| familial hyperprebetalipoproteinaemia | Plasma levels of VLDL, pre-beta-lipoproteins and triglycerides are increased on a normal diet, but beta-lipoproteins, cholesterol, and phospholipids are normal; hypertriglyceridemia is induced by a high carbohydrate diet; may be accompanied by abnormal glucose tolerance and susceptibility to ischemic heart disease; probably autosomal recessive inheritance. Synonym: carbohydrate-induced hyperlipaemia, familial hyperprebetalipoproteinaemia, familial hypertriglyceridemia. (05 Mar 2000) |
|---|---|
| familial hypertriglyceridaemia | <biochemistry> A common inherited disorder in which the concentration of VLDL is elevated in the bloodstream. VLDL is the lipoprotein carrier that carries triglycerides. 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. (27 Sep 1997) |
| 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) |
| familial hypertrophic cardiomyopathy | Familial occurrence of hypertrophic cardiomyopathy exhibiting an autosomal dominant pattern of inheritance. Familial cardiomyopathy of various kinds occurs with autosomal dominant inheritance. There is also an asymmetrical form affecting the ventricles and the interventricular septum. (05 Mar 2000) |
| familial hypobetalipoproteinaemia | A disorder similar to abetalipoproteinaemia; chylomicron formation still occurs, but LDL levels are typically low. (05 Mar 2000) |
| familial hypogonadotropic hypogonadism | A group of disorders characterised by failure of sexual development, owing to inadequate secretion of pituitary gonadotropins; perhaps X-linked or autosomal recessive inheritance. (05 Mar 2000) |
| familial hypophosphatemic rickets | <radiology> X-linked recessive, defect in renal tubular resorption of phosphate, presents at 1 yr, progressive limb deformities X-ray: less severe changes than other rickets, presents later Differential diagnosis features: family hx, normal serum calcium, marked hypophosphataemia (decreased PO4), no secondary hyperparathyroidism (12 Dec 1998) |
| familial hypoplastic anaemia | Congenital nonregenerative, familial hypoplastic, or pure red cell anaemia; erythrogenesis imperfecta; Diamond-Blackfan syndrome; autosomal recessive normocytic normochromic anaemia resulting from congenital hypoplasia of the bone marrow, which is grossly deficient in erythroid precursors while other elements are normal; anaemia is progressive and severe, but leukocyte and platelet counts are normal or slightly reduced; survival of transfused erythrocytes is normal; minor congenital anomalies are found in some patients. Synonym: congenital nonregenerative anaemia, Diamond-Blackfan anaemia, Diamond-Blackfan syndrome, erythrogenesis imperfecta, familial hypoplastic anaemia, pure red cell anaemia. (05 Mar 2000) |
| familial intestinal polyposis | Begins usually in late childhood; polyps increase in numbers, causing symptoms of chronic colitis, and carcinoma of the colon almost invariably develops in untreated cases; autosomal dominant inheritance. In the Gardner syndrome there are extracolonic changes (desmoid tumours, etc.). Synonym: polyposis coli. Hamartomatous polyposis of the small or large intestine, Peutz-Jeghers syndrome with melanin spots on the lips, less common, miscellaneous, rare, and doubtful occurrences. Synonym: familial intestinal polyposis. (05 Mar 2000) |
| familial juvenile nephrophthisis | <nephrology> A rare hereditary kidney disease characterised by the gradual loss of kidney function due to the presence of cysts in the renal medulla. Symptoms include high urine output (cannot concentrate the urine), weakness, weight loss, nocturia, fatigue and headache. There is no cure and usually progresses from chronic renal failure to end stage renal disease. (27 Sep 1997) |
