on the level of deficiency.
  • 3?-hydroxysteroid dehydrogenase deficiency: A ver rare form of congenital adrenal hyperplasia involving a deficiency of 3?-hydroxysteroid dehydrogenase which results in reduced production of adrenal steroids (mineralocorticoids, sex steroids and glucocorticoids). The disorder can occur in classical, non-salt wasting and late-onset varieties.
  • 46,XX chromosome 7 deletion p13-p21: A chromosomal disorder where a small portion of chromosome 7 is deleted which results in a range of abnormalities.
  • 46,XX testicular DSD: A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY.
  • 46,XX testicular disorder of sex development: A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY.
  • 46,XY Gonadal Dysgenesis, Complete, SRY-Related: A rare disorder where a female has all the normal external femal characteristics but has non-functioning gonads. This means that no sex hormones needed for puberty are produced. This particular type is the result of a defect in the SRY gene located on chromosome Yp11.3.
  • 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.
  • 49,XXXXY syndrome: A rare sex chromosome abnormality where there are three extra copies of the X chromosome.
  • ACPS III: A rare genetic condition characterized by head and digital anomalies as well as other abnormalities.
  • Abdominal Cancer: Growth of abnormal cells (tumour) affecting the organs in the abdominal cavity; may be due to primary growth of a tumour or spread from another tumour (metastases, secondary tumour)
  • Abdominal pain that worsens with menses: also known as dysmenorrhea
  • Abdominal symptoms: Symptoms affecting the abdomen or digestive tract
  • Abidi X-linked mental retardation syndrome: A rare genetic disorder characterized by a number of physical abnormalities
  • Ablepharon macrostomia syndrome: A rare disorder involving a number of mainly physical abnormalities.
  • Abnormal enlargement of bladder: rapid increase in the size of the urinary bladder
  • Abnormal infrequent menstrual bleeding: also known as oligomenorrhea is the infrequent uterine bleeding episodes with intervals of more than 35 days
  • Abnormal uterine bleeding: The loss of blood from the uterus that varies from that which is considered normal
  • Abnormal vaginal bleeding: refers to vaginal bleeding at any time during the menstrual cycle other than normal menstruation
  • Abnormal vaginal bleeding in children: Abnormal vaginal bleeding in children is any kind of bleeding or hemorrhage from the vagina in a girl who has not yet reached menses or puberty.
  • Abnormal vaginal bleeding in pregnancy: Bleeding from the vagina during pregnancy that occurs after conception but before the onset of labour.
  • Abnormal vaginal discharge: Abnormal vaginal discharge includes any type of discharge from the vagina that is not expected or typical, is heavier than usual, is bloody, is more watery than usual, and/or has an unusual smell.
  • Abnormally decreased urination: known as oliguria
  • Abruptio placentae: A condition which is characterized by the premature detachment of the placenta from the uterus
  • Absence of vaginal bleeding: also called amenorrhea is the absence of menstruation in a women of reproductive age group. It maybe be primary or secondary
  • Absent menses: amenorrhea is the absence of menstruation
  • Abuse dwarfism syndrome: Retarded growth, intelligence and social behavior due to child abuse. The child abuse can take the form of mental or physical cruelty or neglect.
  • 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.
  • Achard-Thiers Syndrome: A rare hormonal disorder that occurs in diabetic postmenopausal women where body hair grows in a masculine manner. Hormonal therapy is used to correct the endocrine imbalance.
  • Achondroplasia: A rare disease characterized by abnormal bone growth which results in short stature with short arms and legs, large head and characteristic facial features.
  • 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.
  • Acquired Cystic Kidney Disease: Kidney disease causing kidney cysts.
  • Acquired angioedema: A rare disorder characterized by recurring episodes of swelling of parts of the skin or mucous membranes. Sometimes internal organs may be involved. The disorder occurs in patients with lymphoproliferative or autoimmune disorders which result in the dysfunction of a complex blood protein called C1 inhibitor.
  • Acquired angioedema, type 1: A rare disorder characterized by recurring episodes of swelling of parts of the skin or mucous membranes. Sometimes internal organs may be involved. The disorder occurs in patients with lymphoproliferative disorders which affects the function of a complex blood protein called C1 inhibitor.
  • Acquired angioedema, type 2: A rare disorder characterized by recurring episodes of swelling of parts of the skin or mucous membranes. Sometimes internal organs may be involved. Type 2 is an autoimmune disorder where patients develop autoantibodies which destroy the function of C1 esterase inhibitor.
  • Acquired prothrombin deficiency: A deficiency of prothrombin (vital for blood clotting) which is acquired through other conditions such as liver disease, anticoagulant drugs or vitamin K deficiency. The severity of symptoms is determined by the degree of deficiency.
  • Acro-pectoro-renal field defect: A very rare genetic syndrome characterized by abnormalities of the genital and urinary systems as well as the absence of chest muscles at birth.
  • Acrocephalopolydactyly -- Cardiac Disease -- Ear, Skin and Lower Limb Defects: A rare genetic condition characterized by head and digital anomalies as well as other abnormalities.
  • Acrocephalopolysyndactyly type III: A rare genetic condition characterized by head and digital anomalies as well as other abnormalities.
  • Acrofacial dysostosis -- ambiguous genitalia: A rare disorder characterized mainly by ambiguous genitals and abnormal development of bones in the face, jaw, hands and feet.
  • Acrofacial dysostosis Catania form: One of a group of disorders characterized by defective limb and facial development. The Catania form is very rare.
  • Acromegaly: An abnormal enlargement of the limbs due to increased secretion of growth hormone after the cessation of puberty
  • Actinomycosis: A chronic infection usually caused by an organism normally found in human bowels and mouths. The disease usually affects the face and neck and results in deep, lumpy abscesses that emit a grainy pus through multiple sinuses.
  • Acute (or transient) urinary incontinence: Acute (or Transient) Incontinence is caused by a new or recent medical problem that can be treated.
  • 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 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 chronic tailbone pain: pain due to lesions in the coccyx
  • Acute chronic vaginal pain: pathologies of the vagina
  • Acute diarrhoea: A sudden onset of diarrhoea
  • Acute epididymitis:
  • Acute erythroleukemia: A rare condition characterized by the presence of abnormal blood cells (erythroblastic precursors) in the bone marrow and blood. The condition is characterized by anemia and generally leads to the development of acute myelogenous leukemia. The acute form has more severe symptoms than the chronic form.
  • Acute herpes-like penile ulcers: formation of vesicles similar to the presentation in herpes
  • Acute herpes-like vaginal ulcers: formation of vaginal ulcers similar to the presentation in herpes
  • 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 kidney failure: The sudden and acute loss of kidney function
  • 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 oophoritis:
  • Acute pain from intercourse: also known as dyspareunia
  • Acute pain from intercourse in pregnancy: Acute pain from intercourse in pregnancy is the sudden onset of pain in the region of the vagina and pelvis, occurring during intercourse whilst pregnant.
  • Acute pelvic inflammatory disease:
  • Acute pelvic pain in children: Acute pelvic pain in children is a condition in which there is a sudden onset of pain or discomfort in the pelvis of a child.
  • Acute promyelocytic leukemia: A rare bone marrow cancer characterized by a lack of mature blood cells and excessive amounts of immature blood cells (promyelocytes).
  • Acute prostate blockage like symptoms: conditions which cause acute symptoms similar to that when there is a blockage to prostate secretions
  • Acute prostate pain symptoms: conditions which cause acute pain similar to that of pain due to a prostatic pathology
  • Acute prostate symptoms: acute symptoms related to the prostate includes painful micturition, hestiatancy and frequency of micturition
  • Acute prostate-related urinary dribbling: weak urinary stream
  • Acute prostate-related urinary symptoms: Symptoms include urinary frequency, urgency, urgency incontinence, voiding at night (nocturia), weak urinary stream, hesitency (needing to wait for the stream to begin), intermittency (when the stream starts and stops intermittently), straining to void, dysuria (burning sensation in the urethra), and dribbling
  • Acute prostate-related weak urinary stream: weak urinary stream
  • Acute prostatitis: An acute condition which affects the prostate which is the result of infammation
  • Acute respiratory distress syndrome, Infant: A breathing disorder that occurs in infants. The underdeveloped lungs fail to functioning adequately and the body becomes deprived of oxygen. The condition is more likely to affect premature infants and the greater the prematurity, the greater the risk.
