Assessment
Questionnaire

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

Glossary for Anal symptoms

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

  • 2q deletion: A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • AIDS-Related Opportunistic Infections: A term given to HIV patients who have a low CD4 count (below 200) which means that they have low levels of a type of immune cell called T-cells. AIDS patients tend to develop opportunistic infections and cancers. Opportunistic infections are infections that would not normally affect a person with a healthy immune system. The HIV virus is a virus that attacks the body's immune system.
  • 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 Neoplasms: A tumor that occurs in the abdomen.
  • Abdominal conditions: Medical conditions affecting the abdominal region.
  • Abdominal symptoms: Symptoms affecting the abdomen or digestive tract
  • Abnormal scintigraphy: A water perfused catheter measures anorectal pressures to assess voluntary and involuntary sphincter squeeze pressures
  • Absent anal opening: Absent anal opening is an abnormal condition in which there is no orifice or opening to create an anus at the end of the digestive tract.
  • Accessory navicular bone: An abnormal bone that develops in the arch in the middle of the foot. Often there are no symptoms but if the bone is large it may rub against shoes and cause problems.
  • Achlorhydria: Condition where there is no hydrochloric acid in the gastric juice
  • Acinic cell carcinoma: A usually slow-growing malignant tumor that that can occur in various parts of the body but is most often found in the pancreas, salivary glands, palate and upper lip. Symptoms are determined by the size and location of the growth.
  • Acute appendicitis: Infection of the appendix
  • Acute gastritis: Acute gastritis is the sudden onset of irritation or inflammation of the stomach.
  • Adenocarcinoid tumor: A rare type of tumor that occurs in the gastrointestinal tract and tends to metastasize. The symptoms are determined by the location of the tumors.
  • Adenomatous Polyposis of the Colon, autosomal dominant: A genetic condition characterized by the development of adenomatous polyps mainly in the colon and rectum. There may be hundreds or thousands of polyps and these polyps have a predisposition for becoming cancerous. The condition is inherited in an autosomal dominant manner and occurs in a familial pattern. Most patients have at least one parent with the condition.
  • Agranulocytosis: Extremely low level of white blood cells (basophils, eosinophils and neutrophils).
  • Alternating Bowel Habit IBS: It is a functional bowel disorder characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any organic cause. IBS may be associated with pain disorders.
  • Amebiasis: Intestinal inflammation caused by Entamoeba histolytica and often marked by symptoms such as frequent, loose bowel movements that contain blood and mucus. Also called intestinal amebic dysentery.
  • Amebic dysentery: Intestinal inflammation caused by Entamoeba histolytica and often marked by symptoms such as frequent, loose bowel movements that contain blood and mucus. Also called intestinal amebiasis.
  • Amoebiasis: An infectious disease caused by a free-living amoebic parasite called Entamoeba histolytica. The organism infects the bowel and causes gastroenteritis. Infection occurs through ingesting contaminated food or water. It is more common in countries with poor sanitation. The incubation period may last from days to weeks before symptoms appear.
  • Amyloidosis, familial cutaneous: Amyloidosis involves the abnormal deposit of a substance called amyloid in various parts of the body. The familial cutaneous form is characterized by brown skin pigmentation as well as systemic symptoms such as failure to thrive, developmental delay, gastrointestinal problems and pneumonia.
  • Anal bleeding: The loss of blood per rectum
  • Anal bruise: A haematoma that occurs on the anus.
  • Anal cancer: A cancerous malignancy that is located anatomically in the anus
  • Anal conditions: Conditions that affect the anus
  • Anal discomfort: A sensation of discomfort that is located in the region of the anus
  • Anal discomfort in pregnancy: Anal discomfort in pregnancy is pain or itch in the region of the anus. This may be accompanied by bleeding, a lump or discharge.
  • Anal disorder: diseases of the anal region
  • Anal disorder in pregnancy: Anal disorder in pregnancy includes pain or itch in the region of the anus. This may be accompanied by bleeding, a lump or discharge.
  • Anal disorders in adults:
  • Anal fissure: A painful ulcer linear to the margin of the anus
  • Anal fissure in children:
  • Anal hematoma: Anal hematoma is a collection of blood that has leaked from blood vessels in the anus.
  • Anal itching: Itching near or around the anus
  • Anal lump: Lump in the anal area as a symptom
  • Anal lump in children: An anal lump in children includes any lump, bump or mass in anus or immediate anal area in a child.
  • Anal lump in pregnancy: Anal lump in pregnancy may be accompanied by pain, itch, bleeding or discharge.
  • Anal pain: A sensation of pain that is located in the region of the anus
  • Anal pain in pregnancy: Anal pain in pregnancy be accompanied by bleeding, a lump or discharge.
  • Anal rash: An eruption on the skin of the anus.
  • Anal swelling: Swelling near or around the anus
  • Anal swelling in pregnancy: Anal swelling in pregnancy may be accompanied by pain, itch, bleeding or discharge.
  • Anal symptoms: Symptoms affecting the anus.
  • Anal symptoms in pregnancy: Anal symptoms in pregnancy include pain or itch in the region of the anus. This may be accompanied by bleeding, a lump or discharge.
  • Anal triangle blister: Raised small fluid filled lesion seen in the anal triangle.
  • Anal triangle bruise: Usually occurs due to trauma.
  • Anal triangle deformity: Distortion or malformation in the rectal and anal appearance.
  • Anal triangle infection: Usually occurs due to infection of the rectum and anus.
  • Anal triangle inflammation: Usually occurs due to infection of the rectum and the anus.
  • Anal triangle itch: Unpleasant sensation in the anal area.
  • Anal triangle obstruction: Obstruction of the rectal lumen and the anal opening.
  • Anal triangle rash: Raised erythematous lesion seen in the anal area.
  • Anal triangle redness: Usually occurs due to infection of the rectum and the anus.
  • Anal triangle swelling: Usually occurs due to infection of the rectum and the anus.
  • Anal triangle ulcer: Discontinuity in the lining mucosal layer of the anus.
  • Anal triangle weakness: weakness of the rectal and anal musculature.
  • Anal ulcer: The occurrence of an ulcer that is located in the anatomical location of the anus
  • Anogenital pruritus: An itching located in the anal and genital regions
  • Anorectal Malformations: Any condition which is a malformation of the normal anatomical design of the anorectum
  • Anorectal abscess: collection of pus in the anorectal region
  • Anorectal atresia: Congenital malformation where the anal or rectal opening is obstructed. The malformation is often associated with other abnormalities.
  • Anorectal disorders: Conditions that affect the anorectum
  • Anorectal manometry abnormal: A water perfused catheter measures anorectal pressures to assess voluntary and involuntary sphincter squeeze pressures
  • Anorectal pain: Pain in the anus or rectum regions
  • Anorectal pain in children: Anorectal pain in children is a pain or discomfort in the anal and/or rectal area.
  • Anorectal stricture: Narrowing of the anorectal canal.
  • Aplastic anemia: A blood disorder where the bone marrow produces insufficient new blood cells.
  • 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.
  • Asiatic porpoise poisoning: The Asiatic porpoise is eaten mainly in China. Eating the liver, internal organs and muscle tissue of the Asiatic porpoise can cause poisoning symptoms in humans if sufficient quantities are consumed. The nature of the toxin is unknown but it is believed that some cases result from very high levels of vitamin A in the liver.
  • Attenuated familial polyposis: A genetic condition characterized by the development of adenomatous polyps mainly in the colon and rectum. There may be hundreds or thousands of polyps and these polyps have a predisposition for becoming cancerous. The attenuated form of the condition is distinguished by the development of polyps in old age rather than during the first decades of life.
  • 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.
  • Autosomal Recessive Polycystic Kidney Disease: Severe form of PKD, a genetic kidney disease.
  • Autosomal Recessive Tetra-Amelia: A rare disorder characterized by the absence of all four extremities as well as skeletal, nervous system, craniofacial and other abnormalities. The condition is causes death before or soon after birth.
  • 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.
  • Bannayan-Zonana syndrome: A rare genetic disorder characterized by macrocephaly, intestinal polyposis, pigmentation of penis and benign tumor-like growths.
  • Banti Syndrome: A rare conditions where chronic congestive spleen enlargement causes it to destroy red blood cells too early. The spleen becomes enlarged due to an obstruction of blood flow in the organ and the resulting increase in blood pressure.
  • Banti's syndrome: A chronic, progressive condition marked by enlargement of the spleen which is associated with anemia, splenomegaly, ascites, jaundice, leucopenia, thrombocytopenia and gastrointestinal bleeding.
  • Ben-Ari-Shuper-Mimouni syndrome: A very rare syndrome characterized mainly by abnormal development of the structure separating the two halves of the brain as well as duplicated ureters that collect the urine from the kidney and deliver it to the bladder.
  • Biliary conditions: Medical conditions affecting the biliary system (liver, bile ducts, gallbladder, etc.) in digestion.
  • Blastocystis hominis: Common parasitic condition often causing digestive symptoms.
  • Bloody diarrhea: Diarrhea with blood in stool
  • Bloody stool: Blood appearing in the stool.
  • Bowel conditions: Medical conditions that affect the bowels
  • Bowel obstruction: A condition which is characterized by the obstruction of the gastrointestinal system
  • Bowel problems: Symptoms affecting the bowel
  • Brainerd diarrhea: Diarrheal condition of unknown cause.
