| 영문 | standard error | 한글 | 표준오차 |
|---|---|---|---|
| 설명 | 통계용어로 표본 평균치 분포의 표준편차를 나타내는 것이다. 표본 평균치가 모집단의 평균치 주위에 산재하는 것은 표본 크기와 모집단의 표준편차(σ)에 의해 지배된다. 표준오차(SD)는 이론적으로 σ/√N으로 나타낸다. |
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| IEM | immuno-electron microscopy; inborn error of metabolism |
|---|---|
| FPE | fatal pulmonary embolism; field placement error; final prediction error |
| SE | saline enema; sanitary engineering; side effect; smoke exposure; solid extract; sphenoethmoidal; spi... |
| SEM | sample evaluation method; scanning electron microscopy; secondary enrichment medium; standard error ... |
| ALE | active life expectancy; allowable limits of error; amputated lower extremity |
| IEM | Inborn Errors of Metabolism |
|---|---|
| SEM | 1-standard error of measurement |
| CE | Constant error |
| ERN | Error-related negativity |
| MSE | Mean Square Error |
standard error
| inborn error of metabolism | A genetic biochemical disorder of a specific enzyme that forms a metabolic block, e.g., phenylketonuria. (05 Mar 2000) |
|---|---|
| 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) |
| 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) |
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| 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 | 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) |
| 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) |
| alpha error | The statistical error (said to be of the first kind or type I) made in testing an hypothesis when it is concluded that a result is positive when it really is not. Alpha error is often referred to as a false positive. (12 Dec 1998) |
| beta error | The statistical error (said to be of the second kind or type II) made in testing when it is concluded that something is negative when it really is positive. Beta error is often referred to as a false negative. (12 Dec 1998) |
| residual error | The estimated discrepancy between the actual measured datum and the value for that value computed after a model has been fitted to the set of the data by an estimator. (05 Mar 2000) |
| standard error of difference | A statistical index of the probability that a difference between two sample means is greater than zero. (05 Mar 2000) |
| standard error of the mean | A statistical index of the probability that a given sample mean is representative of the mean of the population from which the sample was drawn. (05 Mar 2000) |
| interobserver error | The differences in interpretation by two or more individuals making observations of the same phenomenon. (05 Mar 2000) |
| intraobserver error | The differences in interpretation by an individual making observations of the same phenomenon at different times. (05 Mar 2000) |
| technical error | That component of experimental error that is due to the conduct of the experiment and in principle estimated by replicate determinations on aliquots from the same specimen. (05 Mar 2000) |
| trial and error | The apparently random, haphazard, hit-or-miss exploratory activity which often precedes the acquisition of new information or adjustments; it may be overt, as in a rat running in a maze, or covert (vicarious), as when one thinks of various ways of coping with a situation. (05 Mar 2000) |
| inborn error of metabolism |
any of a number of diseases in which an inherited defect (usually a missing or inadequate enzyme) results in an abnormality of metabolism
출처: wordnet.princeton.edu/perl/webwn
|
|---|---|
| inborn error of metabolism |
Inborn errors of metabolism comprise a large class of genetic diseases involving disorders of metabolism. The majority are due to defects of single genes that code for enzymes that facilitate conversion of various substances (substrates) into others (products). In most of the disorders, problems arise due to accumulation of substances which are toxic or interfere with normal function, or to the effects of reduced ability to synthesize essential compounds. ...
출처: en.wikipedia.org/wiki/Inborn_error_of_metabolism
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| inborn error of metabolism |
a disorder caused by an inherited defect in an enzyme pathway which affects the body's metabolism.
출처: www.uchicagokidshospital.org/online-library/conten...
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| inborn error of m. |
see under error.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| inborn error | any of a number of diseases in which an inherited defect (usually a missing or inadequate enzyme) results in an abnormality of metabolism |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|