  • Acute testicular pain in children: Acute testicular pain in children is the sudden appearance of pain or discomfort in the testicle or testicles of a child.
  • Acute torsion of testis:
  • Acute uterine pain: pathologies of the uterus which cause pain for a short duration
  • Acute uterine pain in pregnancy: Acute uterine pain in pregnancy refers to sudden onset of pain in the lower abdomen originating from the uterus in a woman who is pregnant
  • Adenine phosphoribosyltransferase deficiency: A rare genetic disorder where an enzyme (2, 8-dihydroxyadenine) deficiency results in urinary tract stone formation.
  • Adenocarcinoma, Clear Cell: A type of cancer that occurs mainly in the genitourinary tract and the cells that make up the tumor are clear. It is very rare and most cases occur in females whose mothers used a drug called DES (synthetic estrogen) while pregnant.
  • Adenomyosis: presence of ectopic endometrial tissue in the myometrium
  • Adenosarcoma of the uterus: A tumor that develops from the glands that line the uterus.
  • Adnexal and Skin Appendage Neoplasms: A type of tumour that develops on particular organs - eyes, skin and uterus. The tumors are usually benign but some may become malignant. The symptoms will vary depending on the location of the tumor and whether it is benign or malignant. These type of tumors tend to be most common in middle-aged women.
  • Adnexal tenderness: Tenderness of the appendages or secondary structures of the uterus.
  • Adolescent cataract and infertility syndrome: A rare syndrome characterized mainly by cataracts and infertility in male adolescents.
  • Adrenal Cancer: A malignant cancer that develops in the adrenal gland. The tumor may be nonfunctioning (does not produce hormones) or functioning in which case excessive levels of hormones can cause a variety of symptoms depending on which hormone is involved. Adrenal hormones made in the cortex (outer part of the gland) are aldosterone, corticosteroids and androgenic steroids. Adrenalin and noradrenalin are the hormones made in the medulla (central part of the adrenal gland).
  • Adrenal Cortex Diseases: Diseases of the adrenal cortex. Examples includes Addison's disease, Cushing's syndrome and adrenal fatigue.
  • Adrenal Cortex Neoplasms: A tumor that develops in the adrenal gland. The tumor may be nonfunctioning (does not produce hormones) or functioning in which case excessive levels of hormones can cause a variety of symptoms depending on which hormone is involved. Adrenal hormones made in the cortex (outer part of the gland) are aldosterone, corticosteroids and androgenic steroids.
  • Adrenal Hyperplasia, Congenital (General): Congenital adrenal hyperplasia is an inherited condition characterized by adrenal insufficiency. It is caused by a deficiency in an enzyme needed to produce certain adrenal hormones such as cortisol and aldosterone.
  • Adrenal adenoma, familial: A benign tumor that develops in the adrenal gland and tends to run in families. The tumor may be nonfunctioning (does not produce hormones) or functioning in which case excessive levels of hormones can cause a variety of symptoms depending on which hormone is involved. Adrenal hormones made in the cortex (outer part of the gland) are aldosterone, corticosteroids and androgenic steroids . Adrenalin and noradrenalin are the hormones made in the medulla (central part of the adrenal gland).
  • Adrenal gland hyperfunction: Excessive activity of the adrenal gland which causes excessive production of one or more adrenal hormones (aldosterone, corticosteroids, androgenic steroids, epinephrine and norepinephrine). The increased adrenal gland activity may be caused by an adrenal gland tumor or by excessive stimulation of the gland. Pituitary hormones stimulate adrenal gland activity.
  • Adrenal gland symptoms: Symptoms affecting the adrenal glands
  • Adrenal hyperplasia, congenital type 3: A group of disorders that occur when a deficiency of 21-hydroxylase impairs the normal process of making adrenal corticosteroids. The severity of the condition is variable depending on the degree of deficiency.
  • Adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency: A rare form of congenital adrenal hyperplasia characterized by a deficiency of 11-Beta-hydroxylase which results in excess androgen production and hypertension. The disorder can occur in virilizing, hypertensive and salt-wasting forms and symptoms may range from mild to severe.
  • Adrenal hypoplasia congenital, X-linked: A genetic disorder which affects the body tissues that produce hormones. It is characterized by underdeveloped adrenal glands which results adrenal insufficiency and hypogonadotrophic hypogonadism.
  • Adrenal incidentaloma: A tumor of the adrenal gland that is discovered incidentally while performing an imaging examination for reasons other than an adrenal tumor. The tumor may be asymptomatic or can causes excessive secretion of adrenal hormones and resulting symptoms. The tumor may also be malignant or benign.
  • Adrenocortical carcinoma: A condition which is characterized by malignancy which affects the adrenocortex.
  • Adrenoleukodystrophy: A rare hereditary metabolic disease that only occurs in male children and is characterized by adrenal atrophy and extensive cerebral demyelination causing progressive loss of mental functioning, aphasia, apraxia and sometimes blindness. The patient usually dies within 5 years.
  • Adult-onset Renal Failure: A progressive kidney disease characterized by the presence of high blood pressure.
  • Adverse reaction to chemical -- 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. Some people can suffer an adverse reaction to the chemical. The severity of symptoms varies depending on the amount of chemical involved and the route of exposure.
  • Aging: The medical conditions from getting older.
  • Agnathia-holoprosencephaly-situs inversus: A very rare disorder characterized by a small or absent jaw, developmental brain defect and internal organs situated on the wrong side of the body (situs inversus). The severity and range of symptoms is variable.
  • Ahumada-Del Castillo Syndrome: A form of secondary amenorrhea often resulting from a pituitary gland tumor. The condition causes galactorrhea and amenorrhea even when the patient is not pregnant.
  • Al Awadi syndrome: A rare syndrome characterized primarily by severe malformations involving the limbs and pelvis.
  • Al Awadi-Raas-Rothschild syndrome: A rare syndrome characterized primarily by severe malformations involving the limbs and pelvis. The exact type and severity of symptoms is variable. Most cases appear to occur in cases where the parents were related.
  • Alcock syndrome: A nerve disorder which causes pain in the pelvic, genital and perianal areas.
  • Alcohol abuse: Excessive alcohol as a symptom of other conditions
  • 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.
  • Alkaptonuria: A rare inherited metabolic disease characterized by homogentisic aciduria, arthritis and ochronosis. Symptoms include darkening of urine, alkinization due to overproduction of homogentisic acid, arthritis in the large joints and black ochronotic pigmentation of cartilage and collagen tissue. However, many of these symptoms may not occur until middle age. The condition may also be caused by chronic phenol poisoning.
  • Allen-Masters syndrome: Damage to muscle layers in the pelvis which allows the abnormally increased movement of the cervix. It often occurs after a traumatic surgical birth, induced abortion or excessive vaginal packing.
  • Allergic seminal vulvovaginitis: Vaginal inflammation following contact with semen after ejaculation.
  • Allergic tension-fatigue syndrome: Variable symptoms caused by food allergy.
  • Aloe poisoning: Aleo vera is often used on the skin to treat such things as burns and dermatitis. The sap from the leaves contain a chemical called anthraquinone glycoside which can cause skin irritation in susceptible people but can also cause poisoning symptoms.
  • Alpha thalassemia: Thalassemia is an inherited blood disorder characterized by abnormal synthesis of hemoglobin. Hemoglobin consists of two main protein chains called alpha and beta. Alpha thalassemia involves defects in one or more of the four genes required to make each ? protein chain. The main symptom is anemia, the severity of which can vary amongst patients depending on how many defective genes are involved.
