C0007570 - An autoimmune genetic disorder with an unknown pattern of inheritance that primarily affects the digestive tract. It is caused by intolerance to dietary gluten. Consumption of gluten protein triggers an immune response which damages small intestinal villi and prevents adequate absorption of nutrients. Clinical signs include abdominal cramping, diarrhea or constipation and weight loss. If untreated, the clinical course may progress to malnutrition, anemia, osteoporosis and an increased risk of intestinal malignancies. However, the prognosis is favorable with successful avoidance of gluten in the diet. 1/10
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CUI    C0007570
RussianMedical Subject Headings Russian D002446 L3375969preferred S3903461 Y ЦЕЛИАКИЯ
RussianMedical Subject Headings Russian D002446 L0906407no S1110224 Y TSELIAKIIA
RussianMedical Subject Headings Russian D002446 L1511861no S1807770 Y BOLEZN' GLIUTENOVAIA
RussianMedical Subject Headings Russian D002446 L1521997no S1817906 Y GLIUTENOVAIA ENTEROPATIIA
RussianMedical Subject Headings Russian D002446 L1543111no S1839020 Y SPRU
RussianMDRRUS 10018461 L15712403no S19029157 Y Глютензависимая энтеропатия
RussianMDRRUS 10029525 L15715230no S19051541 Y Нетропическая спру
RussianMDRRUS 10007864 L15723384no S19029159 Y Глютенчувствительная целиакия
RussianMDRRUS 10009839 L15731432no S19092780 N Целиакия
RussianMDRRUS 10009839 L15731432no S19092780 Y Целиакия
RussianMDRRUS 10058248 L15764662no S19092778 Y Целиакия спру
RussianMDRRUS 10018458 L15778706no S19029158 Y Глютеновая энтеропатия
RussianMDRRUS 10007865 L15786580no S19092779 Y Целиакия-спру
RussianMedical Subject Headings Russian D002446 L3341510no S3868992 Y БОЛЕЗНЬ ГЛЮТЕНОВАЯ
RussianMedical Subject Headings Russian D002446 L3346045no S3873528 Y ГЛЮТЕНОВАЯ ЭНТЕРОПАТИЯ
RussianMedical Subject Headings Russian D002446 L3370345no S3897835 Y СПРУ
Medical Subject Headings A0036279 AT127396928 A malabsorption syndrome that is precipitated by the ingestion of foods containing GLUTEN, such as wheat, rye, and barley. It is characterized by INFLAMMATION of the SMALL INTESTINE, loss of MICROVILLI structure, failed INTESTINAL ABSORPTION, and MALNUTRITION.
(CPTSP) CRISP Thesaurus A0475635 AT51223642 disease occurring in children and adults characterized by sensitivity to gluten, with chronic inflammation and atrophy of the mucosa of the upper small intestine; manifestations include diarrhea, malabsorption, steatorrhea, and nutritional and vitamin deficiencies.
Medical Subject Headings Czech A13061797 AT231378362 Onemocnění způsobující poruchu střevního vstřebávání (primární malabsorpční syndrom). Jeho podstatou je nesnášenlivost glutenu, resp. jeho složky gliadinu na imunologickém podkladě, vyvolávající zánětlivé postižení v oblasti tenkého střeva (zejm. jejuna). Histopatologicky je atrofie klků, lymfoplasmocytární infiltrace, poruchy enzymů. Onemocnění začíná častěji v dětství, ale výskyt v dospělosti není vůbec neobvyklý a uplatňují se u něj dědičné vlivy (některé HLA antigeny - zejm. HLA-DQ2). Příznaky malabsorpce (průjmy, nedostatek živin z porušeného vstřebávání, anemie, kostní změny, neuropatie, hubnutí aj.) se objevují po požití potravin obsahujících lepek a mizí po jeho vyloučení ze stravy. Časté a mnohdy převládající však jsou příznaky extraintestinální, zejm. kloubní, kožní (Duhringova herpetitformní dermatitida). V diagnóze je důležitá enterobiopsie (atrofie sliznice, zánětlivá infiltrace, enzymatické změny), vyšetření některých protilátek (proti gliadinu, endomyosinu, tkáňové transglutamináze) a vyšetření malabsorpce (např. xylosový test). Základem léčby je dieta s vyloučením lepku (tj. zákaz potravin z pšeničné a žitné mouky), jejíž dodržování výrazně zlepšuje prognózu. Je možné jej nahradit moukou kukuřičnou, sójou, rýží, bramborami. Karence se léčí substitucí, v těžších případech se podávají přechodně kortikoidy. Průběh choroby je kolísavý a různě těžký, obv. chronický s možnými relapsy i po expozici malému množství glutenu. Některé formy onemocnění mohou mít lehčí průběh a unikat diagnóze. U části pacientů se objevují i některé další poruchy imunitního systému (diabetes mellitus 1. typu, SLE, autoimunitní tyroiditida aj.); je častější výskyt malignit (lymfomy střeva i karcinomy) (cit. Velký lékařský slovník online, 2017 http://lekarske.slovniky.cz)
MEDLINEPLUS A21144506 AT230154344

Celiac disease is an immune disease in which people can't eat gluten because it will damage their small intestine. If you have celiac disease and eat foods with gluten, your immune system responds by damaging the small intestine. Gluten is a protein found in wheat, rye, and barley. It may also be in other products like vitamins and supplements, hair and skin products, toothpastes, and lip balm.

Celiac disease affects each person differently. Symptoms may occur in the digestive system, or in other parts of the body. One person might have diarrhea and abdominal pain, while another person may be irritable or depressed. Irritability is one of the most common symptoms in children. Some people have no symptoms.

Celiac disease is genetic. Blood tests can help your doctor diagnose the disease. Your doctor may also need to examine a small piece of tissue from your small intestine. Treatment is a diet free of gluten.

NIH: National Institute of Diabetes and Digestive and Kidney Diseases

HPO A24668654 AT206291272 Celiac disease (CD) is an autoimmune condition affecting the small intestine, triggered by the ingestion of gluten, the protein fraction of wheat, barley, and rye. Clinical manifestations of CD are highly variable and include both gastrointestinal and non-gastrointestinal features. The hallmark of CD is an immune-mediated enteropathy. This term is included because the occurence of CD is seen as a feature of a number of other diseases. [HPO:probinson, pmid:23681421]
NCI NCI Dictionary of Cancer Terms A7569404 AT198041568 A digestive disease that is caused by an immune response to a protein called gluten, which is found in wheat, rye, barley, and oats. Celiac disease damages the lining of the small intestine and interferes with the absorption of nutrients from food. A person with celiac disease may become malnourished no matter how much food is consumed.
NCI Thesaurus A7569404 AT198078276 An autoimmune genetic disorder with an unknown pattern of inheritance that primarily affects the digestive tract. It is caused by intolerance to dietary gluten. Consumption of gluten protein triggers an immune response which damages small intestinal villi and prevents adequate absorption of nutrients. Clinical signs include abdominal cramping, diarrhea or constipation and weight loss. If untreated, the clinical course may progress to malnutrition, anemia, osteoporosis and an increased risk of intestinal malignancies. However, the prognosis is favorable with successful avoidance of gluten in the diet.