| FHTG | familial hypertriglyceridemia |
|---|---|
| HTG | hypertriglyceridemia |
| FHH | Familial Hypocalciuric Hypercalcemia = Familial Benign Hypercalcemia |
| FAD | familial Alzheimer dementia; familial autonomic dysfunction; fetal activity-acceleration determinati... |
| FAP | familial adenomatous polyposis; familial amyloid polyneuropathy; fatty acid polyunsaturated; fatty a... |
| BaEV | Baboon endogenous virus |
|---|---|
| EDLF | Endogenous digitalis-like factor |
| EDLS | Endogenous digitalis-like substance |
| EGP | Endogenous glucose production |
| EOP | Endogenous opioid peptide |
| familial hypertriglyceridemia | Hyperlipoproteinaemia characterised by the presence of large amounts of chylomicrons and triglycerides in the plasma when the patient has a normal diet, and their disappearance on a fat-free diet; low alpha-and beta-lipoproteins on a normal diet, with increase on fat-free diet; decreased plasma postheparin lipolytic activity; and low tissue lipoprotein lipase activity. It is accompanied by bouts of abdominal pain, hepatosplenomegaly, pancreatitis, and eruptive xanthomas; autosomal recessive inheritance. See: familial lipoprotein lipase inhibitor. Synonym: Burger-Grutz syndrome, familial fat-induced hyperlipaemia, familial hyperchylomicronaemia, familial hypertriglyceridemia, idiopathic hyperlipaemia. (05 Mar 2000) |
|---|---|
| hypertriglyceridemia | Condition of elevated triglyceride concentration in the blood; an inherited form occurs in familial hyperlipoproteinaemia IIb and hyperlipoproteinaemia type IV. It has been linked to higher risk of heart disease and arteriosclerosis. (12 Dec 1998) |
| endogenous | <biology> Developing or originating within the organisms or arising from causes within the organism. Origin: Gr. Gennan = to produce (18 Nov 1997) |
| endogenous creatinine clearance | A term distinguishing measurements based on the creatinine normally present in plasma; since no infusion is necessary, an average value may be obtained by collecting urine for a long period, e.g., 24 hours. (05 Mar 2000) |
| endogenous cycle | The portion of a parasitic life cycle occurring within the host. (05 Mar 2000) |
| endogenous depression | <psychiatry> A clinical syndrome that includes a persistent sad mood or loss of interest in activities that persists for at least 2 weeks in the absence of external precipitants. This should not be confused with a grief reaction (death of loved one). Features may include change in eating habits, insomnia, early morning wakening, lack of interest, depressed mood, fatigue and suicidal thoughts. (27 Sep 1997) |
| endogenous fibres | Nerve fibre's interconnecting subdivisions of the cerebral cortex of the same hemisphere or different segments of the spinal cord on the same side. Synonym: endogenous fibres, intrinsic fibres. (05 Mar 2000) |
| endogenous infection | Infection caused by an infectious agent already present in the body, the previous infection having been inapparent. (05 Mar 2000) |
| endogenous pyrogen | Fever producing substance released by leucocytes (and Kuppfer cells in particular) that acts on the hypothalamic thermoregulatory centre. Now known to be interleukin-1. (18 Nov 1997) |
| endogenous retrovirus | <virology> A retrovirus that has become dormant and exists as DNA copies in every cell in the body of its host and is passed down from generation to generation. (09 Oct 1997) |
| endogenous virus | <virology> A virus with the ability to integrate into the genome of its host and become dormant, so that it exists as DNA copies in every cell in the body of the host and is passed down from generation to generation. A virus that causes a persistent infection. (09 Oct 1997) |
| benign familial chorea | A rare, nonprogressive movement disorder characterised by chorea and athetosis appearing in early childhood, most commonly manifested as gait ataxia and upper limb coordination. Intellect is unaffected. Probably autosomal-dominance inheritance with incomplete penetrance. (05 Mar 2000) |
| benign familial chronic pemphigus | Recurrent eruption of vesicles and bullae that become scaling and crusted lesions with vesicular borders, predominantly of the neck, groin, and axillary regions; autosomal dominant inheritance, presenting in late adolescence or early adult life. Synonym: Hailey-Hailey disease. (05 Mar 2000) |
| benign familial icterus | Mild jaundice due to increased amounts of unconjugated bilirubin in the plasma without evidence of liver damage, biliary obstruction, or haemolysis; thought to be due to an inborn error of metabolism in which the excretion of bilirubin by the liver is defective, ascribed to decreased conjugation of bilirubin as a glucuronide or impaired uptake of hepatic bilirubin. Synonym: benign familial icterus, constitutional hepatic dysfunction, Gilbert's disease, Gilbert's syndrome, Hebra's disease. (05 Mar 2000) |
| cancer, breast, familial | A number of factors have been identified that increase the risk of breast cancer. One of the strongest of these risk factors is the history of breast cancer in a relative. About 15-20% of women with breast cancer have such a family history of the disease, clearly reflecting the participation of inherited (genetic) components in the development of some breast cancers. Dominant breast cancer suceptibility genes, including BRCA1 and BRCA2, appear responsible for about 5% of all breast cancer. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|