  • Alpha thalassemia -- Hemoglobin H disease: Thalassemia is an inherited blood disorder characterized by abnormal synthesis of hemoglobin. Hemoglobin consists of two main protein chains called alpha and beta. Hemoglobin H disease involves defects in three of the four genes required to make each ? protein chain. The main symptom is moderate to severe anemia.
  • Alpha thalassemia major: Thalassemia is an inherited blood disorder characterized by abnormal synthesis of hemoglobin. Hemoglobin consists of two main protein chains called alpha and beta. Alpha thalassemia major is very rare involves defects in all of the four genes required to make each ? protein chain. The condition leads to infant death before or soon after birth.
  • Alport Syndrome: A rare hereditary disorder involving the progressive deterioration of parts of the kidney resulting in chronic kidney disease.
  • Alport syndrome -- mental retardation -- midface hypoplasia -- elliptocytosis: A rare syndrome characterized by the association of Alport syndrome, mental retardation, underdeveloped midface and a blood abnormality (elliptocytosis). Alport syndrome is an inherited condition involving progressive kidney damage and hearing loss.
  • Alport syndrome with macrothrombocytopenia: A rare inherited syndrome characterized by progressive kidney damage and hearing loss as well as macrothrombocytopenia.
  • Alport syndrome, dominant type: A rare syndrome characterized by kidney problems and hearing loss. The condition is inherited as a dominant trait.
  • Alport syndrome, recessive type: A rare syndrome characterized by kidney problems and hearing loss. The condition is inherited as a recessive trait.
  • Alsing syndrome: A rare syndrome characterized mainly by kidney problems, skeletal abnormalities and a hole in the coloboma of the eye.
  • Altered bladder habits: causes of retention
  • Altered bladder habits in pregnancy: Altered bladder habits in pregnancy are normal and consist of nocturia and frequency of micturition.
  • Ambiguous genitalia: Genitalia that is difficult to distinguish.
  • Ambiguous genitalia in children: Ambiguous genitalia in children include variations and/or combinations of genitalia in a child that makes it unclear if it is a boy or a girl.
  • Amelogenesis Imperfeca, Hypoplastic, and Nephrocalcinosis: A rare disorder involving abnormal tooth development and kidney problems.
  • Amenorrhea: Absence of menstrual periods.
  • Aminoaciduria: Increased amino acid levels in the urine which could indicate inborn metabolic disorders which may be caused by deficiencies in certain enzymes e.g. cystinuria.
  • Amitriptyline -- Teratogenic Agent: There is strong evidence to indicate that exposure to Amitriptyline during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Amitriptyline toxicity: The toxic reaction of the body to the substance, possibly via allergic reaction or overdose.
  • Ammonia-smelling urine: Ammonia-smelling urine refers to urine with an odor of ammonia.
  • Ammonia-smelling urine in children: Ammonia-smelling urine in children is urine with an abnormal smell of ammonia, often indicating a urinary tract infection in children.
  • Amoxapine toxicity: The toxic reaction of the body to the substance, possibly via allergic reaction or overdose.
  • Amphetamine -- Teratogenic Agent: There is strong evidence to indicate that exposure to Amphetamine during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
  • Amphetamine abuse: Use of the stimulant drugs known as amphetamines or "speed"
  • 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: A disease characterized by the accumulation of insoluble amyloid protein in tissues and organs which in turn affects the functioning of these tissues and organs.
  • Amyloidosis, familial visceral: A rare genetic disorder involving widespread amyloidosis (abnormal buildup of amyloid protein in tissues) which tends the affect the kidneys severely.
  • Anaesthesia complications: Complications that occur due to anaesthesia
  • Analgesic nephropathy syndrome: Kidney damage caused by excessive use of pain-killing drugs. Aspirin and phenacetin mixtures are the most common causes.
  • Andrade's syndrome: An inherited condition characterized by deposits of an abnormal protein called amyloid in various parts of the body including organs. The condition mainly involves neurological symptoms.
  • Androgen Insensitivity Syndrome: Females with male XY genetics but inability to respond to testosterone.
  • Androgen insensitivity syndrome, partial: A rare inherited condition where males are partially insensitive to the male hormones which results in varying degrees of feminization. The effect of the condition can range from the presence of normal female sexual characteristics to normal male sexual characteristics or a combination of both.
  • Andropause: A symptomatic decline in male androgens that may occur as men age.
  • 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.
  • Anemic -- hematuria syndrome: An epidemic disease in Argentina which has a prolonged recovery time but usually there are no complications. Symptoms vary between seasons so that affected patients suffer anorexia, vomiting, diarrhea and dehydration in summer but suffer reduced urination, excess blood, albumin and renal casts in the urine. Other symptoms occur irrespective of the season.
  • Angiopathy, hereditary, with nephropathy, aneurysms and muscle cramps: An inherited disorder characterized by kidney disease, aneurysms, blood vessel disease and muscle cramps which can last from seconds to minutes.
  • Angular cheilitis: This is an inflammation with maceration, exudation and fissure formation at the labial commissures
  • Aniridia -- absent patella: A rare genetic condition characterized by an abnormal or missing kneecap as well as the absence of the iris of the eye.
  • Anogenital pruritus: An itching located in the anal and genital regions
  • Anophthalmia/microphthalmia -- esophageal atresia: A rare disorder characterized by esophageal and genital defects as well as absent or very small eyes.
  • Anorchia: Congenital condition where one or both testes are absent.
  • Anorchidia: A rare birth defect where the testes are absent. The testes may regress at any stage of fetal development. The stage of fetal growth at which the testes regress will affect the presentation of the disorder at birth. The presentation at birth may range from varying degrees of genital ambiguity with streak gonads.
  • Anorexia: This is known as a lack of or loss of appetite for food
  • Anorexia Nervosa: A disorder where a distorted sense of body image leads to self-starvation to the point of death in some cases.
  • Anorexia nervosa, genetic types: There is mounting evidence that anorexia nervosa may be caused by genetic factors which when combined with psychosocial factors can increase a persons risk of developing the condition.
  • Antepartum Eclampsia: Antepartum eclampsia is the development of seizures or coma in pregnant women suffering from high blood pressure. Antepartum means that it occurs before delivery. Eclampsia is a serious condition which requires urgent medical treatment. Eclampsia may be associated with moderate as well as significant increases in blood pressure. The blood pressure can return to normal after delivery or may persist for a period of time.
  • Anterior pituitary hyperhormonotrophic syndrome: A syndrome characterized by the excessive production of various hormones (gonadotrophic, thyrotrophic, lactotrophic and pancreatrophic hormone).
  • Anti-glomerular basement membrane antibody-mediated disease: A kidney disorder involving varying degrees of kidney impairment. Severe cases lead to kidney failure whereas mild cases have normal kidney function.
  • Anuria: Anuria is a lack of urine.
  • Anxiety: Excessive worry, anxiety, or fear.
  • Anxiety disorder: A mental condition that is characterized by anxiety and avoidance behaviours
  • Aortic arches defect: A defect in the top part of the aorta (aortic arch) that consists of several arterial branches. There is a variety of defects that can occur and symptoms will be determined by the particular defect involved. Possible types of defects includes aortic coarctation and aortic arch hypoplasia.
  • Aplastic anemia: A blood disorder where the bone marrow produces insufficient new blood cells.
  • Apparent Mineralocorticoid Excess, type 2: A form of inherited high blood pressure that starts during early childhood. The condition is caused by a genetic defect which results in an inborn error of metabolism of peripheral cortisol. Type 2 causes similar symptoms to type 1 but the urinary steroid levels are different.
  • Apparent mineralocorticoid excess: A form of inherited high blood pressure that starts during early childhood. The condition results from a genetic defect which causes impaired metabolism of cortisol.
  • Appendiceal tumor: A tumor of the appendix. The condition is often misdiagnosed as acute appendicitis. The cancer usually metastasizes from other sites and rarely starts in the appendix.
  • Appendix cancer: Cancer of the appendix. The cancer usually metastasizes from other sites and rarely starts in the appendix.
  • 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.
