| GDH | glucose dehydrogenase; glutamate dehydrogenase; glycerophosphate dehydrogenase; glycol dehydrogenase... |
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| GPD | glucose-6-phosphate dehydrogenase; glycerol-phosphate dehydrogenase |
| LAD | lactic acid dehydrogenase; left anterior descending [artery]; left axis deviation; leukocyte adhesio... |
| LADH | lactic acid dehydrogenase; liver alcohol dehydrogenase |
| PDH | past dental history; phosphate dehydrogenase; position-of-the-dynamometer-handle [test]; progressive... |
| 11 beta-HSD | 11 Beta-hydroxysteroid dehydrogenase |
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| 11 beta-OHSD | 11 beta-Hydroxysteroid dehydrogenase |
| 11 beta-HSD-1 | 11 beta-Hydroxysteroid dehydrogenase type 1 |
| 11 beta-HSD2 | 11 beta-Hydroxysteroid dehydrogenase type 2 |
| 15-PGDH | 15-Hydroxy-prostaglandin dehydrogenase |
| glucose-6-phosphate dehydrogenase | <enzyme> An NADP+ enzyme that catalyses the dehydrogenation (oxidation) of d-glucose-6-phosphate to 6-phospho-d-glucono-d-lactone, this reaction initiating the Dickens shunt. Deficiency of this enzyme is the commonest disease-causing enzyme defect in humans affecting an estimated 400 million people. The gene for this enzyme is on the X chromosome. Males with the enzyme deficiency develop haemolytic anaemia when red blood cells are exposed to oxidant drugs such as the antimalarial primaquine, the sulfonamide antibiotics or sulfones, naphthalene moth balls, or fava beans. Synonym: Robison ester dehydrogenase, Zwischenferment. Acronym: G6PD (12 Sep 2002) |
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| glucose-6-phosphate dehydrogenase deficiency | A deficiency of glucose-6-phosphate dehydrogenase, an enzyme important for maintaining cellular concentrations of reduced nucleotides. Deficiency of this enzyme is the commonest disease-causing enzyme defect in humans affecting an estimated 400 million people. The gene for this enzyme is on the X chromosome and there are various polymorphic forms. Males with the enzyme deficiency develop haemolytic anaemia when red blood cells are exposed to oxidant drugs such as the antimalarial primaquine, the sulfonamide antibiotics or sulfones, naphthalene moth balls, or fava beans. It can also cause anaemia of the newborn, and chronic nonspherocytic haemolytic anaemia. Inheritance: X-linked. (12 Sep 2002) |
| acetaldehyde dehydrogenase | <enzyme> Works with both nad and nadp Registry number: EC 1.2.1.5 Synonym: aldehyde dehydrogenase (NADP+), naho gene product (26 Jun 1999) |
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| acetoin dehydrogenase | <enzyme> An enzyme that catalyses the conversion of acetoin to diacetyl in the presence of NAD. Chemical name: Acetoin:NAD+ oxidoreductase Registry number: EC 1.1.1.5 (12 Dec 1998) |
| acetol dehydrogenase | <enzyme> Forms methylglyoxal; uses nad+ Registry number: EC 1.1.1.- Synonym: 1-hydroxyacetone dehydrogenase (26 Jun 1999) |
| acyl-ACP dehydrogenase | enoyl-ACP reductase (NADPH) |
| acyl-CoA dehydrogenase | <enzyme> See also records for specific fatty acyl groups which have full EC nomenclature number; electron-transferring flavoprotein system reducing ubiquinone and other acceptors; formerly EC 1.3.2.2 Registry number: EC 1.3.99.3 Synonym: fatty-acyl CoA dehydrogenase, palmitoyl-CoA dehydrogenase, short-chain acyl-CoA dehydrogenase, acyl-coenzyme a dehydrogenase, lauroyl-CoA oxidase (26 Jun 1999) |
| acyl-CoA dehydrogenase (NADPH+) | Enzyme catalyzing the reversible reduction of enoyl-CoA derivatives of chain length 4 to 16, with NADPH as the hydrogen donor, forming acyl-CoA and NADP+. Synonym: enoyl-CoA reductase. (05 Mar 2000) |
| alanopine dehydrogenase | <enzyme> Catalyses reductive elimination between pyruvate and alanine, or glycine, utilizing NADH as coenzyme, producing 2,2'-iminodipropionic acid (alanopine) Registry number: EC 1.5.1.- (26 Jun 1999) |
| alcohol dehydrogenase | <enzyme> An enzyme that catalyses reversibly the final step of alcoholic fermentation by reducing an aldehyde to an alcohol. In the case of ethanol, acetaldehyde is reduced to ethanol in the presence of NADH and hydrogen. The enzyme is a zinc protein which acts on primary and secondary alcohols or hemiacetals. Chemical name: Alcohol:NAD+ oxidoreductase Registry number: EC 1.1.1.1 (12 Dec 1998) |
| alcohol dehydrogenase (acceptor) | An oxidoreductase that reversibly converts primary alcohols to aldehydes with an H acceptor other than NADP+. (05 Mar 2000) |
| alcohol dehydrogenase (NADP+) | An oxidoreductase reversibly converting alcohols to aldehydes (or ketones) with NAD(P)+ as H acceptor. Synonym: aldehyde reductase, DPNH aldehyde transhydrogenase. (05 Mar 2000) |
| aldehyde dehydrogenase | <enzyme> An enzyme that oxidises an aldehyde in the presence of NAD+ and water to an acid and NADH. Before 1978, it was classified as EC 1.1.1.70. Chemical name: Aldehyde:NAD+ oxidoreductase Registry number: EC 1.2.1.3 (12 Dec 1998) |
| aldehyde dehydrogenase (acylating) | An oxidoreductase converting an aldehyde and CoA to acyl-CoA with NAD+ as H acceptor. (05 Mar 2000) |
| aldehyde dehydrogenase (NAD+) | An oxidoreductase reversibly converting aldehydes to acids with NADP+ as H acceptor. (05 Mar 2000) |
| aldehyde dehydrogenase (NAD(P)+) | An oxidoreductase reversibly converting aldehydes to acids with NAD+ or NADP+ as H acceptor. (05 Mar 2000) |
| alloisocitrate dehydrogenase | <enzyme> Nad+ dependent Registry number: EC 1.1.1.- (26 Jun 1999) |
| glucose-6-phosphate dehydrogenase |
an enzyme involved in maintaining the membrane integrity of red blood cells. Deficiency of this enzyme is a sex-linked genetic condition which occurs with highest frequencies in people of African, Middle Eastern and Southeast Asian origin; it affects 12% of the US African-American male population. Some drugs and infections can cause red blood cells to burst, resulting in severe anemia and other complications among persons deficient in this enzyme.
출처: www.cdc.gov/ncidod/dvrd/rmsf/Glossary.htm
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| glucose-6-phosphate dehydrogenase deficiency |
a deficiency of an enzyme - G6PD - in red blood cells, causing hemolytic anemia.
출처: www.uchospitals.edu/online-library/content=P00090
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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