  • Bright red blood on toilet paper:
  • Brodie pile: Inflammation of the mucous layer at the lower end of an anal fissure.
  • Bushmaster poisoning: The Bushmaster is a poisonous snake found in America.
  • Carbamate insecticide poisoning: Excessive ingestion of carbamate insecticide drugs.
  • 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.
  • Celiac Disease: Digestive intolerance to gluten in the diet.
  • Celiac disease, susceptibility to 1: The susceptibility to developing celiac disease due to a genetic defect on chromosome 6p21.3. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 10: The susceptibility to developing celiac disease due to a genetic defect on chromosome 3q25-q26. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 11: The susceptibility to developing celiac disease due to a genetic defect on chromosome 3q28. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 12: The susceptibility to developing celiac disease due to a genetic defect on chromosome 6q25.3. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 13: The susceptibility to developing celiac disease due to a genetic defect in the SH2B3 gene on chromosome 12q24. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 2: The susceptibility to developing celiac disease due to a genetic defect on chromosome 5q31-q33. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 3: The susceptibility to developing celiac disease due to a genetic defect on chromosome 2q33. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 4: The susceptibility to developing celiac disease due to a genetic defect on chromosome 19p13.1. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 5: The susceptibility to developing celiac disease due to a genetic defect on chromosome 15q11-q13. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 6: The susceptibility to developing celiac disease due to a genetic defect on chromosome 4q27. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 7: The susceptibility to developing celiac disease due to a genetic defect on chromosome 1q31. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 8: The susceptibility to developing celiac disease due to a genetic defect on chromosome 2q11-q12. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Celiac disease, susceptibility to 9: The susceptibility to developing celiac disease due to a genetic defect on chromosome 3p21. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
  • Cellulitis: inflammation of the subcutaneous fat
  • Cervical cancer: A condition which is characterized by the occurrence of malignancy on the cervix
  • Chancroid: An sexually transmitted disease caused by the Haemophilus ducreyi bacteria and is characterized by painful genital ulceration.
  • Chemical poisoning -- Anti-rust products: Anti-rust products contain various chemicals which are toxic if ingested. The ingested chemicals can continue to cause damage to the organs and gastrointestinal lining for weeks after the ingestion and severe cases can result in death. 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 -- Asphalt: Asphalt is the substance used in road surfacing and is also used in electrical adhesive and paints. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Automatic dishwashing detergent: Automatic dishwashing detergents contain chemicals which can cause severe symptoms if ingested. The chemicals in the dishwashing detergent 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 -- 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 -- Caulking products: Caulking products (e.g. silicon, acrylic, neoprene) are used to seal gaps and the chemicals in them 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 -- Chlorine: Chlorine is a chemical used mainly in bleaches, water disinfectants and in pulp mills. Ingestion and other exposures to the chemical can cause various symptoms. Chlorine is very corrosive and extensive damage to body tissues can result. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Cloth Dyes: Cloth dyes contain chemicals which are considered not toxic but the ingestion of large amounts cay cause symptoms. Some dyes contain corrosive ingredients which can cause severe gastrointestinal damage and even death in severe cases. Most household cloth dyes don't contain corrosive chemicals. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Diesel oil: Diesel oil is a commonly used fuel. Ingestion is unlikely due to the foul taste and smell. Accidental or purposeful ingestion can result in internal burns and various other symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Drain Cleaners: Drain cleaners contain chemicals which can cause severe symptoms if ingested. The chemicals in the drain cleaners 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 -- Drainpipe Cleaners: Drainpipe Cleaners contain chemicals which can cause severe symptoms if ingested. The chemicals in the drainpipe cleaners 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 -- Dye remover: Dye removers can contain chemicals which are corrosive and can cause severe gastrointestinal damage and even death in severe cases. The damage may continue for a few weeks after ingestion so death can occur weeks after the incident. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Emulsion paints: Emulsion paints (latex or water-based) contain 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 -- Furniture polish: Furniture polish contains chemicals (hydrocarbons) which can cause serious symptoms if ingested. The ingested chemicals can continue to cause damage to the organs and gastrointestinal lining for weeks after the ingestion and severe cases can result in death. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Jewelry cleaner: Jewelry cleaner contains various chemicals which can cause serious symptoms if ingested or other types of exposure occurs. 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 -- Lacquer: Lacquer contains various chemicals which can cause serious symptoms if ingested or other types of exposure occurs. 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 -- Lighter fluid: Lighter fluid contains various chemicals which can cause serious symptoms if ingested or other types of exposure occurs. 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 -- Metal cleaner: Metal cleaner contains various chemicals which can cause severe symptoms if ingested or other forms of exposure occur. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Metal polish: Metal polish contains various chemicals which can cause severe symptoms if ingested or other forms of exposure occur. 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 -- Mould remover: Mould removers contains various chemicals which can cause serious symptoms if swallowed, inhaled or skin and eye exposure occurs. 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 -- Oven Cleaners: Oven cleaners contain toxic chemicals which can cause serious symptoms on exposure. Severe gastrointestinal burns can be caused by ingesting oven cleaner. The burns can lead to perforation which involves a high risk of death. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Pool Cleaners: Pool Cleaners contain various chemicals (mainly chlorine) which can cause serious symptoms if sufficient quantities are swallowed. The chemicals are very damaging to the mucosal linings in the body. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chemical poisoning -- Tar remover: Tar remover contains various chemicals (mainly hydrocarbons) 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 -- White Phosphorus: White Phosphorus is a chemical used mainly in fertilizers, water treatment, rodenticides and insecticides (for cockroaches). 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 -- Window cleaner: Window cleaner contains various chemicals (usually alcohols and ammonia) which can cause serious symptoms if sufficient quantities are ingested. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chilaiditi syndrome: A rare disorder where a part of the colon, or sometimes intestine, is abnormally positioned between the liver and the diaphragm. The defect may occur in people who have chronic lung disease or abdominal ascites but may also occur in healthy individuals without causing symptoms.
  • Chlamydia: Common sexually transmitted disease often without symptoms.
  • Chlamydial infection: Infection from Chlamydia genus.
  • Chlorophacinone rodenticide poisoning: Chlorophacinone is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Cholangitis: bile duct inflammation (cholangitis)
  • Cholecystitis: inflammation of the gall bladder.
  • Chromosome 10p terminal deletion syndrome: A very rare syndrome caused by a chromosomal defect (10p terminal deletion) and can result in a variety of malformations that are similar to DiGeorge syndrome and velocardiofacial syndrome.
  • Chromosome 12, Isochromosome 12p Mosaic: A very rare disorder genetic disorder involving abnormalities in chromosome 12. The severity of symptoms is variable and tends to include a wide range of defects and abnormalities.
  • Chromosome 12p tetrasomy syndrome: A rare chromosomal disorder where there are four copies of the short arm (p) of chromosome 12 rather than the normal two resulting in various abnormalities.
  • Chromosome 2, monosomy 2q: A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Chromosome 22q11 Deletion Spectrum: A rare chromosomal disorder where a small piece of genetic material is missing from chromosome 22 at the q11 location.
  • Chromosomes 1 and 2, monosomy 2q duplication 1p: A very rare chromosomal disorder where a portion of chromosome 2q shifts to chromosome 1p resulting in duplication of chromosome 1p and deletion of chromosome 2q. The defect results in various abnormalities including retarded fetal growth, small head and skeletal and facial defects.
  • Chronic Granulomatous Disease: A very rare inherited blood disorder where certain cells involved with immunity (phagocytes) are unable to destroy bacteria and hence the patient suffers repeated bacterial infections.
  • Chronic Pesticide poisoning -- xylene: Xylene is an ingredient used in certain insecticides. Exposure to the chemical can cause a range of symptoms depending on the level and route of exposure. Exposure can occur through inhalation, ingestion, the skin or eyes. Acute exposure involves a exposure over a short period of time whereas chronic exposure occurs over a longer period of time.
  • Chronic inflammatory diarrhea: Inflammatory diarrhea occurs when there is damage to the mucosal lining or brush border, which leads to a passive loss of protein-rich fluids, and a decreased ability to absorb these lost fluids.
  • Clostridium perfringens food poisoning: Common type of food poisoning.
  • Colitis: Inflammation of the colon
  • Colitis like hematochezia: Disorders which can cause rectal bleeding( hematochezia) similar to that in case of colitis.
  • Collagenous celiac disease: Collagenous celiac disease is used to describe progressive celiac disease characterized by the presence of a layer of collagen (scarring) in the intestinal layers. This form of celiac disease usually fails to respond to treatments such as gluten-free diets. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The condition usually fails to respond to treatment and has a poor prognosis.
  • Colon Cancer, Familial: A genetic condition characterized by the development of adenomatous polyps mainly in the colon and rectum. There may be hundreds or thousands of polyps and these polyps have a predisposition for becoming cancerous.
  • Colon conditions: Any condition affecting the colon
  • Colonic Inertia: The nerves and muscles of the bowel do not function normally resulting in chronic constipation.
  • Colonic diverticulosis: Diverticulosis, otherwise known as "diverticular disease", is the condition of having diverticula in the colon which are outpocketings of the colonic mucosa and submucosa through weaknesses of muscle layers in the colon wall.