  • Argentinean hemorrhagic fever: An infectious disease caused by the Junin virus. Transmission can occur through contact with infected rodent (usually the corn mouse) urine, feces or saliva. The incubation period lasts from one to two weeks. The disease is most common in rural workers in Argentina.
  • Aristolochic Acid poisoning: Aristolochic acid is derived from a forest herb from the Aristocholochia family. It is often used in herbal preparations such as Aristolochia Fang Ch, Bragantia and Asarum. It is usually used in herbal preparations to promote weight loss. The substance is believed to cause kidney failure and urinary tract cancer.
  • Arnold-Chiari Malformation (Type 1): A rare malformation where the base of the brain enters into the upper spinal canal.
  • Aromatase deficiency: A congenital deficiency of the enzyme called aromatase which is needed to convert androgens to estrogens.
  • Arthritis-related enthesitis: Inflammation of the entheses due to arthritis. The enthuses is the site at which the tendon or ligament attaches to the bone.
  • Arthrogryposis multiplex congenita, distal, X-linked: A rare condition characterized by the presence of contractures at birth as well as various other anomalies. The condition is X-linked.
  • Asherman Syndrome: A condition where adhesions form inside the uterus because of uterine surgery or infection. The adhesions may cause menstruation to cease and/or infertility.
  • Asherman's syndrome: Scarring and adhesions that develop in the uterus and can result in menstrual and fertility problems.
  • Ataxia, spastic, 3, autosomal recessive: A recessively inherited disorder characterized mainly by spasticity and ataxia.
  • Athabaskan severe combined immunodeficiency: A severe immunodeficiency disorder found in Navajo and Apache populations.
  • Atherosclerosis, premature -- deafness -- diabetes mellitus -- photomyoclonus -- nephropathy -- degenerative neurologic disease: A rare syndrome characterized mainly by deafness, diabetes, epilepsy, kidney disease and premature hardening of the arteries.
  • Atrophic vaginitis: Type of vaginitis usually related to aging and menopause
  • Attenuated congenital adrenal hyperplasia: A late onset form of congenital adrenal hyperplasia where insufficient adrenal corticosteroids are produced by the body due to the deficiency of a particular chemical. The severity of symptoms varies from person to person and onset may occur as early as childhood.
  • Aureobasidium pullulans exposure: Aureobasidium pullulans is a species of fungus which is capable of causing a variety of diseases in humans. The fungus is most often found in damp places either inside the home or in the environment. It is often pinkish or blackish. It is a rare cause of disease and is more likely to occur in immunosuppressed patients. It can cause infection in just about any part of the body depending on the nature of the exposure (inhalation, wound, ingestion etc.) and as such the type and severity of symptoms can vary considerably.
  • Autoimmune Endometriosis: An endometriosis that is caused by an autoimmune reaction
  • 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 Hepatitis: Liver inflammation caused due to autoimmune processes where the body's immune system attacks the liver.
  • Autoimmune Myelopathy: A disturbance functionally or pathological change in the spinal cord
  • Autoimmune Thrombocytopenia: Autoimmune disorder causing a lack of blood platelets.
  • Autoimmune oophoritis: An autoimmune condition where the body's own immune system attacks the ovaries and causes them to become inflamed. It can lead to ovarian function stopping prematurely.
  • Autoimmune orchitis: A inflammation of the testicles caused by an autoimmune reaction
  • Autoimmune thyroid disease associated Celiac Disease: Patients with autoimmune thyroid disease are more susceptible to developing celiac disease than the average population. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
  • Autonomic dysfunction: disease or malfunction of the autonomic nervous system.
  • Autonomic neuropathy: A condition which is characterized by a functional disturbance or pathological change in the autonomic nervous system
  • Autosomal Recessive Polycystic Kidney Disease: Severe form of PKD, a genetic kidney disease.
  • Autosomal dominant polycystic kidney disease: Genetic kidney disease causing kidney cysts.
  • Axial osteosclerosis: A rare bone abnormality involving patches of increased bone density which tend to occur in the spine, pelvis and the ball part of the hip joint.
  • Azoospermia: Total lack of sperm in ejaculate
  • Azotemia, familial: A rare condition where high serum urea level is inherited in a familial pattern. The high level of urea occurs despite normal kidney function.
  • BEEC: A rare syndrome characterized by a birth defect where the bladder is inside out and protrudes from the lower abdominal wall. The urethra and genitals are also abnormally formed. The degree of malformation is variable.
  • BXO: Skin condition of the penis which can effect the glans, prepuce or urethra.
  • Back Impairment: An impairment of the function of the back
  • Back conditions: A group of conditions that affect the back
  • Back tumour: The presence of tumour growth in the vertebra, whether due to primary malignancies e.g. leukaemic or myeloma infiltration of the bone marrow, or due to secondary metastases from another site e.g. lung or breast.
  • Bacterial endocarditis: Infection and inflammation of the inner layers of the heart, most commonly the valves cause by bacteria.
  • Bacterial prostatitis: Bacterial prostatitis is a bacterial inflammation of the prostate gland, in men.
  • 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.
  • Bacterial vaginosis in pregnancy:
  • Balanitis: Inflammation of the glans (or head) of the penis.
  • Balanitis xerotica obliterans: A chronic, progressive skin condition involving sclerosis and atrophic processes of the penis.
  • Baneberry poisoning: Baneberries are toxic and can cause a skin reaction on contact or various poisoning symptoms.
  • Bannayan-Zonana syndrome: A rare genetic disorder characterized by macrocephaly, intestinal polyposis, pigmentation of penis and benign tumor-like growths.
  • Bardet-Biedl Syndrome: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities.
  • Bardet-Biedl syndrome, type 1: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 1 is caused by a defect in chromosome 11q13.
  • Bardet-Biedl syndrome, type 10: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 10 is caused by a defect in chromosome 12q.
  • Bardet-Biedl syndrome, type 11: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 11 is caused by a defect in chromosome 9q33.1.
  • Bardet-Biedl syndrome, type 12: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 12 is caused by a defect in chromosome 4q27.
  • Bardet-Biedl syndrome, type 2: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 2 is caused by a defect in chromosome 16q21.
  • Bardet-Biedl syndrome, type 3: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 3 is caused by a defect in chromosome 3p12-q13.
  • Bardet-Biedl syndrome, type 4: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 4 is caused by a defect in chromosome 15q22.3.
  • Bardet-Biedl syndrome, type 5: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 5 is caused by a defect in chromosome 2q31.
  • Bardet-Biedl syndrome, type 6: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 6 is caused by a defect in chromosome 20p12.
  • Bardet-Biedl syndrome, type 7: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 7 is caused by a defect in chromosome 4q27.
  • Bardet-Biedl syndrome, type 8: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 8 is caused by a defect in chromosome 14q32.11.
  • Bardet-Biedl syndrome, type 9: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 9 is caused by a defect in chromosome 7p14.
  • Barraquer-Simons syndrome: A rare disorder that occurs in children and involves the progressive loss of fat layers under the skin which affects the face first and then spreads to the chest region and limbs.
  • Bartholin's abscess: Abscess in a small vaginal gland
  • Bartholin's cyst: Cyst in a small vaginal gland
  • Bartter Syndrome: A rare genetic disorder of kidney metabolism characterized by reduced blood acidity and low potassium levels.
  • Bartter Syndrome type 4: Bartter syndrome is a rare disorder where abnormal kidney metabolism results in low blood acidity an potassium levels. Type 4 also involves sensorineural deafness.
  • Bartter Syndrome type 4A: Bartter syndrome is a rare disorder where abnormal kidney metabolism results in low blood acidity an potassium levels. Type 4A also involves sensorineural deafness.
  • Bartter Syndrome type 4B: Bartter syndrome is a rare disorder where abnormal kidney metabolism results in low blood acidity an potassium levels. Type 4B also involves sensorineural deafness.
  • Bartter's syndrome, antenatal type 1: A rare genetic kidney disorder that causes hypokalemia. A defect in the NKCC2 gene impairs the functioning of the Na-Cl cotransporter and leads to electrolyte imbalance. The rate of death is high prior to diagnosis.
