| CLF | cardiolipin fluorescent [antibody]; ceroid lipofuscinosis; cholesterol-lecithin flocculation |
|---|---|
| CNL | cardiolipin natural lecithin; chronic neutrophilic leukemia |
| CSL | cardiolipin synthetic lecithin; corticosteroid liposome |
| DPL | diagnostic peritoneal lavage; dipalmitoyl lecithin; distopulpolingual |
| LCATA | lecithin cholesterol acetyltransferase alpha |
| sterol o-acyltransferase | <enzyme> An enzyme that catalyses the formation of cholesterol esters by the direct transfer of the fatty acid group from a fatty acyl CoA derivative. This enzyme has been found in the adrenal gland, gonads, liver, intestinal mucosa, and aorta of many mammalian species. Chemical name: Acyl-CoA:cholesterol O-acyltransferase Registry number: EC 2.3.1.26 (12 Dec 1998) |
|---|---|
| N-hydroxy-2-acetylaminofluorene N-O-acyltransferase | <enzyme> From rat liver; forms non-mutagenic n-o-acetyl-2-acetylaminofluorene Registry number: EC 2.3.1.- Synonym: n-oh-aaf n-o-acyltransferase, haf-acyltransferase (26 Jun 1999) |
| delta5-3beta-hydroxysteroid acyltransferase | <enzyme> Forms esters of palmitate, oleate, linoleate, stearate and myristate with pregnenolone or dehydroepiandrosterone; from rat brain microsomes Registry number: EC 2.3.1.- Synonym: pregnenolone o-acyltransferase, dehydroepiandrosterone o-acyltransferase (26 Jun 1999) |
| dihydrolipoamide acyltransferase | <enzyme> Component of branched-chain 2-oxo acid dehydrogenase multienzyme complex; mutation in this (e2) catalytic subunit identifies type II maple syrup urine disease Registry number: EC 2.3.1.- Synonym: dihydrolipoyl transacylase, branched chain acyltransferase, e2 transacylase (26 Jun 1999) |
| ergosterol acyltransferase | <enzyme> From saccharomyces cerevisiae; catalyses the esterification of ergosterol Registry number: EC 2.3.1.- Synonym: acyl CoA-ergosterol acyltransferase, acyl coenzyme a-ergosterol acyltransferase (26 Jun 1999) |
| ethanol acyltransferase | <enzyme> Forms ethyl palmitate; responsible in part for the synthesis of fattyl acid ethyl esters; uses ethanol and fatty acyl-CoA as substrates Registry number: EC 2.3.1.- Synonym: acyl coenzyme a-ethanol acyltransferase, acyl CoA-ethanol acyltransferase (26 Jun 1999) |
| 1-acylglycerophosphocholine o-acyltransferase | <enzyme> An enzyme localised predominantly within the plasma membrane of lymphocytes. It catalyses the transfer of long-chain fatty acids, preferentially unsaturated fatty acids, to lysophosphatides with the formation of 1,2-diacylglycero-3-phosphocholine and CoA. Chemical name: Acyl-CoA:1-acyl-sn-glycero-3-phosphocholine O-acyltransferase Registry number: EC 2.3.1.23 (12 Dec 1998) |
| 1-acyl-glycerophosphoethanolamine acyltransferase | <enzyme> Guinea pig heart microsome enzyme; not the same as EC 2.3.1.25 (plasmalogen synthase) Registry number: EC 2.3.1.- Synonym: acyl-CoA-1-acylglycerophosphoethanolamine 2-acyltransferase, 1-agpe acyltransferase, acyl-coenzyme a-1-acylglycerophosphoethanolamine 2-acyltransferase (26 Jun 1999) |
| long-chain-alcohol O-fatty-acyltransferase | <enzyme> Catalyses the final step in biosynthesizing storage liquid waxes from long chain fatty acyl CoA and fatty alcohols; forming predominantly c42 wax esters Registry number: EC 2.3.1.75 Synonym: acyl-coenzyme a-alcohol transacylase, aca transacylase, acyl-CoA-alcohol transacylase, wax-ester synthase (26 Jun 1999) |
| lysomonogalactosyldiacylglycerol acyltransferase | <enzyme> Transfers acyl group from acyl-acyl-carrier protein to an endogenous lysomonogalactosyldiacylglycerol to form monogalactosyldiacylglycerol Registry number: EC 2.3.1.- Synonym: acp-lysomgdg acyltransferase, monogalactosyldiacylglycerol synthase, mgdg synthase (26 Jun 1999) |
| lysophosphatidic acid acyltransferase | 1-acylglycerol-3-phosphate acyltransferase. (05 Mar 2000) |
| 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) |