  • Colorectal Cancer, Susceptibility to, 1: Colorectal cancer refers to cancer of the colon (bowel) or cancer of the rectum, depending on the region affected. It is an under-diagnosed condition because it has no early symptoms. Even when symptoms occur, both the symptoms and the diagnostic tests required are considered embarrassing by many, leading to delayed diagnosis. However, early diagnosis is crucial as colon cancer is a leading cause of death. There are various genes which are linked to an increased risk of developing colorectal cancer. Not all patients with the genetic defect will develop colorectal cancer but the presence of additional triggering factors such as alcohol may trigger the development in those genetically susceptible. Type 1 is linked to a defect on chromosome 9.
  • Colorectal Cancer, Susceptibility to, 10: Colorectal cancer refers to cancer of the colon (bowel) or cancer of the rectum, depending on the region affected. It is an under-diagnosed condition because it has no early symptoms. Even when symptoms occur, both the symptoms and the diagnostic tests required are considered embarrassing by many, leading to delayed diagnosis. However, early diagnosis is crucial as colon cancer is a leading cause of death. There are various genes which are linked to an increased risk of developing colorectal cancer. Not all patients with the genetic defect will develop colorectal cancer but the presence of additional triggering factors such as alcohol may trigger the development in those genetically susceptible. Type 10 is linked to a defect on chromosome 19q.
  • Colorectal Cancer, Susceptibility to, 11: Colorectal cancer refers to cancer of the colon (bowel) or cancer of the rectum, depending on the region affected. It is an under-diagnosed condition because it has no early symptoms. Even when symptoms occur, both the symptoms and the diagnostic tests required are considered embarrassing by many, leading to delayed diagnosis. However, early diagnosis is crucial as colon cancer is a leading cause of death. There are various genes which are linked to an increased risk of developing colorectal cancer. Not all patients with the genetic defect will develop colorectal cancer but the presence of additional triggering factors such as alcohol may trigger the development in those genetically susceptible. Type 11 is linked to a defect on chromosome 20p.
  • Colorectal Cancer, Susceptibility to, 2: Colorectal cancer refers to cancer of the colon (bowel) or cancer of the rectum, depending on the region affected. It is an under-diagnosed condition because it has no early symptoms. Even when symptoms occur, both the symptoms and the diagnostic tests required are considered embarrassing by many, leading to delayed diagnosis. However, early diagnosis is crucial as colon cancer is a leading cause of death. There are various genes which are linked to an increased risk of developing colorectal cancer. Not all patients with the genetic defect will develop colorectal cancer but the presence of additional triggering factors such as alcohol may trigger the development in those genetically susceptible. Type 2 is linked to a defect on chromosome 8q24.
  • Colorectal Cancer, Susceptibility to, 3: Colorectal cancer refers to cancer of the colon (bowel) or cancer of the rectum, depending on the region affected. It is an under-diagnosed condition because it has no early symptoms. Even when symptoms occur, both the symptoms and the diagnostic tests required are considered embarrassing by many, leading to delayed diagnosis. However, early diagnosis is crucial as colon cancer is a leading cause of death. There are various genes which are linked to an increased risk of developing colorectal cancer. Not all patients with the genetic defect will develop colorectal cancer but the presence of additional triggering factors such as alcohol may trigger the development in those genetically susceptible. Type 3 is linked to a defect on chromosome 16.
  • Colorectal Cancer, Susceptibility to, 4: Colorectal cancer refers to cancer of the colon (bowel) or cancer of the rectum, depending on the region affected. It is an under-diagnosed condition because it has no early symptoms. Even when symptoms occur, both the symptoms and the diagnostic tests required are considered embarrassing by many, leading to delayed diagnosis. However, early diagnosis is crucial as colon cancer is a leading cause of death. There are various genes which are linked to an increased risk of developing colorectal cancer. Not all patients with the genetic defect will develop colorectal cancer but the presence of additional triggering factors such as alcohol may trigger the development in those genetically susceptible. Type 4 is linked to a defect on chromosome 15.
  • Colorectal Cancer, Susceptibility to, 5: Colorectal cancer refers to cancer of the colon (bowel) or cancer of the rectum, depending on the region affected. It is an under-diagnosed condition because it has no early symptoms. Even when symptoms occur, both the symptoms and the diagnostic tests required are considered embarrassing by many, leading to delayed diagnosis. However, early diagnosis is crucial as colon cancer is a leading cause of death. There are various genes which are linked to an increased risk of developing colorectal cancer. Not all patients with the genetic defect will develop colorectal cancer but the presence of additional triggering factors such as alcohol may trigger the development in those genetically susceptible. Type 5 is linked to a defect on chromosome 10p14.
  • Colorectal Cancer, Susceptibility to, 6: Colorectal cancer refers to cancer of the colon (bowel) or cancer of the rectum, depending on the region affected. It is an under-diagnosed condition because it has no early symptoms. Even when symptoms occur, both the symptoms and the diagnostic tests required are considered embarrassing by many, leading to delayed diagnosis. However, early diagnosis is crucial as colon cancer is a leading cause of death. There are various genes which are linked to an increased risk of developing colorectal cancer. Not all patients with the genetic defect will develop colorectal cancer but the presence of additional triggering factors such as alcohol may trigger the development in those genetically susceptible. Type 6 is linked to a defect on chromosome 8q23.
  • Colorectal Cancer, Susceptibility to, 7: Colorectal cancer refers to cancer of the colon (bowel) or cancer of the rectum, depending on the region affected. It is an under-diagnosed condition because it has no early symptoms. Even when symptoms occur, both the symptoms and the diagnostic tests required are considered embarrassing by many, leading to delayed diagnosis. However, early diagnosis is crucial as colon cancer is a leading cause of death. There are various genes which are linked to an increased risk of developing colorectal cancer. Not all patients with the genetic defect will develop colorectal cancer but the presence of additional triggering factors such as alcohol may trigger the development in those genetically susceptible. Type 7 is linked to a defect on chromosome 11.
  • Colorectal Cancer, Susceptibility to, 8: Colorectal cancer refers to cancer of the colon (bowel) or cancer of the rectum, depending on the region affected. It is an under-diagnosed condition because it has no early symptoms. Even when symptoms occur, both the symptoms and the diagnostic tests required are considered embarrassing by many, leading to delayed diagnosis. However, early diagnosis is crucial as colon cancer is a leading cause of death. There are various genes which are linked to an increased risk of developing colorectal cancer. Not all patients with the genetic defect will develop colorectal cancer but the presence of additional triggering factors such as alcohol may trigger the development in those genetically susceptible. Type 8 is linked to a defect on chromosome 14q.
  • Colorectal Cancer, Susceptibility to, 9: Colorectal cancer refers to cancer of the colon (bowel) or cancer of the rectum, depending on the region affected. It is an under-diagnosed condition because it has no early symptoms. Even when symptoms occur, both the symptoms and the diagnostic tests required are considered embarrassing by many, leading to delayed diagnosis. However, early diagnosis is crucial as colon cancer is a leading cause of death. There are various genes which are linked to an increased risk of developing colorectal cancer. Not all patients with the genetic defect will develop colorectal cancer but the presence of additional triggering factors such as alcohol may trigger the development in those genetically susceptible. Type 9 is linked to a defect on chromosome 16q.
  • Colorectal Polyps: Polyp growths in the colon or rectum.
  • Colorectal adenomatous polyposis, dominant: A genetic condition characterized by the development of adenomatous polyps mainly in the colon and rectum. There may be hundreds or thousands of polyps and these polyps have a predisposition for becoming cancerous. The condition is inherited in an autosomal dominant manner and occurs in a familial pattern. Most patients have at least one parent with the condition.
  • Colorectal adenomatous polyposis, recessive: A genetic condition characterized by the development of adenomatous polyps mainly in the colon and rectum. There may be hundreds or thousands of polyps and these polyps have a predisposition for becoming cancerous.
  • Colorectal cancer: Cancer of the colon (bowel) or rectum.
  • Congenital aplastic anemia: A genetic disorder where the bone marrow does not produce enough blood cells. Fanconi's anemia is an example of congenital aplastic anemia.
  • Congenital lactase deficiency: A congenital metabolic disorder where a deficiency of an enzyme called lactase impairs the body's ability to digest milk and other products that contain lactose. Symptoms tend to occur soon after consuming such products. The severity of symptoms depends on the degree of lactase deficiency.
  • Congenital megacolon: A rare condition similar to Hirschsprung's disease where abnormalities in the bowel muscles prevent it from contracting normally and pushing the fecal matter through. Congenital megacolon differs from Hirschsprung's disease in that the whole colon tends to be dilated.
  • Congenital short bowel: A rare birth defect where the bowel is abnormally short. A short bowel can impair the body's ability to absorb enough nutrients and hence result in malabsorption.
  • Congenital sucrose-isomaltose malabsorption: A rare disorder where a congenital deficiency of an enzyme (sucrase-isomaltase) prevents the absorption of sucrase and isomaltose consumed in the diet.
  • Constant Anorectal pain: Constant anorectal pain is discomfort in the anal and/or rectal area that is steady.
  • Constipation: Hardness of stool or difficulty or inability to pass feces.
  • Constipation-predominant IBS: IBS is a functional bowel disorder characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits
  • Corpus callosum agenesis -- polysyndactyly: A rare syndrome characterized by skin and gastrointestinal defects, extra digits and skull and facial anomalies.
  • Corpus callosum agenesis double urinary collecting: A very rare syndrome characterized mainly by abnormal development of the structure separating the two halves of the brain as well as duplicated ureters that collect the urine from the kidney and deliver it to the bladder.
