| TCP | T-complex protein; therapeutic continuous penicillin; total circulating protein; transcutaneous pace... |
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| AAMD | American Association on Mental Deficiency; ¹Ì±¹ Á¤½Å ¹Ú¾à Çùȸ |
| AAMD-ABS | American Association on Mental Deficiency-Adaptive Behavior Scale; ¹Ì±¹ Á¤½Å ¹Ú¾à Çùȸ ÀûÀÀ Çൿ ôµµ... |
| AIDS | Acquired Immuno(Immune)-Deficiency Syndrome; ÈÄõ¼º ¸é¿ª °áÇÌ ÁõÈıº |
| IDA | 1) Imino-Diacetic Acid 2) Iron Deficiency Anemia &nb... |
| 2-hydroxychromene-2-carboxylate isomerase | <enzyme> Catalyses the conversion of 2-hydroxychromene-2-carboxylate to cis-o-hydroxybenzylidenepyruvate--a step in the bacterial degradation of naphthalene to salicylate Registry number: EC 5.3.99.- Synonym: o-hydroxychromene-2-carboxylate isomerase, hcca isomerase (26 Jun 1999) |
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| 2-hydroxyhepta-2,4-diene-1,7-dioate isomerase | <enzyme> Exists as a bifunctional enzyme with 5-oxopent-3-ene-1,2,5-tricarboxylate decarboxylase (EC 4.1.1.68) in the homoprotocatechuate degradative pathway of E coli. Registry number: EC 5.3.3.- Synonym: hhdd isomerase (26 Jun 1999) |
| 3 beta-hydroxysteroid oxidoreductase-delta(5) 3-ketosteroid isomerase | <chemical> System found in breast cancers; consists of EC 1.1.1.145 (progesterone reductase) and EC 5.3.3.1 (steroid delta-isomerase)) Synonym: 3 ohsteroid dehydrogenase-isomerase, delta 5-3 beta hydroxysteroid dehydrogenase-isomerase, 3 beta-hydroxysteroid dehydrogenase-isomerase, 3 beta-hydroxysteroid dehydrogenase-delta(5)-delta(4)-isomerase, 3 beta-hydroxysteroid dehydrogenase-5--4-ene-isomerase, 3-beta-hydroxysteroid dehydrogenase-delta(5-4)-isomerase, 3 beta hydroxysteroid dehydrogenase-delta5-delta4-isomerasease, 3 beta-ol dehydrogenase-delta(4)-delta(5) isomerase, 3 beta-hydroxy-5-ene steroid dehydrogenase-delta 5-delta 4 isomerase (26 Jun 1999) |
| 3-methylitaconate delta-isomerase | <enzyme> Catalyses reversibly the isomerization of methylitaconate to dimethylmaleate Registry number: EC 5.3.3.6 Synonym: 3-midiase (26 Jun 1999) |
| 4-carboxymethyl-methylbut-2-ene-1,4-olide isomerase | <enzyme> From alcaligenes eutrophus; catalyses the formation of 3-methyl-2-ene-lactone from 4-methyl-2-ene-lactone Registry number: EC 5.4.99.- Synonym: 4-methyl-2-enelactone isomerase (26 Jun 1999) |
| 4-deoxy-L-threo-5-hexosulose-uronate ketol-isomerase | <enzyme> Converts 5-keto-4-deoxyuronate to 2,5-diketo-3-deoxygluconate Registry number: EC 5.3.1.17 Synonym: 5-keto-4-deoxyuronate isomerase (26 Jun 1999) |
| 4-methylmuconolactone methyl-isomerase | <enzyme> From nocardioform actinomycetes; forms 3-methylmuconolactone Registry number: EC 5.3.3.- Synonym: 4-methyl-2-enelactone methylisomerase, mmlm-isomerase (26 Jun 1999) |
| 5-carboxymethyl-2-hydroxymuconate delta-isomerase | <enzyme> Catalyses the isomerization of 5-carboxymethyl-2-hydroxymuconate to yield 5-carboxymethyl-2-oxo-hex-3-ene-1,6-dioate Registry number: EC 5.3.3.10 Synonym: 5-cmhm isomerase, 5-carboxymethyl-2-hydroxymuconate isomerase (26 Jun 1999) |
| leukotriene B4 6-isomerase | <enzyme> From rat kidney homogenates Registry number: EC 5.2.- (26 Jun 1999) |
| L-rhamnose isomerase | <enzyme> Specified by structural gene rhaa from E coli; catalyses the conversion of l-rhamnose to l-rhamnulose Registry number: EC 5.3.1.14 Synonym: l-rhamnose ketol-isomerase (26 Jun 1999) |
| lycopene cyclase-isomerase | <enzyme> Found in bacteria chloroplasts; both isomerization and cyclization takes place; NADPH is essential cofactor; may be route to formation of alpha and beta carotene; has been sequenced; genbank d83513 Registry number: EC 5.5.- Synonym: crty protein, lycopene cyclase, crtl gene product, lycopene beta-cyclase (26 Jun 1999) |
| abdominal muscle deficiency syndrome | <syndrome> Congenital absence (partial or complete) of abdominal muscles, in which the outline of the intestines is visible through the protruding abdominal wall; in males, genitourinary anomalies (urinary tract dilation and cryptorchidism) are also found; genetics unclear. (05 Mar 2000) |
| adult lactase deficiency | Onset of lactase deficiency, with resulting milk intolerance and malabsorption, in adulthood. Inherited forms may not be manifested until adulthood; any process that damages the intestinal lining cells can cause lactase deficiency in adults. (05 Mar 2000) |
| alpha-1 antitrypsin deficiency | <chest medicine> Deficiency of the protease inhibitor alpha-1 antitrypsin, leads primarily to degradation of elastin of the alveolar walls, as well as other structural proteins of a variety of tissues. The lack of this protein leads to damage of various organs, but mainly to the lung and liver. symptoms may become apparent at a very early age or in adulthood, manifesting either as shortness of breath or liver related symptoms (jaundice, fatigue, fluid in the abdomen, mental changes, or gastrointestinal bleeding). There are several options for treatment of the lung disease, including replacement of the missing protein. Treatment of the liver disease is a well-timed liver transplant (12 Dec 1998) |
| alpha-1-proteinase deficiency | Absence of a serum proteinase inhibitor that may cause nodular non-suppurative panniculitis. (05 Mar 2000) |
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