| 영문 | variant | 한글 | 변형, 변이 |
|---|---|---|---|
| 설명 | 1.소속하는 부류와 다른 성질을 갖는 것의 총칭, 또는 일부 특별한 성질만 틀리는 것에 사용되는 단어. 2. 생물학상 동종의 생물에서 볼 수 있는 형질의 차이. |
||
| L-variant | a defective bacterial variant that can multiply on hypertonic medium |
|---|---|
| ECG | Electro-Cardio-Graphy(-Gram); 심전도 = EKG 1. Conducting System Structu... |
| GH-V | variant form of Growth Hormone |
| CBGv | corticosteroid-binding globulin variant |
| EEGV1 | electroencephalographic variant pattern 1 |
| V | A-variant |
|---|---|
| CD44v | CD44 variant |
| CD44v | CD44 variant isoform |
| CVA | Cough variant asthma |
| LBV | Lewy Body Variant |
| GM2 gangliosidosis | One of the hereditary metabolic disorders; several forms exist, including Tay-Sachs disease, Sandhoff's disease, AV variant and adult onset; characterised by accumulation of a specific metabolite, GM2 ganglioside due to deficiency of hexosaminidase A or B, or GM2 activator factor. (05 Mar 2000) |
|---|---|
| infantile GM2 gangliosidosis | <disease> A genetic disorder found in east European Jewish families which can result in early death bu affecting the brain and nerves by causing abnormal lipid metabolism. It is a lysosomal disease in which there is a deficiency of hexosaminidase A, an enzyme that degrades ganglioside GM2. Symptoms appear at age 3-6 months and include blindness, deafness, seizures, paralysis, dementia, decreased muscle tone and growth retardation. There is no known treatment and most children usually die between 2 and 5 years of age. Inheritance: autosomal recessive. (06 Oct 1997) |
| GM2-N-acetyl-beta-D-galactosaminidase | <enzyme> May be an aspect of hexosaminidase a Registry number: EC 3.2.1.- Synonym: gm2-ag-aminidase, ganglioside gm2 hydrolase (26 Jun 1999) |
| angina pectoris, variant | A clinical syndrome characterised by development of chest pain at rest with concomitant transient st segment elevation in the electrocardiogram, but exercise capacity is well preserved. (12 Dec 1998) |
| variant | Something which differs in form from another thing, though really the same; as, a variant from a type in natural history; a variant of a story or a word. Origin: Cf. F. Variante. Source: Websters Dictionary (01 Mar 1998) |
| variant angina | A sudden vasoconstriction of a coronary artery depriving the myocardium of blood flow and oxygen. This may clinically manifest as chest pain referred to as variant angina or Printzmetal's angina. May be precipitated by emotional stress, medications, street drugs (cocaine) or on exposure to cold. Treatment includes nitroglycerin or beta-blocker medications. (27 Sep 1997) |
| variant angina pectoris | A form of angina pectoris, characterised by pain that is not precipitated by cardiac work, is of longer duration, is usually more severe, and is associated with unusual electrocardiographic manifestations including elevated ST segments in leads that are ordinarily depressed in typical angina, and usually without reciprocal ST changes; occurring at night in bed. Synonym: angina inversa, variant angina pectoris. (05 Mar 2000) |
| variant haemoglobin | A harmless mutant form of Hb. (05 Mar 2000) |
| variant surface glycoproteins, trypanosoma | Glycoproteins attached to the surface coat of the trypanosome. Many of these glycoproteins show amino acid sequence diversity expressed as antigenic variations. This continuous development of antigenically distinct variants in the course of infection ensures that some trypanosomes always survive the development of immune response to propagate the infection. (12 Dec 1998) |
| gangliosidosis | Any disease characterised, in part, by the abnormal accumulation within the nervous system of specific gangliosides, e.g., GM2 gangliosidosis, Tay-Sachs disease, caused by hexosaminidase A enzyme deficiency with accumulation of GM2 ganglioside Synonym: gangliosialidosis, ganglioside lipidosis. (05 Mar 2000) |
| gangliosidosis g(m1) | Form of gangliosidosis characterised by accumulation of g(m1) ganglioside and oligosaccharides, and caused by an absence or severe deficiency of beta-galactosidase a. The three phenotypes of g(m1) gangliosidosis are called infantile (generalised), juvenile, and adult (types 1, 2, and 3 respectively), referring to the age at which clinical manifestations appear. (12 Dec 1998) |
| generalised gangliosidosis | Three forms exist: infantile, generalised; juvenile; and adult; gangliosidosis characterised by accumulation of a specific monosialoganglioside, GM1; due to deficiency of GM1-beta-galactosidase. Synonym: generalised gangliosidosis. (05 Mar 2000) |
| GM1 gangliosidosis | Three forms exist: infantile, generalised; juvenile; and adult; gangliosidosis characterised by accumulation of a specific monosialoganglioside, GM1; due to deficiency of GM1-beta-galactosidase. Synonym: generalised gangliosidosis. (05 Mar 2000) |
| infantile generalised GM1 gangliosidosis | One of the hereditary metabolic diseases of infancy; resembles Tay-Sachs disease, except other organ systems (bone, liver, kidney) are affected. Synonym: familial neuroviscerolipidosis, pseudo-Hurler disease, Type 1 GM1 gangliosidosis. (05 Mar 2000) |
| Type 1 GM1 gangliosidosis | One of the hereditary metabolic diseases of infancy; resembles Tay-Sachs disease, except other organ systems (bone, liver, kidney) are affected. Synonym: familial neuroviscerolipidosis, pseudo-Hurler disease, Type 1 GM1 gangliosidosis. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|