  • Corpus callosum agenesis double urinary collecting system and trigonocephaly: A very rare syndrome characterized mainly by abnormal development of the structure separating the two halves of the brain as well as duplicated ureters that collect the urine from the kidney and deliver it to the bladder.
  • Costello syndrome: A rare genetic disorder characterized by papillomas which may become malignant.
  • Coumachlor rodenticide poisoning: Coumachlor is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Coumafuryl rodenticide poisoning: Coumafuryl is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Coumatetralyl rodenticide poisoning: Coumatetralyl is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Craniosynostosis radial aplasia syndrome: A rare genetic disorder characterized by premature closing of skull bones, growth deficiency and anal, limb, urogenital and craniofacial abnormalities.
  • Crohn's disease: Crohn's disease causes inflammation of the digestive system. It is one of a group of diseases called inflammatory bowel disease. The disease can affect any area from the mouth to the anus. It often affects the lower part of the small intestine called the ileum.
  • Currarino triad: A rare birth malformation consisting of abnormalities in the anal, sacral and presacral areas.
  • Cycad nut poisoning: The cycad nut contains a toxic chemical called cyasin which can be leeched out by soaking in water. The nuts are often used as a food source but it is important to leech out the toxic chemicals first. Eating nuts that still contain the toxin can cause serious symptoms. Cycad nuts may also increase the risk of developing liver cancer.
  • Cyclosporiasis: A parasitic disease caused by Cyclospora cayetensis which is transmitted by ingestion of food or water contaminated by infected fecal matter. Some cases are asymptomatic while others can be quite severe and untreated cases can suffer relapses.
  • Cyclosporiosis: A parasitic disease caused by Cyclospora cayetensis which is transmitted by ingestion of food or water contaminated by infected fecal matter. Some cases are asymptomatic while others can be quite severe and untreated cases can suffer relapses.
  • Cystic Fibrosis: Cystic fibrosis is a hereditary disease affecting the exocrine (mucus) glands of the lungs, liver, pancreas, and intestines, causing progressive disability due to multisystem failure.
  • Decreased gastrointestinal motility: Decreased gastrointestinal motility is a lowered functioning of the gastrointestinal tract in which food is not digested and moved normally through the gastrointestinal tract.
  • Decreased intestinal motility: slowed peristalsis
  • Defibrination syndrome: The generation of fibrin in the blood and consumption of pro-coagulants and platelets occurring in complications of obstetrics
  • Del (2) (q22-q24.2): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in one reported case. The manifestations linked to most genetic defects are often variable to some degree.
  • Deletion 10pter: A very rare syndrome caused by a chromosomal defect (10p terminal deletion) and can result in a variety of malformations that are similar to DiGeorge syndrome and velocardiofacial syndrome.
  • Deletion 22q11: A rare chromosomal disorder where a small piece of genetic material is missing from chromosome 22 at the q11 location.
  • Deletion 2q: A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion.
  • Developmental Lactase Deficiency: This form of lactase deficiency occurs in premature infants. Lactase enzyme activity usually develops late in pregnancy so a preterm infant will not yet have developed this enzyme function. The greater the degree of prematurity, the greater the reduction in lactase activity.
  • Diaper rash: Red rash in diaper area of infants
  • Diarrhea: Loose, soft, or watery stool.
  • Diarrhea-predominant IBS: IBS is a functional bowel disorder characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits
  • Difenacoum rodenticide poisoning: Difenacoum is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Difethialone rodenticide poisoning: Difethialone is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Diffuse systemic sclerosi: A rare condition that characterized by skin tightness affecting the trunk and extremities as well as organ involvement. It involves an early period of internal inflammation which distinguishes it from other forms of scleroderma and the organ involvement can be severe and even life-threatening.
  • Digestive duplication: Duplication of a part of the digestive system. Duplication of the anal canal is the least common where as duplication of the Symptoms vary depending on what part of the digestive system is duplicated.
  • Digestive symptoms: Any symptoms affecting the digestive tract.
  • Digestive tract cancer:
  • Diphacinone rodenticide poisoning: Diphacinone is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Dipylidiasis: A parasitic intestinal infection caused by a tapeworm called Dipylidium caninum. The parasite commonly infects dogs and cats but can occur in humans. Transmission usually occurs through accidental ingestion of infected cat or dog fleas. Children are more likely to become infected and are also more likely to have symptoms.
  • Dipylidium: The dog tapeworm
  • Dipylidium caninum infection: A tapeworm (Dipylidium caninum) infection. Transmission can occur when infected animal fleas are accidentally ingested.
  • Distal colorectal cancer: Approximately 75% of colorectal cancers are sporadic and develop in people with no specific risk factors. The remaining 25% of cases occur in people with significant risk factors.
  • Diverticular Disease: Protrusions of the colon wall (diverticulosis) or their inflammation (diverticulitis)
  • Diverticular disease and diverticulitis:
  • Down's syndrome associated Celiac Disease: Patients with Down's syndrome have a high degree of susceptibility to developing celiac disease. Up to 17% of Down's syndrome sufferers develop celiac disease but this rate varies amongst age groups and country of origin. 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.
  • Duodenal conditions: Any condition that affects the duodenum
  • Duodenal ulcer due to antral G-cell hyperfunction: A rare disease where duodenal ulcers form due to the over-functioning antral G-cells. G-cells secrete gastrin which is a hormone that initiates gastric acid production in the stomach. Excessive stomach acid can lead to ulcers.
  • Duodenitis: Inflammation of the duodenal mucosa
  • Dup (1)(pter-p31) and del(2)(q33-qter): A very rare chromosomal disorder where a portion of the short arm (pter-p31) of chromosome one is duplicated and a portion of the long arm (q33-qter) of chromosome 2 is deleted. The reported patient died at 3 months of age.
  • Dup (2) (p23-p21): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in two reported cases. The manifestations linked to most genetic defects are often variable to some degree.
  • Durand-Nicolas-Favre syndrome: Infection by Chlamydia trachomatosis which can be contracted through sexual intercourse or through contact with contaminated material.
  • Dysentery: severe diarrhoea with passage of blood and mucus
  • Emanuel syndrome: A rare chromosomal disorder where a portion of chromosome 11 is translocated with a portion of chromosome 22. The disorder involves a wide range of abnormalities such as kidney, genital and heart abnormalities, mental retardation, small head and failure to thrive.
  • Endometriosis: Misplaced uterus tissue causing scar tissue.
  • Enteroaggregative E. Coli infection: A bacterial infection that results from ingesting contaminated food or water and results in diarrhea that tends to last for weeks. It most often causes diarrhea in children in developing countries. Enteroaggregative refers to the grouping nature of the bacterial attack on the intestinal lining.
  • Enterocolitis: Serious type of intestinal infection
  • Enterohemorrhagic E. Coli infection: A bacterial infection that results from ingesting contaminated food or water and results in bloody diarrhea. Enterohemorrhagic refers to the intestinal bleeding associated with the infection.
  • Enterohemorrhagic Escherichia Coli Infection: An Escherichia Coli infection that occurs in the bowel causing an enterohemorrhagic condition
  • Enteroinvasive E. Coli infection: A type of bacterial infection that results from ingesting contaminated food or water and results in gastroenteritis. Enteroinvasive refers to the invasion of bacteria into the gastrointestinal lining. It tends to occur as occasional outbreaks in developed countries and as endemic infections in developing countries.
  • Erythema multiforme: An allergic inflammatory skin disorder which has a variety of causes and results in skin and mucous membrane lesions that affect mainly the hands, forearms, feet, mouth nose and genitals.
  • Esophageal varices: Abnormally dilated blood vessels in the wall of the esophagus. The condition is asymptomatic unless the blood vessel bursts which can result in death.
  • Essential thrombocytosis -- same as essential thrombocythemia: A rare blood disorder where the blood contains too many platelets due to excessive megakaryocytes (platelet-producing cells). Platelets are essential for blood clotting but in essential thrombocythemia excessive platelets can cause the blood to form abnormal clots. If the platelets are defective as well then bleeding problems can occur. The severity of the condition is variable.
  • FG Syndrome: A rare genetic disorder characterized by anal abnormalities, reduced muscle tone and a prominent forehead.
  • FG syndrome 1: A rare inherited disorder characterized by anal abnormalities, reduced muscle tone and abnormal brain development. In type 1, the genetic defect is located on chromosome Xq12-q21.31.
  • FG syndrome 2: A rare inherited disorder characterized by anal abnormalities, reduced muscle tone and abnormal brain development. In type 2, the genetic defect is located on chromosome Xq28.
  • FG syndrome 3: A rare inherited disorder characterized by anal abnormalities, reduced muscle tone and abnormal brain development. In type 3, the genetic defect is located on chromosome Xp22.3.
  • FG syndrome 4: A rare inherited disorder characterized by anal abnormalities, reduced muscle tone and abnormal brain development. In type 4, the genetic defect is located on chromosome Xp11.4-p11.3.
  • FG syndrome 5: A rare inherited disorder characterized by anal abnormalities, reduced muscle tone and abnormal brain development. In type 5, the genetic defect is located on chromosome Xq22.3.
  • Familial Colorectal Cancer: An inherited disorder in which affected individuals have a higher-than-normal chance of developing colorectal cancer and certain other types of cancer, often before the age of 50.
