| 영문 | lipid | 한글 | 지질 |
|---|---|---|---|
| 설명 | 생물체 안에 존재하며 물에 녹지 아니하고, 유기용매에 녹는 유기화합물을 통틀어 이르는 말. 좁은 의미로는 물에 녹지 않고 알코올, 콜로로포름이나 에테르, 벤젠 등의 비극성용매에 녹는 지방산의 에스테르로 생체에 이용되는 유기화합물이다. 단순지질, 복합지질(인지질, 당지질, 지단백) 및 유도지질(지질의 가수분해산물)로 분류된다. 특히 중성지방은 지방산과 글리세린과의 에스테르로 단백질과 당과 함께 생체의 주요성분 및 에너지원으로서 중요하다. 광의로는 스테로이드 등을 포함해서 호르몬, 비타민 류로서 작용하는 것 등으로 다양한 생리학적 기능을 담당하고 있다. |
||
| IEM | immuno-electron microscopy; inborn error of metabolism |
|---|---|
| ADME | [drug] absorption, distribution, metabolism, and excretion |
| BM | Bachelor of Medicine; barium meal; basal medium; basal metabolism; basement membrane; basilar membra... |
| CMI | carbohydrate metabolism index; care management integration; case mix index; cell-mediated immunity; ... |
| DIM | divalent ion metabolism; medium infective dose [Lat. dosis infectionis media] |
| IEM | Inborn Errors of Metabolism |
|---|---|
| PE | Prediction errors |
| RMSE | Root mean square errors |
| ADME | Absorption, distribution, metabolism, and excretion |
| CAM | Crassulacean Acid Metabolism |
| pyruvate metabolism, inborn errors | Hereditary disorders of pyruvate metabolism. They are difficult to diagnose and describe because pyruvate is a key intermediate in glycolysis, gluconeogenesis, and the tricarboxylic acid cycle. Some inherited metabolic disorders may alter pyruvate metabolism indirectly. Disorders in pyruvate metabolism appear to lead to deficiencies in neurotransmitter synthesis and, consequently, to nervous system disorders. (12 Dec 1998) |
|---|---|
| inborn errors of metabolism | Term coined by A. Garrod in 1908 applying to heritable disorders of biochemistry. Examples include albinism, cystinuria (a cause of kidney stones) and phenylketonuria (pku) are a few of the hundreds of inborn errors of metabolism. (12 Dec 1998) |
| fructose metabolism, inborn errors | Inherited abnormalities of fructose metabolism, which include three known autosomal recessive types: hepatic fructokinase deficiency (essential fructosuria), hereditary fructose intolerance, and hereditary fructose-1,6-diphosphatase deficiency. Essential fructosuria is a benign asymptomatic metabolic disorder caused by deficiency in fructokinase, leading to decreased conversion of fructose to fructose-1-phosphate and alimentary hyperfructosaemia, but with no clinical dysfunction; may produce a false-positive diabetes test. (12 Dec 1998) |
| renal tubular transport, inborn errors | Genetically determined disorders of the reabsorptive functions of the kidney with regard to specific nephron segments responsible for specific transport functions, classifiable by proximal nephron function, loop of henle function, and distal nephron function. The transport defects can be selective or nonselective. (12 Dec 1998) |
| inborn error of metabolism | A genetic biochemical disorder of a specific enzyme that forms a metabolic block, e.g., phenylketonuria. (05 Mar 2000) |
| refractive errors | Deviations from the average or standard indices of refraction of the eye through its dioptric or refractive apparatus. (12 Dec 1998) |
| medical errors | Errors or mistakes committed by health professionals which result in harm to the patient. They include errors in diagnosis (diagnostic errors), errors in the administration of drugs and other medications (medication errors), errors in the performance of surgical procedures, in the use of other types of therapy, in the use of equipment, and in the interpretation of laboratory findings. Medical errors are differentiated from malpractice in that the former are regarded as honest mistakes or accidents while the latter is the result of negligence, reprehensible ignorance, or criminal intent. (12 Dec 1998) |
| medication errors | Errors in prescribing, dispensing, or administering medication with the result that the patient fails to receive the correct drug or the proper dose of the drug in the treatment of his disease. (12 Dec 1998) |
| diagnostic errors | Incorrect diagnoses after clinical examination or technical diagnostic procedures. (12 Dec 1998) |
| inborn | Born in or with; implanted by nature; innate; as, inborn passions. Synonym: Innate, inherent, natural. (27 Oct 1998) |
| inborn lysosomal disease | Inherited disorder of one or more degradative enzymes normally located in lysosomes leading to accumulation (storage) of abnormal quantities of a substance, such as a glycosaminoglycan as in Hurler's syndrome or a lipopolysaccharide as in Gaucher's disease. (05 Mar 2000) |
| inborn reflex | A reflex such as breathing that is innate. (05 Mar 2000) |
| basal metabolism | <biochemistry, biology> Heat production, or its measurement, of an organism at the lowest level of cell chemistry in an inactive, awake, fasting state. It may be determined directly by means of a calorimeter or indirectly by calculating the heat production from an analysis of the end products of oxidation within the organism or from the amount of oxygen utilised. (27 Jun 1999) |
| calcium metabolism | A set of biochemical processes which act to keep the level of calcium in the blood at a constant level, with enough around to build bones and teeth. (09 Oct 1997) |
| calcium metabolism disorders | Disorders in the processing of calcium in the body: its absorption, transport, storage, and utilization. (12 Dec 1998) |
Synonyms : Lipid Metabolism, Inborn Error
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|