  • Bartter's syndrome, type 3: A rare condition characterized by an electrolyte imbalance caused by mutations of the chloride channel gene (ClCNKb). It differs from Bartter's syndrome type I and type II in the absence of nephrocalcinosis. The severity of the condition is greatly variable.
  • Bartters syndrome, antenatal , type 2: A rare genetic kidney disorder that causes hypokalemia. A defect in the ROMK gene impairs the ATP-regulated potassium channel functioning and leads to electrolyte imbalance.
  • 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.
  • Bassoe syndrome: A very rare syndrome characterized primarily by hypogonadism, cataracts during infancy and muscle weakness.
  • Bearn-Kunkel syndrome: A type of autoimmune liver disease characterized by liver damage, very high blood gammaglobulin levels and increased plasma cells.
  • Bedwetting in children: Bedwetting in children is the inability to control urination during sleep in a child who is old enough to be toilet trained.
  • Behcet's syndrome: Recurring inflammation of small blood vessels affecting various areas.
  • Bence Jones Proteins: The presence of free light chains in the urine
  • Bence jones protein: Bence Jones protein is a type of abnormal protein that may be found in the urine associated with certain conditions and diseases that produce high levels of protein in the urine.
  • Benign Prostate Hyperplasia: Non-cancerous prostrate enlargement common with aging
  • Benign familial hematuria: A rare inherited kidney disorder characterized by periods of blood in the urine. The kidney is still able to function normally.
  • Benign mucosal pemphigoid: A rare chronic disease involving blistering and scarring of the mucous membranes especially in the mouth and conjunctiva of the eye.
  • Benign ovarian cyst:
  • Benign prostate hypertrophy: Non-cancerous prostrate enlargement common with aging
  • Bent penis: Abnormal bending or curvature of the penis
  • Bentham-Driessen-Hanveld syndrome: A rare syndrome characterized mainly by the association of undescended testes, long thin fingers and mental retardation.
  • Besnier-Boeck-Schaumann disease: A rare disease where inflammatory granular nodules form in various organs.
  • Beta Thalassemia intermedia: Thalassemia is an inherited blood disorder characterized by abnormal synthesis of hemoglobin. There are two subtypes of the disorder (alpha and beta) depending on what portion of the hemoglobin is abnormally synthesized. Beta Thalassemia intermedia involves defects in both of the two genes required to make each ? protein chain. The condition causes varying degrees of moderate anemia.
  • Beta thalassemia: Thalassemia is an inherited blood disorder characterized by abnormal synthesis of hemoglobin. Hemoglobin consists of two main protein chains called alpha and beta. Beta thalassemia involves defects in one or more of the two genes required to make each ? protein chain. The main symptom is anemia, the severity of which can vary amongst patients depending on how many defective genes are involved.
  • Biemond syndrome type 2: A rare inherited condition characterized by mental retardation, obesity, polydactyly and underdeveloped genitals.
  • Bilateral adnexal tenderness: grave gynaecological complication
  • Bile acid synthesis defect, congenital, 2: A defect which prevents the body from making bile acid which results in progressive liver disease. The defect is a deficiency of a particular enzyme (cholestasis with delta(4)-3-oxosteroid 5-beta-reductase) needed to make bile acid.
  • Bile acid synthesis defect, congenital, 4: A defect which prevents the body from making bile acid which results in progressive liver disease.
  • Bile acid synthesis defects: A defect which prevents the body from making bile acid which results in progressive liver disease.
  • Bile acid synthesis defects, congenital, 1: A defect which prevents the body from making bile acid which results in progressive liver disease. The defect is a deficiency of a particular enzyme (3-beta-hydroxy-delta-5-C27-steroid oxidoreductase) needed to make bile acid.
  • Bile acid synthesis defects, congenital, 2: A defect which prevents the body from making bile acid which results in progressive liver disease. The defect is a deficiency of a particular enzyme (cholestasis with delta(4)-3-oxosteroid 5-beta-reductase) needed to make bile acid.
  • Bile acid synthesis defects, congenital, 3: A defect which prevents the body from making bile acid which results in progressive liver disease. The defect involved a deficiency of 7-alpha-hydroxylase which is an enzyme needed to prevent the accumulation of 27-hydroxycholesterol which is toxic to the liver.
  • Bile acid synthesis defects, congenital, 4: A defect which prevents the body from making bile acid which results in progressive liver disease.
  • Bile duct cysts: The formation of a cyst (dilation or swelling) in the bile duct which can obstruct the flow of bile and result in jaundice.
  • Biliary Atresia: A rare condition that can affect newborns where the bile duct that carries the bile from the liver to the small intestine is blocked or missing.
  • Biliary atresia, intrahepatic, syndromic form: Congenital obstruction of the passages in the liver that carry bile. The syndromic form is associated with other congenital abnormalities such as heart and visceral defects.
  • Biliary hypoplasia: An underdeveloped biliary duct system which is involved in transporting bile. The bile ductules may be completely absent or be fewer in number than normal.
  • Biliary tract cancer: Cancer that develops in the gallbladder or bile ducts.
  • Bindewald-Ulmer-Muller syndrome: A rare syndrome characterized mainly by a heart defect, and mental and growth retardation.
  • 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.
  • Bipolar disorder: Cycles of mania and depression; commonly called "manic-depression".
  • Bipolar disorder I: Bipolar I disorder is a mood disorder that is characterized by at least one manic or mixed episode. Most people with bipolar I disorder also suffer from episodes of depression.
  • Birth control pill poisoning: Birth control pill contain hormones such as estrogen and progestin and excessive ingestion of the pills can result in relatively minor symptoms - usually there are no serious problems associated with the ingested of many birth control pills at one time. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Birth symptoms: Symptoms related to childbirth.
  • Black urine in children: Black urine in children refers to urine that is black in color in children.
  • Black widow spider envenomation: The black widow spider bite is toxic to the nerves and can cause serious symptoms. The black widow spider is most commonly found in North America.
  • Bladder burning sensation: Burning urination pain due to inflammatory bladder conditions.
  • Bladder cancer: Bladder cancer refers to any of several types of malignant growths of the urinary bladder. It is a disease in which abnormal cells multiply without control in the bladder.
  • Bladder conditions: Any condition affecting the bladder
  • Bladder distention: A condition which is characterized by anatomical distention of ones bladder
  • Bladder diverticulum: A defect where a part of the bladder lining forms a pouch in the muscle wall of the bladder. The defect may be congenital or acquired through conditions such as infection and urinary tract obstruction. The size of the diverticulum will determine the severity of the disorder with mild cases being asymptomatic.
  • Bladder fullness: distension of the lower central portion of the abdomen
  • Bladder immaturity syndrome: Urinary incontinence that occurs in young girls. Urine leakage can occur during the day or night and can sometimes be due to urinary tract infection.
  • Bladder incontinence: The inability to control ones bladder function
  • Bladder infection: Infection of the bladder.
  • Bladder infections: The occurrence of bacterial or other infections of the bladder
  • Bladder infections in pregnancy: Bladder infections in pregnancy cause pain in the suprapubic area, burning pain with micturition, urinary frequency, and are sometimes associated with pyelonephritis.
  • Bladder inflammation: A condition which is characterized by inflammation of the epithelial lining of the bladder
  • Bladder lump: Irregular small swelling in the bladder.
  • Bladder obstruction: Bladder obstruction can be acute or chronic.
  • Bladder pain: Pain affecting the bladder
  • Bladder pain in pregnancy: Bladder pain in pregnancy is usually caused by a urinary tract infection.
  • Bladder papilloma: Benign tumor in the bladder
  • Bladder redness: Erythematous inflammation of the urinary bladder due to infection.
  • Bladder swelling: Bladder swelling can be acute or chronic in nature.
  • Bladder symptoms: Symptoms related to the bladder and urination.
  • Bladder symptoms in pregnancy: Bladder symptoms in pregnancy are usually represented by pain in the suprapubic area, burning pain with micturition, urinary frequency, and are sometimes associated with pyelonephritis.