  • Familial Intestinal Polyposis: A genetic condition characterized by the development of adenomatous polyps mainly in the colon and rectum. There may be hundreds or thousands of polyps and these polyps have a predisposition for becoming cancerous.
  • Familial Lactase Deficiency: A congenital metabolic disorder where normal amounts of lactase are produced but the lactase is defective and unable to digest milk and other products that contain lactose. Symptoms tend to occur soon after consuming such products.
  • Familial Multiple Polyposis: A genetic condition characterized by the development of adenomatous polyps mainly in the colon and rectum. There may be hundreds or thousands of polyps and these polyps have a predisposition for becoming cancerous.
  • Familial adenomatous polyposis, autosomal dominant: A genetic condition characterized by the development of adenomatous polyps mainly in the colon and rectum. There may be hundreds or thousands of polyps and these polyps have a predisposition for becoming cancerous. The condition is inherited in an autosomal dominant manner and occurs in a familial pattern. Most patients have at least one parent with the condition.
  • Familial polyposis: Rare genetic disease causing multiple colorectal polyps
  • Familial polyposis -- classical: An inherited condition where polyps develop in the lining of the gastrointestinal tract. The polyps are initially benign but may become malignant if untreated.
  • Familial polyposis, autosomal recessive: An inherited condition where polyps develop in the lining of the gastrointestinal tract. The polyps are initially benign but may become malignant if untreated. The autosomal recessive form of this condition is characterized by fewer polyps than in other forms (less than 100) and is due to mutations in a different gene.
  • Febrile Seizures: Fever-caused seizures in infants or children.
  • Fecal incontinence: The loss of control of a persons bowel motions
  • Fecal straining: Straining for a bowel movement
  • Fetal and neonatal alloimmune thrombocytopenia: A rare, potentially life-threatening disorder where the mother's blood platelets are incompatible with that of the fetus and the mother's antibodies cross the placenta and destroy fetal platelets.
  • Finale rodenticide poisoning: Finale is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Fissures: Any cleft or groove especially a deep fold in the cerebral cortex involving its entire thickness
  • Flatulence: Gas passed from the anus
  • Flatulence in children: Flatulence in children is also called passing gas in a child.
  • Flocoumafen rodenticide poisoning: Flocoumafen is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Focal dermal hypoplasia: A rare genetic disorder characterized by bone, skin, teeth and pigmentation abnormalities as well as asymmetry of the face, trunk and extremities.
  • Folgorat rodenticide poisoning: Folgorat is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Food Additive Adverse reaction -- MSG: An intolerance to MSG is an adverse reaction (not an immune response) by the body to a food additive called MSG which is used in a number of foods. The adverse reaction results from the body's inability to metabolize or deal with the food additive. The amount of the substance required to trigger the onset of symptoms and the nature and severity of symptoms may vary considerably between patients.
  • Food Additive Adverse reaction -- amines: An intolerance to amines is an adverse reaction (not an immune response) by the body to amines which are found naturally in foods such as bananas, pineapples, vegetables, red wine, citrus fruit and many other foods. The adverse reaction results from the body's inability to metabolize or deal with the substance. The amount of the substance required to trigger the onset of symptoms and the nature and severity of symptoms may vary considerably between patients.
  • Food Additive Adverse reaction -- citric acid intolerance: An intolerance to citric acid is an adverse reaction (not an immune response) by the body to citric acid or foods containing citric acid. Citric acid can be found naturally in foods but is also frequently used as an additive to various foods. The adverse reaction results from the body's inability to metabolize the food. The amount of citric acid required to trigger the onset of symptoms and the nature and severity of symptoms may vary considerably between patients.
  • Food Additive Adverse reaction -- food additives: An intolerance to food additives is an adverse reaction (not an immune response) by the body to food additives. The adverse reaction results from the body's inability to metabolize or deal with the food additive. The amount of the substance required to trigger the onset of symptoms and the nature and severity of symptoms may vary considerably between patients.
  • Food Additive Adverse reaction -- salicylate: An intolerance to salicylates is an adverse reaction (not an immune response) by the body to salicylates which is an ingredient in aspirin but is also found naturally in various fruit, vegetables, herbs and spices. The adverse reaction results from the body's inability to metabolize or deal with the salicylate. The amount of the substance required to trigger the onset of symptoms and the nature and severity of symptoms may vary considerably between patients.
  • Food Additive Adverse reaction -- sulfite: An intolerance to sulfites is an adverse reaction (not an immune response) by the body to sulfites which is often used as a preservative in a variety of foods and medications including meats, salads and dried fruits. The adverse reaction results from the body's inability to metabolize or deal with the sulfite. The amount of the substance required to trigger the onset of symptoms and the nature and severity of symptoms may vary considerably between patients.
  • Food allergies: a food allergy is an adverse immune response to a food protein
  • Food intolerances: Any inability to tolerate particular foods.
  • Food poisoning: Poisoning from a substance or microbe in food.
  • Gallstones: A condition where biliary calculi form in the gallbladder
  • Gas in children: Gas in children is the presence of flatulence in a child.
  • Gas with discharge: Gas with discharge is flatulence that occurs with a solid or gaseous discharge from the rectum.
  • Gas/bloat syndrome: Excessive production of gas in the gastrointestinal system which causes bloating. Causes can include gastrointestinal infection, excessive gulping of air, altered diet and malabsorption disorders.
  • Gastritis: gastritis is inflammation of the gastric mucosa of the stomach
  • Gastrointestinal Stromal Tumors: Cancer that develops from stroma cells in the wall of the gastrointestinal tract. The primary locations are the small intestine, esophagus and esophagus with symptoms being determined by the location, stage and size of the tumor.
  • Gastrointestinal bleeding: Bleeding in any part of the digestive tract
  • Gastrointestinal neoplasm: A growth or excessive proliferation of cells in the lining of the gastrointestinal tract which includes the esophagus, intestine, pharynx and stomach. The growth may be benign or malignant. The symptoms are determined by the size, location and stage of the tumor.
  • Gastrointestinal tumors: Any tumor of the gastrointestinal (digestive) system, including cancers and benign tumors.
  • Genital herpes: Sexually transmitted infection of the genital region.
  • Giardia: Contagious parasitic digestive infection
  • Glucose-galactose malabsorption: An inherited metabolic disorder where the small intestine is unable to absorb and transport glucose and galactose that is consumed in the diet due to a lack of intestinal monosaccharidase.
  • Gluten allergy: Gluten allergy is an adverse reaction by the body's immune system to gluten or foods containing gluten. The specific symptoms that can result can vary considerably amongst patients from a severe anaphylactic reaction to asthma, abdominal symptoms, eczema or headaches. Gluten allergy is similar to celiac disease - celiac disease only occurs in people with a genetic defect which predisposes them to the condition whereas gluten can occur in anyone but is more common in people who are also prone to other allergies.
  • Gonorrhea: Common sexually transmitted disease often without symptoms.
  • HELLP syndrome: A rare potentially fatal condition that occurs in pregnant women and is frequently associated with pre-eclampsia.
  • Haemorrhoids in pregnancy: Haemorrhoids in pregnancy refers to the appearance of enlarged veins around the anus and rectum in a woman who is pregnant
  • Hamartomatous colorectal cancer: The hamartomatous polyposis syndromes are a heterogeneous group of disorders that share an autosomal-dominant pattern of inheritance and are characterized by hamartomatous polyps of the gastrointestinal tract.
  • Havoc rodenticide poisoning: Havoc is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Helicobacter cinaedi infection: Helicobacter cinaedi is a food borne bacterial infection which may cause mild to severe gastroenteritis.
  • Helicobacter fenneliae infection: Helicobacter fenneliae is a food borne bacterial infection which may cause mild to severe gastroenteritis.
  • Helicobacter pylori bacteria: A bacteria that can infect the gastrointestinal system
  • Helminthiasis: Infection of the human body with a parasitic worm such as roundworms and pinworms. The worms usually only involve the intestinal tract but sometimes they may invade other organs. The type and severity of symptoms is determined by the type of worm and the part of the body infected.
  • Hemolytic uremic syndrome: A rare condition characterized by acute kidney failure, hemolytic anemia and thrombocytopenia (reduced blood platelet count). The condition is often caused by upper respiratory infections or infectious diarrhea.
  • Hemorrhagic proctocolitis: Inflammation of the rectum and colon that results in bleeding.
  • Hemorrhoids: A condition characterized by the prolapse of an anal cushion that may result in bleeding and pain
  • Henoch-Schonlein purpura: A form of vasculitis (blood vessel inflammation) that affects blood capillaries and affects mostly the skin, kidneys, joints and stomach.
  • Herbal Agent adverse reaction -- Ginkgo biloba: Ginkgo biloba can be used as a herbal agent to treat conditions such as tinnitus, brain trauma, vertigo, blood vessel diseases and any other problems which benefit from the blood vessel dilating action of the herbal agent. Ginkgo biloba can cause adverse reactions in some people.
  • Hereditary Polyposis Coli: A genetic condition characterized by the development of adenomatous polyps mainly in the colon and rectum. There may be hundreds or thousands of polyps and these polyps have a predisposition for becoming cancerous.
  • Hereditary colorectal cancer: Individuals affected with hereditary colorectal cancer inherit a mutation in one of several genes involved in DNA mismatch repair, including MSH2, MLH1, and PMS2. ras gene mutations have been detected in the stool of patients with colorectal cancer and may in the future be useful in early diagnosis.