| familial lipodystrophy | Autosomal dominant; partial lip associated with multifacial hypoplasin, retarded bone age, and hypotichosis. (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) |
| familial lipoprotein lipase inhibitor | An inhibitor found in certain individuals that inhibits lipoprotein lipase resulting in accumulation of chylomicrons, VLDL, and triacylglycerols; similar in symptoms to familial lipoprotein lipase deficiency. (05 Mar 2000) |
| familial mediterranean fever | An inherited intestinal disorder that is characterised by recurrent fevers and intestinal inflammation. Usually has onset between the ages of 5 and 15 years and is more common in those of Mediterranean descent. Symptoms include fevers and abdominal pain. Some may also suffer from chest pains, multiple joint pains and red swollen legs. (27 Sep 1997) |
| familial mental retardation 1 | See FMR1. (12 Dec 1998) |
Synonyms : Therapy, Family, Family Therapies, Therapies, Family
Synonyms : Famotidine Hydrochloride, MK-208, Pepcid, YM-11170, MK 208, MK208, YM 11170, YM11170
Synonyms : Famous Person, Person, Famous, Persons, Famous
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|---|---|---|---|
|
서울파모티딘정20mg - 새창
|
서울제약 |
A37001181 | Famotidine | 전문의약품 | 급여 |
|
한서파모티딘정20mg - 새창
|
한서제약 |
A03601081 | Famotidine | 전문의약품 | 급여 |
|
파마겐정 - 새창
|
일화 |
A06501181 | Famotidine | 전문의약품 | 급여 |
|
팜틴정20mg - 새창
|
신풍제약 |
A00302221 | Famotidine | 전문의약품 | 급여 |
|
베모딘정20mg - 새창
|
헤파가드 |
A57050131 | Famotidine | 전문의약품 | 삭제 |
|
모틴정20mg - 새창
|
명인제약 |
A09201141 | Famotidine | 전문의약품 | 삭제 |
|
스파딘정20mg - 새창
|
진양제약 |
A10701121 | Famotidine | 전문의약품 | 급여 |
|
파포틴정 - 새창
|
바이넥스 |
A04801971 | Famotidine | 전문의약품 | 급여 |
|
화이티딘정20mg - 새창
|
한일약품공업 |
A01002591 | Famotidine | 전문의약품 | 삭제 |
|
페로틴정 - 새창
|
코오롱제약 |
A04703381 | Famotidine | 전문의약품 | 급여 |
| famotidine |
a histamine blocker (trade name Pepcid) used to treat peptic ulcers and gastritis and esophageal reflux
출처: wordnet.princeton.edu/perl/webwn
|
|---|---|
| familial intestinal polyposis |
familial adenomatous p.
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
|
| familial hypophosphatemic osteomalacia |
osteomalacia occurring in familial hypophosphatemic rickets.
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
|
| family |
Scientific classification or biological classification is how biologists group and categorize extinct and living species of organisms. Modern classification has its roots in the system of Carolus Linnaeus, who grouped species according to shared physical characteristics. These groupings have been revised since Linnaeus to improve consistency with the Darwinian principle of common descent. ...
출처: en.wikipedia.org/wiki/Family(biology)
|
| family |
In mathematics, a family is a collection. It is a formal version of a lookup table. It consists of a set, called the index set, containing the keys, and a mapping from those keys onto the elements of the family. Each key points to exactly one element of the family and each element belongs to at least one key. As different keys may point to the same element, a family can, unlike a set, contain the same element several times. ...
출처: en.wikipedia.org/wiki/Family_(mathematics)
|
| FAM | personal knowledge or information about someone or something |
|---|---|
| FAM | the experience of becoming familiar with something |
| FAM | make familiar or acquainted with |
| FAM | make familiar or acquainted |
| FAM | having achieved a comfortable relationship with your environment |
| FAM | serving to make familiar |
| FAM | in an intimately familiar manner |
| FAM | primary social group |
| FAM | people descended from a common ancestor |
| FAM | a collection of things sharing a common attribute |
| FAM | a social unit living together |
| FAM | (biology) a taxonomic group containing one or more genera |
