| 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... |
| APO | abductor pollicis obliguus; acquired pendular oscillation; adriamycin, prednisone, vincristine; adve... |
| Apo, apo | apolipoprotein |
| FDB | Familial Defective Apolipoprotein B-100 |
|---|---|
| APO E | Apolipoprotein E |
| APO | Apolipoprotein |
| APOE | Apolipoprotein |
| a | Apolipoprotein |
familial leiomyomatosis cutis et uteri (가족성 피부 자궁 근종증
| apolipoprotein | <biochemistry, protein> The protein component of serum lipoproteins. Small proteins containing multiple copies of the kringle domain. (18 Nov 1997) |
|---|---|
| apolipoprotein A-I | <biochemistry> The major protein component of high density lipoproteins. It is instrumental in promoting efflux of cholesterol from extrahepatic tissue to the liver where it is metabolised and excreted from the body. The compound is the activator of lecithin-cholesterol acyltransferase which forms cholesteryl esters in hdl. The gene for this apolipoprotein is found on the long arm of chromosome 11. (12 Dec 1998) |
| apolipoprotein A-II | <biochemistry> A component of high density lipoproteins. It is instrumental in promoting efflux of cholesterol from extrahepatic tissue to the liver where it is metabolised and excreted from the body. This protein modulates the activation of lecithin-cholesterol acyltransferase in the presence of apolipoprotein A-I. (12 Dec 1998) |
| apolipoprotein A-IV | <biochemistry> An apolipoprotein secreted with chylomicrons. (05 Mar 2000) |
| apolipoprotein B | <biochemistry> Apolipoproteins found in LDL, VLDL, and IDL. Elevated in the plasma of individuals with familial hyperlipoproteinaemia. (05 Mar 2000) |
| apolipoprotein B-100 | <biochemistry> An apolipoprotein found in LDL, VLDL, and IDL. The ligand for the LDL receptor; absent in certain types of abetalipoproteinaemia. Apolipoproteins are proteins on the surface of the lipoprotein complex that bind to specific enzymes or transport proteins across the cell membrane. The normal range is 40 to 125 mg/dl. Elevated levels may be seen in familial combined hyperlipidaemia and acquired hyperlipidaemia. Elevation may also be seen in cases of acute angina and myocardial infarction. (27 Sep 1997) |
| apolipoprotein B-48 | <biochemistry> An apolipoprotein found in chylomicrons and chylomicron remnants. Retained in intestine of individuals with chylomicron retention disease. (05 Mar 2000) |
| apolipoprotein C-I | <biochemistry> An apolipoprotein found in VLDL, HDL, and chylomicrons. (05 Mar 2000) |
| apolipoprotein C-II | <biochemistry> An apolipoprotein found in VLDL, HDL, and chylomicrons; an activator of lipoprotein lipase; a deficiency will result in accumulation of chylomicrons and triacylglycerols. Apolipoproteins are proteins on the surface of the lipoprotein complex that bind to specific enzymes or transport proteins across the cell membrane. Elevated levels may be seen in acute angina and acute myocardial infarction. Low levels are seen in apolipoprotein C-II deficiency. Normal levels are seen in type I hyperlipoproteinaemia. (27 Sep 1997) |
| apolipoprotein C-III | <biochemistry> An apolipoprotein found in VLDL, HDL, and chylomicrons. (05 Mar 2000) |
| apolipoprotein D | <biochemistry> An apolipoprotein found in HDL whose function is unclear. (05 Mar 2000) |
| apolipoprotein E | <biochemistry> An apolipoprotein found in VLDL, HDL, chylomicrons, and chylomicron remnants. Elevated in individuals with type III hyperlipoproteinaemia. (05 Mar 2000) |
| apolipoprotein N-acyltransferase | <enzyme> From e. Coli; catalyses the conversion of apolipoprotein to mature lipoprotein Registry number: EC 2.3.1.- Synonym: alp n-acyltransferase (26 Jun 1999) |
| 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) |
Synonyms : Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type, Apolipoprotein B Deficiency Disease, Hypobetalipoproteinemia, Familial, Apo B, Apolipoprotein B Deficiencies
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|