  • Hereditary nonpolyposis colon cancer: A rare disorder characterized by the inherited predisposition to develop colorectal cancer as well as cancers in other locations, particularly near the bowel. Even though sufferers face an increased risk of various cancers it does not mean that they will actually develop the cancer.
  • Hiatal hernia: Hernia of the stomach through the diaphragm muscle.
  • Hip cancer: The presence of tumour growth in the bone of the hip, whether due to primary malignancies e.g. leukaemic or myeloma infiltration of the bone marrow, or due to secondary metastases from another site e.g. lung or breast; cancer affecting bone of hip likely to affect other bones e.g. vertebra, ribs
  • Hochenegg ulcer: A rare, firm type of rectal tumor which is ulcerated in the middle.
  • Hookworm: Worm spread through feces with poor sanitation.
  • Houlston-Ironton-Temple syndrome: A very rare syndrome characterized mainly by a forearm abnormaity, heart defect and an eye anomaly called blepharophimosis.
  • Human Papillomavirus: Very common sexually transmitted disease causing genital warts and associated with certain cancers.
  • Hymenolepiasis: A rare parasitic disease caused by a tapeworm called Hymenolepis nana or Hymenlepis dimunita. Infestation occurs through fecal contamination or by accidentally consuming insects that have eaten the parasitic eggs.
  • Hypobetalipoproteinemia: A medical term for low levels of apolipoprotein (LDL cholesterol) in the blood.
  • Hypomagnesemia primary: Low blood magnesium levels which is caused by the abnormal absorption and excretion of the mineral and can be caused by such things as kidney problems and intestinal malabsorption.
  • Imperforate anus: A congenital disorder where the anus is missing or located in the wrong position.
  • Impossible syndrome: A very rare syndrome (only one reported case) characterized a range of severe malformations, premature birth and stillbirth.
  • Indandione rodenticide poisoning: Indandione is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Indigestion: Imprecise term for various digestive complaints
  • Inflammatory Bowel Disease 1: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 1 is linked to 16q12.
  • Inflammatory Bowel Disease 10: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 10 is linked to 2q37.1.
  • Inflammatory Bowel Disease 11: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 11 is linked to 7q22.
  • Inflammatory Bowel Disease 12: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 12 is linked to 3p21.
  • Inflammatory Bowel Disease 13: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 13 is linked to 7q21.1.
  • Inflammatory Bowel Disease 14: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 14 is linked to 7q32.
  • Inflammatory Bowel Disease 15: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 15 is linked to 10q21.
  • Inflammatory Bowel Disease 16: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 16 is linked to 9q32.
  • Inflammatory Bowel Disease 17: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 17 is linked to 1p31.1.
  • Inflammatory Bowel Disease 18: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 8 is linked to 16p.
  • Inflammatory Bowel Disease 19: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 19 is linked to 5q33.1.
  • Inflammatory Bowel Disease 2: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 2 is linked to 12p13.2-q24.1.
  • Inflammatory Bowel Disease 20: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 20 is linked to 10q24.
  • Inflammatory Bowel Disease 21: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 21 is linked to 18p11.
  • Inflammatory Bowel Disease 22: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 22 is linked to 17q21.
  • Inflammatory Bowel Disease 23: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 23 is linked to 1q32.
  • Inflammatory Bowel Disease 24: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 24 is linked to 20q13.
  • Inflammatory Bowel Disease 25: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 25 is linked to 21q22.
  • Inflammatory Bowel Disease 26: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 26 is linked to 12q15.
  • Inflammatory Bowel Disease 27: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 27 is linked to 13p13.3.
  • Inflammatory Bowel Disease 3: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 3 is linked to 6p21.3.
  • Inflammatory Bowel Disease 4: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 4 is linked to 14q11-q12.
  • Inflammatory Bowel Disease 5: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 5 is linked to 5q31.
  • Inflammatory Bowel Disease 6: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 6 is linked to 19p13.
  • Inflammatory Bowel Disease 7: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 7 is linked to 1p36.
  • Inflammatory Bowel Disease 9: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable. Inflammatory Bowel Disease 9 is linked to 3p26.
  • Inflammatory bowel disease: Inflammatory bowel disease refers to digestive symptoms resulting from chronic bowel inflammation. Crohn's disease and ulcerative colitis are two of the main subtypes of the disease. Scientists have discovered an array of genetic mutations which can result in an increased susceptibility to inflammatory bowel disease. Not all people with the genetic anomaly will develop the condition but it can increase the risk especially if other environmental factors are also present. The severity of the disease that develops is variable.
  • Inherited Hemolytic-Uremic Syndrome: A condition which is characterized by thrombotic microangiography occurring with renal failure, hemolytic anemia and severe thrombocytopenia
  • Intermittent onset of anal fissure:
  • Internal bleeding: The loss of blood internally from the circulation
  • Intestinal Conditions: Conditions that affect the intestines
  • Intestinal Flu: Sudden onset, generally short-lived infection of the gastrointestinal tract; may be caused by viruses, bacteria or protozoa
  • Intestinal Pseudoobstruction in Adults: A condition characterized by the clinical presentation of obstruction of the intestines when there is no mechanical cause.
  • Intestinal obstruction: Any obstruction that occurs in the gastrointestinal system
  • Intestinal pseudo-obstruction: A digestive disorder where the intestines are unable to contract normally and push food through the digestive system. This results in symptoms similar to an obstruction and hence the name pseudo-obstruction. The walls of the affected gastrointestinal tract becomes thin and the muscles that control its motion start to degenerate.
  • Intussusception: intussusception is the sliding of one part of the intestine into another
  • Irritable bowel syndrome: A chronic non inflammatory disease with a psychophysiologic basis
  • Itchy anus in children: Itchy anus in children refers to a child who has a anus that feels itchy.
  • Itchy anus inn children:
  • Jadassohn-Lewandowsky syndrome: A rare, inherited disorder characterized by thickening of nails, white patches on mouth and anus(leukoplakia) and thickened hard skin on soles and palms.
  • Juvenile polyposis of infancy: A genetic inherited risk of developing gastrointestinal tumors. The condition is characterized by gastrointestinal polyps which have a high risk of eventually becoming malignant. The polyps can cause gastrointestinal symptoms even if they aren't malignant.
  • Juvenile polyposis syndrome, infantile form: A genetic inherited risk of developing gastrointestinal tumors. The condition is characterized by gastrointestinal polyps which have a high risk of eventually becoming malignant. The polyps can cause gastrointestinal symptoms even if they aren't malignant.
  • Keratosis palmoplantaris -- adenocarcinoma of the colon: A rare disorder characterized by cancer of the secretory lining of the colon as well as thickening of the skin on the palms and soles. The colon cancer tends to grow slowly.
  • Klerat rodenticide poisoning: Klerat is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Lactose intolerance: lactose intolerance is the inability to metabolize lactose, a sugar found in milk and other dairy products, because the required enzyme lactase is absent in the intestinal system or its availability is lowered
  • Leukocyte Adhesion Deficiency, Type I:
  • Leukocyte adhesion deficiency type 1: A rare inherited disorder characterized by abnormal neutrophil functioning which reduces the body's immunity. The abnormal neutrophils are unable to be transported to sites of infection due to their inability to adhere to certain blood vessel components which would normally lead them to the infection site. Infections may be life-threatening as the body is unable to destroy bacteria effectively. Type 1 LAD specifically involves a lack of receptor proteins on the neutrophil which prevents it from adhering.
  • Lichen sclerosis: Disease causing leathery or dry skin in genital areas.
  • Liver symptoms: Symptoms affecting the liver
  • Lower abdominal symptoms: Symptoms affecting the lower abdominal region.
  • Lymphoma, Mucosa-Associated Lymphoid Tissue: Malignancies that occur in the lymphoid tissue found in mucosal linings (MALT) e.g. gastrointestinal tract, skin and lungs. Symptoms may vary considerably depending on which organs are involved but usually the stomach is involved. A significant portion of patients suffering from MALTomas also have autoimmune diseases.
  • Lynch Syndrome 1:
  • Lynch syndrome I: A rare disorder characterized by the inherited predisposition to develop colorectal cancer which usually occurs at a younger age than non-inherited forms. Type I differs from Type II in that there is an increased risk of colorectal cancers but not necessarily other cancers.
  • Lynch syndrome II: A rare disorder characterized by the inherited predisposition to develop colorectal cancer in the colorectal which usually occurs at a younger age than non-inherited forms. Type II differs from type I in that there is an increased risk of cancers in various parts of the body as well as colorectal cancer.
  • Lynch syndrome type I: Lynch syndrome is a rare disorder.The estimated proportion of all Colorectal cancers that are caused by Lynch syndrome depends on how this syndrome is defined, with traditional definitions being based on family history and age of onset. It is also known as hereditary nonpolyposis colorectal cancer syndrome(HNPCC). The syndrome is classified as Type I in the absence of extracolonic cancers and Type II if these are present.
  • Lynch syndrome type II: Lynch syndrome is a rare disorder.The estimated proportion of all Colorectal cancers that are caused by Lynch syndrome depends on how this syndrome is defined, with traditional definitions being based on family history and age of onset. It is also known as hereditary nonpolyposis colorectal cancer syndrome(HNPCC). The syndrome is classified as Type I in the absence of extracolonic cancers and Type II if these are present.
  • MSI-H colorectal cancer: MSI sporadic colorectal cancers with a high level of MSI (MSI-H) form a well defined group with distinct clinicopathologic features characterized by an overall better long-term prognosis.