  • Bladder ulcer: Break in the continuity of the lining mucous membrane of the bladder.
  • Bladder weakness: Weakness in the detrusor muscle contractility.
  • Bleeding after sex: Vaginal bleeding after sexual intercourse
  • Bleeding that occurs after a woman has stopped menstruating: postmenopausal bleeding
  • Blepharophimosis, Ptosis, Epicanthus Inversus Syndrome: A rare genetic disorder characterized by inner canthal folds, lateral displacement of inner canthi and drooping upper eyelid. The severity of symptoms is variable. There are two subtypes of the condition: Type 2 involves eye anomalies as well as female fertility problems whereas type 1 only involves the eye anomalies.
  • Blepharophimosis, Ptosis, Epicanthus Inversus Syndrome, type 1: A rare genetic disorder characterized by inner canthal folds, lateral displacement of inner canthi and drooping upper eyelid. The severity of symptoms is variable. There are two subtypes of the condition: Type 2 involves eye anomalies as well as female fertility problems whereas type 1 only involves the eye anomalies.
  • Blepharophimosis, ptosis, epicanthus inversus: A rare genetic disorder characterized by inner canthal folds, lateral displacement of inner canthi and drooping upper eyelid.
  • Blepharoptosis -- aortic anomaly: A rare disorder characterized mainly by the presence of droopy upper eyelids and an abnormal aorta.
  • Blethen-Wenick-Hawkins syndrome: A rare syndrome characterized mainly by short stature, skeletal abnormalities and reduced pituitary gland functioning.
  • Blood in urine: Hematuria is blood in the urine.
  • Blood in urine in children: Blood in urine in children is a condition in which there is visible blood or microscopic blood in the urine of a child.
  • Bloody diarrhea: Diarrhea with blood in stool
  • Bloody ejaculation: Blood appearing in the ejaculate after male ejaculation
  • Bloody semen: Blood appearing in ejaculated semen
  • Bloody vaginal discharge: discharge from the vagina other than normal menstruation
  • Bloody vaginal discharge in pregnancy: Bloody vaginal discharge in pregnancy refers to the loss of blood from the vagina whilst pregnant. This blood is often found on the toilet paper, in the toilet bowl or after sexual intercourse. The blood loss may or may not be accompanied by other symptoms such as pain.
  • Bloom Syndrome: A rare genetic inherited genetic disorder which mainly affects Ashkenazic Jewish people and is characterized by short stature, malar hypoplasia, and a telangiectatic erythema of the face.
  • Blue Diaper Syndrome: A rare metabolic disorder characterized by vision problems, bluish urine, fever and digestive anomalies.
  • Blue urine: Blue coloration of the urine
  • Blue urine in children: Blue urine in children is a condition in which the urine is blue.
  • Boggy enlarged prostate: enlarged painful prostate
  • Boichis syndrome: A rare syndrome involving nephronophthisis (progressive destruction of kidney tissue) from birth which leads to kidney failure and liver fibrosis.
  • Bolivian hemorrhagic fever: An infectious disease that occurs in Bolivia and is caused by the Machupo virus. Transmission can occur through contact with infected rodent (Calomys callosus) droppings. The incubation period lasts from one to two weeks.
  • Borderline Personality Disorder: Mental condition with behavioral and emotional problems.
  • Borjeson Syndrome: A rare genetic disorder characterized by severe mental deficiency, large ears, hypogonadism and other abnormalities.
  • Bosma-Henkin-Christiansen syndrome: A rare syndrome characterized mainly by a reduced sense of smell, an underdeveloped nose and hypogonadism.
  • Botulism food poisoning: Extremely dangerous food poisoning requiring medical attention, but not always recognized because of its non-abdominal symptoms.
  • Boucher-Neuhauser syndrome: A very rare disorder characterized by spinocerebellar ataxia, eye abnormalities and a failure of the pituitary to stimulate gonadal development during puberty.
  • Bowel incontinence: Loss of full control of the bowel
  • Brachycephalofrontonasal dysplasia: A very rare syndrome characterized primarily by widely spaced eyes and other head and face abnormalities.
  • Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia: A rare syndrome characterized mainly by short digits, extra digits and a small or absent shin bone.
  • Brain -- bone -- fat: A rare inherited disease characterized by bone cysts and progressive presenile dementia.
  • Breakthrough bleeding: Breakthrough bleeding includes any type of mild to severe bleeding or hemorrhaging that occurs after initial bleeding has stopped.
  • Breisky disease: A progressive wasting disease of the vulva that occurs in postmenopausal women and is probably caused by hormonal imbalance.
  • Brenner tumor of the vagina: A Brenner tumour usually occurs in the ovaries but can sometimes occur in the vagina. The tumor is generally benign.
  • Brewery urine odor in children: Brewery urine odor in children refers to an abnormal brewery type smell of a child's urine.
  • 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.
  • Bright's Disease: A condition where the parts of the kidneys that are responsible for filtering become inflamed and results in blood and proteins accidentally leaking into the urine. The condition can occur after certain infections and serious kidney dysfunction can result in severe or chronic complications.
  • Bronchiectasis -- oligospermia: A rare syndrome characterized by the association of bronchiectasis (enlarged bronchial airways) and a defect in the sperm ducts which affects the number of sperm produced. Patients suffer frequent bacterial infections.
  • Brown Recluse spider poisoning: The Brown Recluse spider is poisonous and is found mainly in southern and central areas of the US.
  • Brown snake poisoning: The Brown snake is a poisonous Australian snake. They are considered one of the most venomous snakes in the world and their bite can result in death without prompt medical attention. The snake venom contains toxins which affect the blood and nerve systems. Children tend to suffer more severe symptoms due to their smaller body size.
  • Brown urine: The occurrence of brown urine
  • Brudzinski's sign: A symptom which occurs in meningitis when flexion of the neck causes flexion of the hip and knee
  • Bulimia nervosa: Eating disorder with binging (overeating) and purging (vomiting).
  • Burning during urination: The experience of burning sensation when urinating
  • Burning during urination in pregnancy: Burning during urination refers to discomfort when urinating in a woman who is pregnant.
  • Burning micturition: Burning micturition is an uncomfortable or painful burning sensation in the urethra while urinating.
  • Burning micturition in males: Burning micturition in males is a condition in which a male experiences an uncomfortable or painful burning sensation in the urethra while urinating.
  • Burning on urination in female children: Burning on urination in female children occurs when a girl experiences stinging or burning pain when urinating.
  • Burning on urination in male children: Burning on urination in male children occurs when a boy experiences stinging or burning pain when urinating.
  • Burning urination in female children: Burning urination in female children is a condition in which a girl experiences burning in the urethra while urinating.
  • Burning urination in male children: Burning urination in male children refers to a boy who experiences burning in the urethra while urinating.
  • Burning urination in pregnancy: Burning urination in pregnancy is a condition in which a pregnant woman has burning in the urethra while urinating.
  • Burning when urinating: burning micturition is a classical presentation of infection
  • Burning when you urinate: burning micturition is a classical presentation of infection
  • Byler Disease: A rare inherited conditions where bile is unable to drain from the liver where it builds up and causes progressive liver damage. The conditions has an early onset and usually leads to end-stage liver disease by the end of the second decade.
  • Bywaters' syndrome: A trauma or accident involving the crushing of soft tissues and associated symptoms. Severe cases can result in death.
  • C1esterase deficiency: C1esterase deficiency is a condition characterized by swelling under the skin or mucosal tissue - the skin, respiratory tract or gastrointestinal tract may be affected. The condition may be inherited or acquired. Symptoms tend to develop over a few days and then abate after two to five days. Swelling attacks may occur fairly regularly e.g. weekly or sporadically e.g. once or twice a year.
  • CCFDN: A rare, recessively inherited syndrome characterized by cataracts during infancy, unusual facial appearance and neuropathy.
  • CDG syndrome type I: A rare genetic disorder where the body is unable to synthesize glycoproteins which results in multisystem problems.
