| 영문 | triglyceride | 한글 | 트리글리세리드 |
|---|---|---|---|
| 설명 | 글리세린과 3분자의 지방산이 에스테르화결합한 화합물. 탄수화물로부터 합성되는 중성지방. 동물의 지방조직에 저장하기 때문에, 효소에 의한 가수분해로 유리지방산을 혈액중에 방출한다. |
||
| 영문 | hepatic duct | 한글 | 간관 |
|---|---|---|---|
| 설명 | 간에서 생성된 담즙이 지나는 통로로 간에서 직접 담즙을 운반하는 관을 말한다. 간에서 만들어진 담즙은 간관, 쓸개주머니관를 거쳐서 쓸개에 보관되었다가 온쓸개관을 통해서 샘창자로 보내진다.  |
||
| 영문 | hepatic portal system | 한글 | 간문맥계 |
|---|---|---|---|
| 설명 | 위, 작은창자이나 큰창자에서 영양분을 흡수하기 위한 모세혈관조직은 모두 간으로 연결된다. 즉 소화기에 흡수한 영양분이 가득한 피는 모두 간으로 연결되는데 이것을 문맥계라고 한다. |
||
| TGL | triglyceride; triglyceride lipase |
|---|---|
| HTGL | hepatic triglyceride lipase |
| HA | H antigen; Hakim-Adams [syndrome]; halothane anesthesia; Hartley [guinea pig]; headache; health alli... |
| CALP | congenital absence of left pericardium |
| CAV | congenital absence of vagina; congenital adrenal virilism; constant angular velocity; croup-associat... |
| H-TGL | Hepatic triglyceride lipase |
|---|---|
| HL | Hepatic Lipase |
| CAE | Childhood Absence Epilepsy |
| CAVD | Congenital absence of the vas deferens |
| CBAVD | Congenital bilateal absence of the vas deferens |
| high blood triglyceride | <biochemistry> Elevation of triglycerides, a fatty substance found in the bloodstream. Normal triglyceride blood levels should be 10-150 milligrams per decilitre. Elevations of the triglyceride level (particularly in association with elevated cholesterol) have been correlated with the development of atherosclerosis, the underlying cause of heart disease and stroke. Origin: Gr. Haima = blood (27 Sep 1997) |
|---|---|
| triglyceride | <biochemistry> Storage fats of animal adipose tissue where they are largely glycerol esters of saturated fatty acids. Also found in the bloodstream with normal blood levels between 10-150 milligrams per decilitre. Elevations of the triglyceride level (particularly in association with elevated cholesterol) have been correlated with the development of atherosclerosis, the underlying cause of heart disease and stroke. In plants they tend to be esters of unsaturated fatty acids (vegetable oils). Present as a minor component of cell membrane. Important energy supply in heart muscle. (27 Sep 1997) |
| absence | Paroxysmal attacks of impaired consciousness, occasionally accompanied by spasm or twitching of cephalic muscles, which usually can be brought on by hyperventilation; depending on the type and severity of the absence, the EEG may show an abrupt onset of a 3/sec spike and wave pattern as in simple absence, or in atypical cases, a 4/sec spike and wave or faster spike complexes. The clinical states accompanying these EEG abnormalities may be classified as: 1) absence with no overt manifestations, e.g., simple absence; epileptic absence; subclinical absence; 2) absence with clonic movements, e.g., myoclonic absence; 3) absence with atonic states, e.g., atonic absence; 4) absence with tonic contractions, e.g., hypertonic muscular contraction; 5) absence with automatisms, e.g., various stereotyped movements, usually of the face or hands; 6) absence with atypical features, e.g., bizarre motor activity. Origin: L. Absentia (05 Mar 2000) |
| absence seizure | <neurology> A type of seizure that in contrast to the grand mal seizure, are noted for their brevity and for the degree of loss of awareness (brief staring spell) accompanied by minimal motor manifestations. A common form of childhood epilepsy. (06 Oct 1997) |
| Aeromonas hydrophilia lipase-acyltransferase | <enzyme> A member of the lipase family; a distinct group of lipolytic enzymes which have a novel active site structure Registry number: EC 3.1.1.- Synonym: gcat (26 Jun 1999) |
| atypical absence seizure | An absence seizure associated with an EEG pattern of irregular or slow spike and wave at less than 2.5 Hz or paroxysmal fast activity on an abnormally slow background EEG. (05 Mar 2000) |
| childhood absence epilepsy | A generalised epilepsy syndrome characterised by the onset of absence seizures in childhood, typically at age six or seven years. There is a strong genetic predisposition and girls are affected more often than boys. EEG reveals generalised 3 Hz spike-wave activity on a normal background. Prognosis for remission is good if the patient does not also have generalised tonic-clonic seizures. See: absence. Synonym: petit mal epilepsy, pyknolepsy. (05 Mar 2000) |
| congenital absence of pulmonary valve | <radiology> BIG central pulmonary arteries, big RV (12 Dec 1998) |
| pure absence | A brief clouding of consciousness accompanied by the abrupt onset of 3/sec spikes and waves on EEG. Synonym: pure absence. (05 Mar 2000) |
| simple absence | A brief clouding of consciousness accompanied by the abrupt onset of 3/sec spikes and waves on EEG. Synonym: pure absence. (05 Mar 2000) |
| diacylglycerol lipase | <enzyme> An enzyme of the hydrolase class that catalyses the reaction of triacylglycerol and water to yield diacylglycerol and a fatty acid anion. The enzyme hydrolyzes triacylglycerols in chylomicrons, very-low-density lipoproteins, low-density lipoproteins, and diacylglycerols. It occurs on capillary endothelial surfaces, especially in mammary, muscle, and adipose tissue. Genetic deficiency of the enzyme causes familial hyperlipoproteinaemia type I. Chemical name: Triacylglycero-protein acylhydrolase Registry number: EC 3.1.1.34 (12 Dec 1998) |
| diglyceride lipase | <enzyme> An enzyme of the hydrolase class that catalyses the reaction of triacylglycerol and water to yield diacylglycerol and a fatty acid anion. The enzyme hydrolyzes triacylglycerols in chylomicrons, very-low-density lipoproteins, low-density lipoproteins, and diacylglycerols. It occurs on capillary endothelial surfaces, especially in mammary, muscle, and adipose tissue. Genetic deficiency of the enzyme causes familial hyperlipoproteinaemia type I. Chemical name: Triacylglycero-protein acylhydrolase Registry number: EC 3.1.1.34 (12 Dec 1998) |
| epilepsy, absence | Epileptic seizures that consist of a sudden cessation of ongoing conscious activity without convulsive muscular activity or loss of postural control. These seizures may be so brief as to be inapparent, lasting seconds and occasionally several minutes. Absence seizures usually begin in otherwise neurologically normal children and rarely appear for the first time in adults. The seizures may occur hundreds of times per day and go on for weeks or months before it is recognised that a child is having seizures. (12 Dec 1998) |
| juvenile absence epilepsy | A generalised epilepsy syndrome with onset around puberty, characterised by absence seizures and generalised tonic-clonic seizures. EEG often shows a greater than 3 Hz generalised spike wave pattern. (05 Mar 2000) |
| familial lipoprotein lipase deficiency | An rare inherited disorder where there is a deficiency of an enzyme (lipoprotein lipase) which breaks down fat molecules, causing the accumulation of fats or lipoproteins in the blood. Symptoms in infancy include abdominal pain (appears as if its colic), failure to thrive and skin lesions (xanthomas). (27 Sep 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|