| HPAFT | hereditary persistence of alfa-fetoprotein |
|---|---|
| HPFH | hereditary persistence of fetal hemoglobin |
| N-P | need-persistence |
| ILD | interstitial lung disease; intraoperative localization device; ischemic leg disease; ischemic limb d... |
| LAC | La Crosse [virus]; lactase; left atrial circumflex [artery]; left atrial contraction; linguoaxiocerv... |
| HPFH | Hereditary Persistence of Fetal Hemoglobin |
|---|---|
| lactase | Beta-galactosidase |
| L | Lactase |
| LPH | Lactase phlorizin hydrolase |
| persistence | 1. The tendency of a cell to continue moving in one direction: an internal bias on the random walk behaviour that cells exhibit in isotropic environments. 2. Of viruses that persist in a cell population, animal, plant or population for long periods often in a nonreplicating form, by such strategies as integration into host DNA, immunological suppression or mutation into forms with slow replication. (18 Nov 1997) |
|---|---|
| hereditary persistence of foetal haemoglobin | <haematology> Hereditary persistence of foetal haemoglobin is a genetic condition where adult types of haemoglobin fail to develop and the types of haemoglobin the individual had as a foetus remains present well past the point when they would normally have stopped being produced. (09 Oct 1997) |
| adult lactase deficiency | Onset of lactase deficiency, with resulting milk intolerance and malabsorption, in adulthood. Inherited forms may not be manifested until adulthood; any process that damages the intestinal lining cells can cause lactase deficiency in adults. (05 Mar 2000) |
| pro-lactase-phlorizin hydrolase | <chemical> Synonym: pro-lph (26 Jun 1999) |
| deficiency, lactase | Lack of the enzyme lactase resulting in failure to digest lactose in milk (lactose intolerance). (12 Dec 1998) |
| lactase | Enzyme that breaks down the milk sugar lactose. (12 Dec 1998) |
| lactase deficiency | An intolerance to milk and dairy products due to a deficiency of lactase in the intestine. Lactase is a enzyme which breaks down milk sugar or lactose. This condition is common in adults and may affect as many as 70-90% of Asians, African Americans, Native Americans and Mediterranean populations. This condition may also develop as the result of an intestinal disease such as celiac sprue. Symptoms include abdominal cramps, bloating, nausea, weight loss and diarrhoea. Treatment involves removing milk products from the diet. For infant's see Lactofree or ProSobee. (27 Sep 1997) |
| lactase restriction | An inherited trait in which there is low lactase activity and thus there is defective lactose intestinal metabolism. Compare: lactase persistence. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|