  • Calcification of basal ganglia with or without hypocalcemia: Calcification of a part of the brain called the basal ganglia. That calcification may be associated with conditions such as hypothyroidism, cytomegalovirus, and AIDS or may occur for no apparent reason. The severity of the condition may vary greatly from asymptomatic to neurological, psychiatric and movement disorders. The disorder may also progress at variable rates or remain stable depending on the underlying disease process.
  • Calloso-genital dysplasia: A rare syndrome characterized by the total absence of the brain structure that connects the two halves of the brain (corpus callosum) as well as absent menstruation and coloboma.
  • Camera-Marugo-Cohen syndrome: A rare syndrome characterized mainly by mental retardation, muscle weakness, obesity and an asymmetrical body.
  • Campylobacter fetus infection: Campylobacter fetus is a food borne bacterial infection which may vary in severity from mild to severe. The bacteria are opportunistic and mainly affect debilitated patients but can also occur in healthy patients. Abortion due to blood infection in the fetus can occur in pregnant women who become infected. The infection is less likely to cause gastrointestinal symptoms such as diarrhea than other Campylobacter infections but is prone to causing infection in other parts of the body such as the appendix, abdominal cavity, central nervous system (meningitis), gallbladder, urinary tract and blood stream. Cattle and sheep are the main source of this bacteria.
  • Campylobacter jejuni infection: Campylobacter jejuni infection is a common food borne bacterial infection which may vary in severity from mild to severe. Death can occur in severe cases but tends to occur in patients with other existing illnesses such as HIV, cancer or liver disease. The infection can in rare cause infection in other parts of the body such as the appendix, abdominal cavity, central nervous system (meningitis), gallbladder, urinary tract and blood stream. Undercooked chicken is the main source of infection.
  • Camurati-Engelmann Disease: A very rare genetic disease thickening of areas of bone causing pain, weakness and wasting. Usually affects the legs during childhood. Also called diaphyseal dysplasia.
  • Cancer: Abnormal overgrowth of body cells.
  • Candidiasis: Fungal infection of moist areas such as mouth or vagina
  • Caramel urine odor in children: Caramel urine odor in children is a condition in which the urine has an abnormal caramel smell.
  • Carbohydrate deficiency glycoprotein syndrome type II: Congenital disorders of glycosylation is a group of very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 2 is caused by a genetic defect which involves the gene for a particular enzyme (Golgi localized N-acetyl-glucosaminyltransferase II). Type 2 tends to have more severe psychomotor retardation than type 1 but there is no peripheral neuropathy or underdeveloped cerebellum.
  • Cardiocranial syndrome: A rare syndrome characterized mainly by heart and skull abnormalities.
  • Cardiomyopathy -- hypogonadism -- metabolic anomalies: A rare syndrome characterized mainly by heart muscle disease, hypogonadism, blindness, deafness and metabolic anomalies. Puberty was normal despite the hypogonadism.
  • Cardiomyopathy, Alcoholic: A weakened heart mucle due to excessive alcohol consumption. Symptoms are usually not evident until the heart becomes severely damaged.
  • Cardiomyopathy, hypogonadism, collagenoma syndrome: A rare inherited condition characterized primarily by skin nodules. The skin nodules may be associated with organ system involvement resulting in a variety of other symptoms.
  • Carnitine Palmitoyl Transferase II Deficiency: A very rare inherited deficiency of a particular enzyme (Carnitine palmitoyl transferase 1) prevents fatty acids being transported to the part of the cell that converts it to energy. There are two main subtypes of the disorder with each involving a slightly different form of the enzyme. Type I can be readily managed through diet. Type II has three subtypes: the myopathic form affects mainly the muscles; the hepatocardiomuscular form affects the liver and heart muscle; and the lethal neonatal form affects muscles and organs and usually results in death during the first year of life.
  • Carnitine palmitoyl transferase 2 deficiency: A very rare inherited deficiency of a particular enzyme (Carnitine palmitoyl transferase) which prevents fatty acids being transported to the part of the cell that converts it to energy. There are two main subtypes of the disorder with each involving a slightly different form of the enzyme. Type I can be readily managed through diet. Type II has three subtypes: the myopathic form affects mainly the muscles; the hepatocardiomuscular form affects the liver and heart muscle; and the lethal neonatal form affects muscles and organs and usually results in death during the first year of life.
  • Carnitine palmitoyl transferase II deficiency, infantile hepatocardiomuscular type: A very rare metabolic disorder where deficiency of a particular enzyme (CPT II) prevents muscle fats being converted to energy. The infantile form of this disease affects the muscles and the liver and heart.
  • Carnitine palmitoyl transferase II deficiency, lethal neonatal form: A very rare metabolic disorder where deficiency of a particular enzyme (CPT II) prevents muscle fats being converted to energy. The lethal neonatal form affects various organs as well as the muscles and death usually occurs during the first year of life.
  • Carnitine palmitoyl transferase II deficiency, myopathic: A very rare metabolic disorder where deficiency of a particular enzyme (CPT II) prevents muscle fats being converted to energy. Prolonged exercise can cause an episode of muscle symptoms. The myopathic form of the condition is the least severe and tends to affect only the muscles.
  • Carnitine palmitoyl transferase deficiency: A very rare inherited deficiency of a particular enzyme (Carnitine palmitoyl transferase) which prevents fatty acids being transported to the part of the cell that converts it to energy. There are two main subtypes of the disorder with each involving a slightly different form of the enzyme. Type I can be readily managed through diet. Type II has three subtypes: the myopathic form affects mainly the muscles; the hepatocardiomuscular form affects the liver and heart muscle; and the lethal neonatal form affects muscles and organs and usually results in death during the first year of life.
  • Cast syndrome: Obstruction of the third part of the duodenum by an artery following the use of a body plaster cast or a Bradford frame.
  • Cataract -- intellectual deficit -- anal atresia -- urinary defects: A very rare syndrome characterized mainly by cataracts, mental retardation and genitourinary tract abnormalities and absent anal opening.
  • Cataract deafness hypogonadism: A very rare syndrome characterized mainly by deafness, cataracts and a deficiency of sex hormone production.
  • Catastrophic Antiphospholipid Syndrome: A very rare disorder where the blood clotting system becomes dysfunctional and clots too easily due to the abnormal presence of antphospholipid antibodies. It results in blood flow blockages to various body organs. It is possible that the condition has autoimmune origins. The disorder is often triggered by infections, certain drugs (e.g. anticoagulants), minor surgery and hysterectomy.
  • Caterpillar complication poisoning: The spines on certain caterpillars can cause a skin reaction as well as systemic symptoms if ingested. The nature of the symptoms vary depending on the species of caterpillar involved. Some only produce skin reactions whereas others can produce systemic symptoms.
  • Caterpillar-induced bleeding syndrome: Caterpillars from the Lonomia genus have spines along their body which can penetrate human skin and cause blood coagulation problems. The severity of the symptoms vary depending on the degree of envenomation but serious cases can result in death.
  • Caterpillar-induced bleeding syndrome -- Lonomia achelous: Lonomia achelous caterpillars are native to Northern Brazil and Venezuela. They have spines along their body which can penetrate human skin and cause blood coagulation problems. The severity of the symptoms vary depending on the degree of envenomation but serious cases can result in death.
  • Caterpillar-induced bleeding syndrome -- Lonomia obliqua: Lonomia obliqua caterpillars are native to Southern Brazil and have spines along their body which can penetrate human skin and cause blood coagulation problems. The severity of the symptoms vary depending on the degree of envenomation but serious cases can result in death.
  • Catheter infection: Infection due to an inserted catheter
  • Cathinone poisoning: Cathinone comes from the leaves of the Khat plant which is native to eastern Africa. Cathinone is a stimulant as well as have pain killing, weight loss and neuromuscular effects. The psychoactive effects are usually utilized by chewing on the leaves of the plant but sometimes dried leaves are used.
  • Cauda equina syndrome: Is a neurological syndrome which occurs when a vertebral disc protrudes and compresses the spinal cord.
