| AAMD | American Association on Mental Deficiency; 미국 정신 박약 협회 |
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| AAMD-ABS | American Association on Mental Deficiency-Adaptive Behavior Scale; 미국 정신 박약 협회 적응 행동 척도... |
| AIDS | Acquired Immuno(Immune)-Deficiency Syndrome; 후천성 면역 결핍 증후군 |
| IDA | 1) Imino-Diacetic Acid 2) Iron Deficiency Anemia &nb... |
| IGHD | Idiopathic Growth Hormone Deficiency |
| D-erythro-dihydroneopterin triphosphate epimerase | <enzyme> Forms l-threo-dihydroneopterin triphosphate Registry number: EC 5.1.99.- Synonym: 2-amino-4-hydroxy-6-(d-erythro-1',2',3'-trihydroxy- propyl)-7,8-dihydropteridine triphosphate epimerase, dihydroneopterin triphosphate epimerase, folx gene product (26 Jun 1999) |
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| dTDP-4-ketorhamnose 3,5-epimerase | <enzyme> Thymidine diphosphate sugars (75-82) is not an active mh Registry number: EC 5.1.3.13 Synonym: dtdp-4-dehydrorhamnose 3,5-epimerase (26 Jun 1999) |
| inositol NAD epimerase | <enzyme> Converts myo-inositol to scyllo-inositol and neoinositol; inosose also formed and reverse reaction Registry number: EC 1.1.1.- (26 Jun 1999) |
| isopenicillin N epimerase | <enzyme> From streptomyces clavuligerus; converts isopenicillin n to penicillin n Registry number: EC 5.1.1.- Synonym: cefd protein (26 Jun 1999) |
| thymidine-diphospho-4-keto-6-deoxyglucose epimerase | <enzyme> Isolated from saccharopolyspora erythraea; catalyses the formation of tdp-4-keto-l-rhamnose from thymidine-diphospho-4-keto-6-deoxy-d-glucose Registry number: EC 5.1.3.- Synonym: tdkd-glucose epimerase, tdp-4-keto-6-deoxyglucose 3,5-epimerase, kde gene product (26 Jun 1999) |
| epimerase | <enzyme> An enzyme that catalyses the reversible conversion of an epimer into its counterpart form. (09 Oct 1997) |
| UDP acetylglucosamine-2-epimerase | <enzyme> Catalyses the formation of n-acetylmannosamine and udp from udp n-acetylglucosamine; minor descriptor (75-82); online and index medicus search carbohydrate isomerases (75-82); minor descriptor (75-82); file maintained to carbohydrate isomerases Registry number: EC 5.1.3.14 Synonym: udp acetylglucosamine 2 epimerase, udp n-acetyl-d-glucosamine 2-epimerase (26 Jun 1999) |
| UDPgalactose 4-epimerase | <enzyme> A necessary enzyme in the metabolism of galactose. It reversibly catalyses the conversion of udpglucose to udpgalactose. NAD+ is an essential component for enzymatic activity. Chemical name: UDPglucose 4-epimerase Registry number: EC 5.1.3.2 (12 Dec 1998) |
| udpglucose 4-epimerase | <enzyme> A necessary enzyme in the metabolism of galactose. It reversibly catalyses the conversion of udpglucose to udpgalactose. NAD+ is an essential component for enzymatic activity. Chemical name: UDPglucose 4-epimerase Registry number: EC 5.1.3.2 (12 Dec 1998) |
| UDPglucuronate 4-epimerase | <enzyme> Uridine diphosphate glucuronic aid (77-82) is not an active mh Chemical name: udpgalacturonate 4-epimerase Registry number: EC 5.1.3.6 (26 Jun 1999) |
| uridine diphosphoglucose 4-epimerase | <enzyme> A necessary enzyme in the metabolism of galactose. It reversibly catalyses the conversion of udpglucose to udpgalactose. NAD+ is an essential component for enzymatic activity. Chemical name: UDPglucose 4-epimerase Registry number: EC 5.1.3.2 (12 Dec 1998) |
| 2-arylpropionyl-CoA epimerase | <enzyme> From rat liver cytosol and mitochondria; catalyses a rapid interconversion between the r- and s-epimers of 2-arylpropionic acids which upon the action of a thioesterase on the r-isomer yields the free acid Registry number: EC 5.1.99.- (26 Jun 1999) |
| L-ribulosephosphate 4-epimerase | <enzyme> Consider also EC 5.1.3.1,ribulosephosphate 3-epimerase Registry number: EC 5.1.3.4 Synonym: l-ribulose 5-phosphate 4-epimerase, rpe1 gene product (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) |