  • MSI-L colorectal cancer: Colorectal cancer is classified based on the microsatellite instability status and this is important for effective clinical management. MSI-L colorectal cancer is not clearly defined.
  • MSS colorectal cancer: Microsatellite analysis is commonly used initial screening tests for hereditary nonpolyposis colorectal cancer.
  • Matikus rodenticide poisoning: Matikus is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Microcephaly immunodeficiency lymphoreticuloma: A very rare syndrome characterized mainly by a small head, reduced immunity and increased risk of cancer. There are a wide range of other abnormalities and symptoms that can occur.
  • Microscopic collagenous colitis: Microscopic collagenous colitis refers to inflammation of the colon that is only visible when the colon's lining is examined under a microscope. The appearance of the inner colon lining in microscopic colitis is normal by visual inspection during colonoscopy or flexible sigmoidoscopy.
  • Microscopic lymphocytic colitis: Microscopic lymphocytic colitis refers to inflammation of the colon that is only visible when the colon's lining is examined under a microscope. The appearance of the inner colon lining in microscopic colitis is normal by visual inspection during colonoscopy or flexible sigmoidoscopy.
  • Microscopic ulcerative colitis: Microscopic ulcerative colitis refers to inflammation of the colon that is only visible when the colon's lining is examined under a microscope. The appearance of the inner colon lining in microscopic colitis is normal by visual inspection during colonoscopy or flexible sigmoidoscopy.
  • Mouser rodenticide poisoning: Mouser is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Mouth symptoms: Symptoms of the mouth or oral area.
  • NASH syndrome: A form of fatty liver where fat and fibrous tissue accumulate in the liver. Fatty liver is normally seen in alcoholic patients but in NASH syndrome, alcohol is not a factor. The condition may be generally asymptomatic or in some cases may lead to progressive scarring (cirrhosis) of the liver. The condition has a variable progression.
  • Necrotizing enterocolitis: A rare disease that is tends to occur in premature infants and involves inflammation and destruction of gastrointestinal tissue. It usually occurs within weeks of birth - often after the start of milk feeding. The condition can be extremely serious and even fatal.
  • Nerve symptoms: Symptoms affecting the nerves
  • Neurodermatitis: Lichen simplex chronicus refers to thickened itchy skin that results from persistently rubbing or scratching an area of skin.
  • Neurofibromatosis, familial intestinal: A rare type of familial tumor that arises from intestinal nerves.
  • Neutropenia: A reduced number of neutrophils in the blood.
  • Nijmegen Breakage Syndrome: A very rare syndrome characterized mainly by a small head, reduced immunity and increased risk of cancer. There are a wide range of other abnormalities and symptoms that can occur.
  • Non-Specific Urethritis: Urethral infection usually sexually transmitted
  • Nonpolyposis colorectal cancer, familial: A rare disorder characterized by the inherited predisposition to develop colorectal cancer. Even though sufferers face an increased risk of various cancers it does not mean that they will actually develop the cancer.
  • Omphalocele -- exstrophy -- imperforate anus: A very rare syndrome characterized mainly by the absence of an anal opening, spine defects and omphalocele (abdominal organ protruding from the belly button).
  • Organophosphate insecticide poisoning: Excessive ingestion of organophosphate insecticides. The type and severity of symptoms varies depending on the exact poison ingested and the quantity.
  • Ovarian carcinosarcoma: A type of ovarian cancer.
  • Ovarian epithelial cancer: Development of cancer in the tissue of the outer covering of the ovaries.
  • Pallister Killian Mosaic Syndrome: Pallister Killian Mosaic Syndrome is a very rare disorder genetic disorder involving abnormalities in chromosome 12. The severity of symptoms is variable and tends to include a wide range of defects and abnormalities.
  • Pallister Mosaic Syndrome Tetrasomy 12p: A very rare disorder genetic disorder involving abnormalities in chromosome 12. The severity of symptoms is variable and tends to include a wide range of defects and abnormalities.
  • Pallister-Hall Syndrome: A rare genetic disorder characterized by hypothalamic hamartoblastoma, hypopituitarism, imperforate anus and polydactyly.
  • Pallister-Killian Syndrome: A rare genetic disorder due to tetrasomy of the 12th chromosome
  • Pancreatic Acinar Cell Tumors: Pancreatic acinar cell tumors are a rare type of tumor that develops from acinar cells in the pancreas. Normal acinar cells secrete enzymes and hence acinar cells in the tumor will also usually secrete additional enzymes - mostly lipase. This type of tumor usually occurs in old age.
  • Pancytopenia: A term used to describe a lack of all of the different types of blood cells - red and white blood cells and blood platelets. Cancer, infections and toxins are some of the causes of pancytopenia. Symptoms depend on the severity of the deficiency.
  • Pelvic lipomatosis: A rare disorder where benign fatty growths develop in the pelvic area. Mainly occurs in obese, hypertensive, black males during old age. The main symptoms of the disorder tend to be related to compression of various genitourinary organs by the abnormal mass.
  • Peptic Ulcer: Ulcer on the lining of the stomach or duodenum
  • Peptic ulcer / duodenal ulcer:
  • Perianal discomfort: Perianal discomfort is any type of pain that occurs in the area around the anus.
  • Perianal lesions: lesions in the perianal region
  • Perianal lesions in pregnancy: Perianal lesions in pregnancy refers to lesions around the anus in a woman who is pregnant.
  • Perirectal abscess: A pus-filled cavity that develops in the anal opening. The inflammation can be caused by injury to the anal area which can lead to bacteria entering the anal skin. The injury may be related to such things as anal fissures, hemorrhoids.
  • Piles: Prolapse of blood vessels through the anal passage
  • Pindone rodenticide poisoning: Pindone is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Pinworm: Small, threadlike parasitic worms mainly in colon and rectum
  • Plexosarcoma: A rare type of tumor that occurs in the gastrointestinal tract and retroperitoneum.
  • Polyarteritis: A systemic inflammation of arteries, especially involving the kidneys and gut.
  • Polycystic kidney disease, infantile type: Severe form of polycystic kidney disease which is a genetic kidney disease. Symptoms develop very early in life and may even be present during the fetal stage.
  • Polyposis, Adenomatous Intestinal, autosomal dominant: A genetic condition characterized by the development of adenomatous polyps mainly in the colon and rectum. There may be hundreds or thousands of polyps and these polyps have a predisposition for becoming cancerous. The condition is inherited in an autosomal dominant manner and occurs in a familial pattern. Most patients have at least one parent with the condition.
  • Portal hypertension: Portal hypertension is a condition in which the blood pressure is abnormally high in the portal vein system, which carries blood from the digestive organs to the liver.
  • Portal thrombosis: Clotting or obstruction of blood flow along the veins from the intestines and spleen and into the liver. This causes blood to back up and results various problems such as enlarged spleen and abdominal pain. The obstruction can occur acutely (over a short space of time) or chronically (over a longer period of time).
  • Portal vein thrombosis: Clotting or obstruction of blood flow along the portal vein and into the liver. This causes blood to back up and results various problems such as enlarged spleen and abdominal pain. The obstruction can occur acutely (over a short space of time) or chronically (over a longer period of time). The portal vein collects blood from the intestines and spleen and carries it to the liver.
  • Post-infectious IBS: Post-infecttios IBS is a functional bowel disorder characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits following any infection affecting the body.
  • Pregnancy symptoms: Symptoms related to pregnancy.
  • Premenstrual dysphoric disorder: Premenstrual dysphoric disorder is a diagnosis used to indicate serious premenstrual distress with associated deterioration in functioning.
  • Proctalgia: Rectal or anal pain.
  • Proctitis: Inflammation which occurs in the rectum
  • Protozoan Conditions: Any condition caused by the infection of the human being by a protozoan organism
  • Protozoan infections: A condition which is characterized by an infection caused by protozoans
  • Proximal colorectal cancer: Approximately 75% of colorectal cancers are sporadic and develop in people with no specific risk factors. The remaining 25% of cases occur in people with significant risk factors.
  • Pruritis ani:
  • Pruritus ani: common condition which causes itching and irritation around the anus
  • Psychiatric disorders associated Celiac Disease: Patients with Psychiatric disorders 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.
  • Psyllium -- adverse effects: The use of psyllium as a diet supplement can cause adverse symptoms.
  • Pudendal nerve entrapment: A condition where a nerve in the pelvis (pudendal nerve) becomes trapped or compressed. The problem can arise due to such things as pregnancy, postsurgical scarring and trauma but may also occur due to a birth malformation. Bicycle riding can also result in the condition.
  • Rambaud-Galian syndrome: A very rare syndrome characterized by the progressive deposition of a substance called hyaline in blood vessels of the digestive tract and kidneys. Calcification of the brain is also present.
  • Rapid gastric emptying: Dumping of undigested food from the stomach into intestine.
  • Ratak Plus rodenticide poisoning: Ratak Plus is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Rectal abscess: Abscess in the rectal area
  • Rectal bleeding: Bleeding from the anus or rectum.
  • Rectal cancer: A growth or excessive proliferation of cells in the rectum which is the final portion of the digestive system before the anus. The growth may be benign or malignant.
  • Rectal conditions: Any condition that affects the rectum
  • Rectal discharge: The secretion of fluids (faecal, mucus, blood, pus) from the anus.
