| 영문 | carbohydrate | 한글 | 탄수화물 |
|---|---|---|---|
| 설명 | 탄소와 물분자로 이루어진 유기화합물. 삼대영양소 가운데 하나로, 녹색식물의 광합성으로 생긴다. 포도당, 과당, 녹말 따위가 있다. 일반적으로 탄소-수소-산소의 세 원소로 이루어지는 화합물로, 넓은 뜻으로는 당류-당질과 같은 뜻으로 쓰인다. 일반식(Cn(H2O)n이 마치 탄소와 물분자(H2O)로 이루어져 있는 것처럼 보이기 때문에 이런 이름이 붙었다. 그리고 산소 원자수가 일반식보다 하나 적은 것, 질소원자를 함유하는 것, 황화합물을 함유하는 것도 탄수화물에 포함시킨다. 화학적으로는 다가 알코올의 알데히드 또는 케톤 및 그 유도체의 총칭이다. |
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| IEM | immuno-electron microscopy; inborn error of metabolism |
|---|---|
| CMI | carbohydrate metabolism index; care management integration; case mix index; cell-mediated immunity; ... |
| ADME | [drug] absorption, distribution, metabolism, and excretion |
| BM | Bachelor of Medicine; barium meal; basal medium; basal metabolism; basement membrane; basilar membra... |
| 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) |
| carbohydrate metabolism | <biochemistry> The breakdown of starches and sugars into smaller units that can be used by the body for energy. (27 Sep 1997) |
| 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) |
| antigens, tumour-associated, carbohydrate | Carbohydrate antigens expressed by malignant tissue. They are useful as tumour markers and are measured in the serum by means of a radioimmunoassay employing monoclonal antibodies. (12 Dec 1998) |
| carbohydrate | <biochemistry> Very abundant compounds, usually an aldehyde or ketone derivative of a polyhydric alcohol, particularly of the pentahydric and hexahydric alcohols. They are so named because the hydrogen and oxygen are usually in the proportion to form water with the general formula Cn(H2O)n. The most important carbohydrates are the starches, sugars, celluloses and gums. They are classified into mono, di, tri, poly and heterosaccharides. The smallest are monosaccharides like glucose whereas polysaccharides such as starch, cellulose or glycogen can be large and indeterminate in length. (08 Oct 1997) |
Synonyms : Carbohydrate Metabolism, Inborn Error
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|