  • Caudal appendage -- deafness: A very rare syndrome characterized mainly by deafness, finger bone abnormalities and a spinal extension giving a tail-like appearance (caudal appendage).
  • Celery urine odor in children: Celery urine odor in children is a condition in which the urine has an abnormal smell similar to the smell of celery.
  • Celiac Disease: Digestive intolerance to gluten in the diet.
  • Cephalothoracic progressive lipodystrophy: A rare acquired disorder that involves adipose tissue abnormalities and is characterized by loss of adipose tissue mainly in the trunk and arms.
  • Cerebro-oculo-nasal syndrome: A rare syndrome characterized mainly by eye, nose and brain malformations.
  • Cervical cancer: A condition which is characterized by the occurrence of malignancy on the cervix
  • Cervical dilatation: Cervical dilatation is the opening of the cervix, the entrance to a woman's uterus.
  • Cervical dilation: Dilation of the cevix.
  • Cervical erosion: A shallow superficial ulceration of the cervix.
  • Cervical polyps: Benign polyps on the cervix of the uterus
  • Cervical ribs, sprengel anomaly, anal atresia, urethral obstruction: A rare disorder characterized mainly by kidney and urinary system abnormalities, scoliosis and omphalocele. The features of the disorder are variable with male cases tending to be more severe than female cases. Only a few cases of this condition have been reported.
  • Cervicitis: A condition which is characterized by inflammation of the cervix
  • Cervix bleeding: Inflammatory conditions which cause cervical bleeding
  • Cervix blister: Inflammatory conditions which cause cervical blisters
  • Cervix bruise: Inflammatory conditions which cause cervical pain
  • Cervix burning sensation: Inflammatory conditions which cause burning sensation of the cervix
  • Cervix conditions: Conditions of the cervix (entrance) of the female uterus.
  • Cervix deformity: Inflammatory conditions which cause cervical pain
  • Cervix infection: Inflammatory conditions of the cervix.
  • Cervix inflammation: Inflammatory conditions of the cervix.
  • Cervix itch: Inflammatory conditions which cause cervical pain
  • Cervix lump: Inflammatory conditions which cause cervical lump
  • Cervix obstruction: Obstruction either at the internal or external os.
  • Cervix pain: Inflammatory conditions which cause cervical pain
  • Cervix rash: Inflammatory conditions which cause cervical rash and erythema
  • Cervix redness: Inflammatory conditions of the cervix which causes erythema.
  • Cervix spasm: Inflammatory conditions which cause cervical spasms
  • Cervix swelling: Inflammatory conditions which cause cervical swelling
  • Cervix symptoms: Symptoms affecting the cervix
  • Cervix ulcer: Inflammatory conditions which cause cervical ulcers
  • Cervix weakness: Weakness of the cervical muscle contraction.
  • Chancre: An ulcer like eruption that is located on an epithelial surface
  • Chancroid: An sexually transmitted disease caused by the Haemophilus ducreyi bacteria and is characterized by painful genital ulceration.
  • Change in sexual desire in pregnancy: Change in sexual desire in pregnancy is an alteration in a woman's libido during pregnancy. Libido may be increased or decreased, and can very at different times throughout the pregnancy.
  • Changes in normal menstrual cycle: can cause increase or decrease in the menstrual flow
  • Changes in sexual desire: Changes that occur in ones sexual desires
  • Cheesy vaginal discharge: curdy white precipitate which bleeds on removal
  • 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 -- 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 -- 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 -- 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 -- 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 -- 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 -- Anticoagulant rodenticide: Anticoagulant rodenticide is a chemical used to control rodents. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- 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 -- 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 -- 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 -- 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 -- Benzidine: Benzidine is a chemical used mainly in the production of azo dyes for such products as leather, paper and textiles. 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 -- Boric Acid: Boric Acid is a chemical used mainly in foods (preservative, emulsifier, neutralizer), antiseptics, pesticides and contact lens cleaners. Ingestion and other exposures to the chemical can cause various symptoms. Application of boric acid directly to damaged skin can cause the chemical to be absorbed rapidly into the body and lead to death. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Brodifacoum: Brodifacoum is a chemical used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Bromadiolone: Bromadiolone is a chemical used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- 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 -- 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 -- Chlorate salts: Chlorate salt is a chemical used mainly in herbicides and in the manufacture of matches and explosives. 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 -- 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 -- Chloromethane: Chloromethane is a chemical used mainly in the production of silicones as well as agricultural chemicals, butyl rubber and other products. 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 -- Clinitest tablet: Clinitest tablet are used to test sugar levels in urine. The tablets contain various chemicals (copper sulfate, sodium hydroxide, sodium carbonate) and eating them can cause serious symptoms. The chemicals cause damage to the gastrointestinal lining and the damage may continue for weeks after the poison was ingested. Death can result in severe cases. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Cresols: Cresols are a group of chemicals that occur naturally in mammals and various plants. It is also manufactured and used in the production of disinfectants, deodorizers and pesticides. 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 -- Cresylic acid: Cresylic acids are a group of chemicals that are used as solvents and in the manufacture of various products such as deodorants, disinfectants, pesticides, glues, paints, herbicides, pharmaceuticals as well as others. 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 -- Cypermethrin: Cypermethrin is a widely used 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.
  • Chemical poisoning -- Demeton-S-methyl: Demeton-S-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 -- Diazinon: Diazinon 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 -- Dichlorvos: Dichlorvos 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 -- Dicrotophos: Dicrotophos is a toxic 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 -- Dieldrin: Dieldrin is a chemical used mainly to prevent termite infestations. Ingestion and other exposures to the chemical can cause various symptoms. This chemical may be absorbed readily 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 -- Dioxathion: Dioxathion 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 -- Disulfoton: Disulfoton 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 -- Ethion: Ethion 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 -- Ethylene Glycol: Ethylene Glycol is a chemical used mainly in antifreeze, coolants and as a solvent. 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. Symptoms tend to occur in three phases: the first 12 hours involves inebriation, seizuresand brain swelling; the second and third day involves deterioration of lung and heart function and the third stage involves kidney damage and possibly failure. Death can occur during any of the stages.
  • Chemical poisoning -- Fensulfothion: Fensulfothion 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 -- Fenthion: Fenthion is a chemical pesticide used as an insecticide and avicide. 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 -- Gasoline: Gasoline is a chemical used as a fuel for combustion engines. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Glyphosate: Glyphosate is a chemical used mainly in herbicides. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Hair Bleach: Hair bleach contain chemicals which can cause serious symptoms if ingested. The chemicals in the hair bleach can continue to cause gastrointestinal damage for weeks after ingestion. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Hair Dye: Hair dyes contain chemicals which can cause serious symptoms if ingested. The chemicals in the hair dye can continue to cause damage for weeks after ingestion. Some dyes contain lead or mercury which can cause neurological problems even if low level exposure occurs over an extended period of time. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Lead-containing Paint: Lead pain contains lead as well as other harmful chemicals. The lead in the pain is toxic (especially to young children) and ingesting fresh or old paint can cause serious symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Malathion: Malathion 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 -- Manganese: Manganese is a chemical used mainly in fertilizers, welding rods, matches, electrical coils, ceramics and animal food additives. 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 -- Methidathion: Methidathion is a chemical insecticide. 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 -- Methiocarb: Methiocarb is a toxic pesticide. 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 -- Methomyl: Methomyl 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 -- Monocrotophos: Monocrotophos is a chemical insecticide. 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 -- Monosodium Methanarsenate: Monosodium Methanarsenate is a chemical used mainly as a herbicide or pesticide. 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 -- Mouth Wash: Mouth wash contains various chemicals which can cause serious symptoms if sufficient quantities are swallowed. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Naphthalene: Naphthalene is a chemical used mainly as a moth repellant, toilet deodorizer and the manufacture of other chemicals. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Nitrates: Nitrates are chemicals used mainly in explosives and ammunitions but are also an ingredient in cold packs. 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: Sexual symptoms:

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

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Conditions listing medical complications: Sexual symptoms:

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

 

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