  • Rectal fistula:
  • Rectal infection: An infection of the rectum - bacteria are the usual pathogens.
  • Rectal itch: Unpleasant sensation in the rectal area.
  • Rectal lump: Lump in the inner rectum or rectal region
  • Rectal mass: A mass felt within the rectum on palpation.
  • Rectal pain: Pain occurring on or around the rectum
  • Rectal prolapse: A condition which occurs when there is a protrusion of the rectal mucous membrane through the anal passage
  • Rectal swelling: Usually occurs due to infection of the rectum.
  • Rectal tenesmus: The feeling of inadequate voiding and the constant need to empty the bowel.
  • Rectal ulceration: An ulcer that forms within the rectum.
  • Recto anal disorders: disorders of the rectum and anus
  • Rectosigmoid neoplasm: A tumor that originates in the upper rectal area or sigmoid colon. The tumor may be benign or cancerous.
  • Rectum symptoms: Symptoms affecting the rectum at the end of the digestive tract.
  • Refractory Celiac Disease: Refractory Celiac Disease is celiac disease that fails to respond to treatment which involves a gluten-free diet. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The condition is quite uncommon and often the resulting poor absorption of nutrients from the intestines leads to a poor prognosis.
  • Rib symptoms: Symptoms affecting the ribs
  • Rodend rodenticide poisoning: Rodend is used as a rodenticide. The chemical may be absorbed through the skin. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • SCID: Major failure of the immune system, usually genetic.
  • Sarcoma: Any cancer of the connective tissue.
  • Schistosomiasis: Parasitic fluke infection in developing countries
  • Schistosomiasis japonica: A trematode which causes schistosomiasis japonica
  • Schistosomiasis mansoni: A trematode which causes schistosomiasis mansoni
  • Secondary Lactase Deficiency: This form of lactase deficiency results from some sort of damage to the intestines either due to a disease or surgery. Some possible causes include untreated celiac disease, long-term use of antibiotics, giardiasis, carcinoid syndrome, HIV enteropathy, gastrectomy and intestinal resection. Lactase enzyme activity usually develops late in pregnancy so a preterm infant will not yet have developed this enzyme function. The greater the degree of prematurity, the greater the reduction in lactase activity.
  • Secondary syphilis: A condition which is characterized by fever, multiform skin eruptions, iritis, alopecia, mucous patches and severe pain in the head and joints
  • Sensations: Changes to sensations or the senses
  • Severe constipation:
  • Shigella boydii: A form of bacterium
  • Shigella boydii infection: Shigella boydii is a species of bacteria from the Shigella genus. Infection with this bacteria causes diarrhea. The severity of the disease is variable depending on the underlying health of the individual - the young and old tend to be more severely affected. Infection usually occurs through the fecal-oral route. Infection can be transmitted between people unless appropriate hygiene measures are undertaken. Some infected patients are asymptomatic and are those more likely to transmit infection to other people.
  • Shigella dysenteriae infection: Shigella dysenteriae is a species of bacteria from the Shigella genus. Dysenteriae is the most common cause of epidemic dysentery in condensed populations such as refugee camps. Infection with this bacteria causes diarrhea. The severity of the disease is variable depending on the underlying health of the individual - the young and old tend to be more severely affected. Infection usually occurs through the fecal-oral route. Infection can be transmitted between people unless appropriate hygiene measures are undertaken. Some infected patients are asymptomatic and are those more likely to transmit infection to other people.
  • Shigella flexneri: A form of bacterium
  • Shigella flexneri infection: Shigella flexneri is a species of bacteria from the Shigella genus. Flexneri is the most common cause of Shigellosis in the world. Infection with this bacteria causes diarrhea. The severity of the disease is variable depending on the underlying health of the individual - the young and old tend to be more severely affected. Infection usually occurs through the fecal-oral route. Infection can be transmitted between people unless appropriate hygiene measures are undertaken. Some infected patients are asymptomatic and are those more likely to transmit infection to other people.
  • Shigella sonnei: A form of bacterium
  • Shigella sonnei infection: Shigella sonnei is a species of bacteria from the Shigella genus. Sonnei is the most common cause of Shigellosis in the developed world. Infection with this bacteria causes diarrhea. The severity of the disease is variable depending on the underlying health of the individual - the young and old tend to be more severely affected. Infection usually occurs through the fecal-oral route. Infection can be transmitted between people unless appropriate hygiene measures are undertaken. Some infected patients are asymptomatic and are those more likely to transmit infection to other people.
  • Shigellosis: An infectious disease which affects the intestinal tract and is caused by the Shigella bacteria. The condition may be severe, especially in children, but may be asymptomatic in some cases. The disease can be transmitted through fecal-oral contact.
  • Short Bowel Syndrome: Disorder of shortened bowel usually from bowel surgery.
  • Shprintzen syndorme: An inherited syndrome of cardiac defects and craniofacial anomalies and various other abnormalities.
  • Small Intestine Cancer: Cancer of the small intestine.
  • Small intestine cancer, adult: Cancer (malignant) that develops in the small intestine of adults.
  • Sporadic colorectal cancer: Sporadic colon cancer occurs in people who have no (or very little) family history of the disease. Although colon cancer sometimes has a familial or hereditary component, it usually doesn't.The majority of colon cancer, about 75%, is sporadic.
  • Stevens Johnson syndrome: A rare but serious condition involving inflammation and blistering of the skin and mucous membranes. It is believed to be an allergic reaction that can occur in response to some drugs or infectious diseases.
  • Stomach Conditions: Any condition that affects a persons stomach
  • Stomach bleeding: A condition which is characterized by bleeding from the stomach
  • Stomach cancer: Stomach or gastric cancer can develop in any part of the stomach and may spread throughout the stomach and to other organs
  • Stomach cancer, familial: Cancer of the stomach that tends to run in families.
  • Stool symptoms: Changes to stool such as diarrhea
  • Sucrase-Isomaltase Deficiency: A condition which is characterized by a deficiency of sucrase-isomaltase deficiency
  • Sucrase-isomaltase malabsorption, congenital: A rare disorder where a congenital deficiency of an enzyme (sucrase-isomaltase) prevents the absorption of sucrose and isomaltose consumed in the diet.
  • Sucrase-isomaltose malabsorption, congenital: A rare disorder where a congenital deficiency of an enzyme (sucrase-isomaltase) prevents the absorption of sucrose and isomaltose consumed in the diet.
  • Sudden onset of anal itching: Sudden onset of anal itching refers to the rapid development of an itching sensation in the anus.
  • Sudden onset of anal rash: Sudden onset of anal rash refers to a rapid development of an eruption or skin reaction in and around the anus.
  • Sump Syndrome: A complication that can sometimes occur after an operation done to treat recurring stone disease. The surgery involves forming a connection between the common bile duct and the intestines. Sometimes a pit-like (sump) portion develops along the bile duct and this allows debris such as food to build up in a pit-like (sump) portion of the bile duct. The buildup of debris can lead to infection.
  • Susceptibility to Celiac Disease 1: Susceptibility to celiac disease 1 is a term allocated to a genetic defect on a particular chromosome (chromosome 6p21.3) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. 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.
  • Susceptibility to Celiac Disease 10: Susceptibility to celiac disease 10 is a term allocated to a genetic defect on a particular chromosome (chromosome 3q25-q26) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. 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.
  • Susceptibility to Celiac Disease 11: Susceptibility to celiac disease 11 is a term allocated to a genetic defect on a particular chromosome (chromosome 3q28) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. 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.
  • Susceptibility to Celiac Disease 12: Susceptibility to celiac disease 12 is a term allocated to a genetic defect on a particular chromosome (chromosome 6q25) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. 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.
  • Susceptibility to Celiac Disease 13: Susceptibility to celiac disease 13 is a term allocated to a genetic defect on a particular chromosome (chromosome 12q24) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. 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.
  • Susceptibility to Celiac Disease 2: Susceptibility to celiac disease 2 is a term allocated to a genetic defect on a particular chromosome (chromosome 5q31-q33) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. 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.
  • Susceptibility to Celiac Disease 3: Susceptibility to celiac disease 3 is a term allocated to a genetic defect on a particular chromosome (chromosome 2q33) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. 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.
  • Susceptibility to Celiac Disease 4: Susceptibility to celiac disease 4 is a term allocated to a genetic defect on a particular chromosome (chromosome 19p13.1) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. 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.
  • Susceptibility to Celiac Disease 5: Susceptibility to celiac disease 5 is a term allocated to a genetic defect on a particular chromosome (chromosome 15q11-q13) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. 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.
  • Susceptibility to Celiac Disease 6: Susceptibility to celiac disease 6 is a term allocated to a genetic defect on a particular chromosome (chromosome 4q27) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. 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.
  • Susceptibility to Celiac Disease 7: Susceptibility to celiac disease 7 is a term allocated to a genetic defect on a particular chromosome (chromosome 1q133) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. 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.
  • Susceptibility to Celiac Disease 8: Susceptibility to celiac disease 8 is a term allocated to a genetic defect on a particular chromosome (chromosome 2q11-q12) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. 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.
  • Susceptibility to Celiac Disease 9: Susceptibility to celiac disease 9 is a term allocated to a genetic defect on a particular chromosome (chromosome 3p21) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. 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.

Conditions listing medical symptoms: Anal symptoms:

The following list of conditions have 'Anal 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.

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

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

Conditions listing medical complications: Anal symptoms:

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

 

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

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