293,031 терминов и синонимов из MeSH и LOINC
Lang Dictionary CODE | LUI | preferred no |
SUI | preference Yes / No |
Terms, descriptions |
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CUI C0007570 | |||||||
Russian | Medical Subject Headings Russian | D002446 | L3375969 | preferred | S3903461 | Y | ЦЕЛИАКИЯ |
Russian | Medical Subject Headings Russian | D002446 | L0906407 | no | S1110224 | Y | TSELIAKIIA |
Russian | Medical Subject Headings Russian | D002446 | L1511861 | no | S1807770 | Y | BOLEZN' GLIUTENOVAIA |
Russian | Medical Subject Headings Russian | D002446 | L1521997 | no | S1817906 | Y | GLIUTENOVAIA ENTEROPATIIA |
Russian | Medical Subject Headings Russian | D002446 | L1543111 | no | S1839020 | Y | SPRU |
Russian | MDRRUS | 10018461 | L15712403 | no | S19029157 | Y | Глютензависимая энтеропатия |
Russian | MDRRUS | 10029525 | L15715230 | no | S19051541 | Y | Нетропическая спру |
Russian | MDRRUS | 10007864 | L15723384 | no | S19029159 | Y | Глютенчувствительная целиакия |
Russian | MDRRUS | 10009839 | L15731432 | no | S19092780 | N | Целиакия |
Russian | MDRRUS | 10009839 | L15731432 | no | S19092780 | Y | Целиакия |
Russian | MDRRUS | 10058248 | L15764662 | no | S19092778 | Y | Целиакия спру |
Russian | MDRRUS | 10018458 | L15778706 | no | S19029158 | Y | Глютеновая энтеропатия |
Russian | MDRRUS | 10007865 | L15786580 | no | S19092779 | Y | Целиакия-спру |
Russian | Medical Subject Headings Russian | D002446 | L3341510 | no | S3868992 | Y | БОЛЕЗНЬ ГЛЮТЕНОВАЯ |
Russian | Medical Subject Headings Russian | D002446 | L3346045 | no | S3873528 | Y | ГЛЮТЕНОВАЯ ЭНТЕРОПАТИЯ |
Russian | Medical Subject Headings Russian | D002446 | L3370345 | no | 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. |