| familial dysbetalipoproteinaemia | <biochemistry, cardiology> An inherited disorder (gene defect) where both cholesterol and triglycerides are elevated in the same patient. This condition accelerates the effects of atherosclerosis and thus increases the risk of cardiovascular disease. Conditions such as hypothyroidism, obesity and diabetes enhances this risk. Origin: Gr. Haima = blood (27 Sep 1997) |
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| familial emphysema | Emphysema inherited in association with severe alpha-1 antitrypsin deficiency. It may occur as an isolated feature or with cutis laxa and haemolytic anaemia. (05 Mar 2000) |
| familial erythroblastic anaemia | An outmoded term for thalassaemia major. (05 Mar 2000) |
| familial fat-induced hyperlipaemia | 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 glycinuria | A metabolic disorder believed to be due to defective renal glycine reabsorption; it may or may not be accompanied by oxalate urolithiasis; may be the heterozygous state of iminoglycinuria; autosomal dominant inheritance. (05 Mar 2000) |
| familial goiter | A group of heritable thyroid disorders in which goiter is commonly apparent first during childhood; often associated with skeletal and/or mental retardation, and with other signs of hypothyroidism that may develop with age. Various types of familial goiter have been identified: 1) iodide transport defect, in which the gland is unable to concentrate iodide; 2) organification defect, in which the iodination of tyrosine is defective; 3) Pendred's syndrome; 4) coupling defect, in which cretinism results from defective coupling of iodotyrosines to form iodothyronines; 5) iodotyrosine deiodinase defect, in which deiodination of iodotyrosine is defective, considerable glandular loss of these hormonal precursors occurs, and cretinism may be present; 6) plasma iodoprotein disorder, in which an abnormal iodinated serum protein that is insoluble in acidic butanol is present; 7) hereditary hyperthyroidism. (05 Mar 2000) |
| familial high density lipoprotein deficiency | Familial high {density lipoprotein deficiency}; a heritable disorder of lipid metabolism characterised by almost complete absence from plasma of high density lipoproteins, and by storage of cholesterol esters in foam cells, tonsillar enlargement, an orange or yellow-gray colour of the pharyngeal and rectal mucosa, hepatosplenomegaly, lymph node enlargement, corneal opacity, and peripheral neuropathy; autosomal recessive inheritance. Synonym: familial high {density lipoprotein deficiency}, Tangier disease. Origin: G. An-, priv., + alpha, a, + lipoprotein + -aemia, blood (05 Mar 2000) |
| familial hyperbetalipoproteinaemia | Hyperlipoproteinaemia characterised by increased plasma levels of beta-lipoproteins, cholesterol, and phospholipids, but normal triglycerides; heterozygotes have mild lipid changes and are susceptible to atherosclerosis in middle age, but homozygotes have severe changes often with generalised xanthomatosis and xanthelasma, and frank clinical atherosclerosis as young adults. The primary defect is a deficiency of apoprotein of VLDL, and the disorder is divided into two classes: 1) type IIA, which has elevated LDL due to a deficiency of the receptor or a modified apolipoprotein B-100; 2) type IIB, which has elevated LDL and triglycerides; autosomal dominant inheritance. Synonym: familial hyperbetalipoproteinaemia, familial hypercholesteraemic xanthomatosis, familial hypercholesterolaemia. (05 Mar 2000) |
| familial hyperbetalipoproteinaemia and hyperprebetalipoproteinaemia | Hyperlipoproteinaemia characterised by increased plasma levels of LDL, beta-lipoproteins, pre-beta-lipoproteins, cholesterol, phospholipids, and triglycerides; hypertriglyceridemia induced by a high carbohydrate diet, and glucose tolerance is abnormal; frequent eruptive xanthomas and atheromatosis, particularly coronary artery disease; biochemical defect lies in apolipoproteins; there are many varieties. Synonym: carbohydrate-induced hyperlipaemia, dysbetalipoproteinaemia, familial hyperbetalipoproteinaemia and hyperprebetalipoproteinaemia, familial hypercholesterolaemia with hyperlipaemia. (05 Mar 2000) |
| familial hypercholesteraemic xanthomatosis | Hyperlipoproteinaemia characterised by increased plasma levels of beta-lipoproteins, cholesterol, and phospholipids, but normal triglycerides; heterozygotes have mild lipid changes and are susceptible to atherosclerosis in middle age, but homozygotes have severe changes often with generalised xanthomatosis and xanthelasma, and frank clinical atherosclerosis as young adults. The primary defect is a deficiency of apoprotein of VLDL, and the disorder is divided into two classes: 1) type IIA, which has elevated LDL due to a deficiency of the receptor or a modified apolipoprotein B-100; 2) type IIB, which has elevated LDL and triglycerides; autosomal dominant inheritance. Synonym: familial hyperbetalipoproteinaemia, familial hypercholesteraemic xanthomatosis, familial hypercholesterolaemia. (05 Mar 2000) |
| familial hypercholesterolaemia | <biochemistry, cardiology> Excess of cholesterol in plasma as a result of defects in the recycling process that leads to reduced uptake of LDL (low density lipoprotein) into coated vesicles. (18 Nov 1997) |
| familial hypercholesterolaemia with hyperlipaemia | Hyperlipoproteinaemia characterised by increased plasma levels of LDL, beta-lipoproteins, pre-beta-lipoproteins, cholesterol, phospholipids, and triglycerides; hypertriglyceridemia induced by a high carbohydrate diet, and glucose tolerance is abnormal; frequent eruptive xanthomas and atheromatosis, particularly coronary artery disease; biochemical defect lies in apolipoproteins; there are many varieties. Synonym: carbohydrate-induced hyperlipaemia, dysbetalipoproteinaemia, familial hyperbetalipoproteinaemia and hyperprebetalipoproteinaemia, familial hypercholesterolaemia with hyperlipaemia. (05 Mar 2000) |
| familial hyperchylomicronaemia | 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 hyperchylomicronaemia with hyperprebetalipoproteinaemia | Hyperlipoproteinaemia characterised by increased plasma levels of chylomicrons, VLDL, pre-beta-lipoproteins, and triglycerides, and slight rise of cholesterol on a normal diet, with beta-lipoproteins normal; may be accompanied by bouts of abdominal pain, hepatosplenomegaly, susceptibility to atherosclerosis, and abnormal glucose tolerance; probably autosomal recessive inheritance. Synonym: combined fat-and carbohydrate-induced hyperlipaemia, familial hyperchylomicronaemia with hyperprebetalipoproteinaemia, mixed hyperlipaemia. (05 Mar 2000) |
| familial hyperlipoproteinaemia | <biochemistry> A relatively rare (7 out of 1,000) genetic disease in which there is elevation in the blood triglycerides, cholesterol and low density lipoprotein (LDL). Also called type II hyperlipoproteinaemia, familial hyperlipoproteinaemia or familial hypercholesterolaemia. Origin: Gr. Haima = blood (27 Sep 1997) |
Synonyms : Family-Centered Nursing, Family Centered Nursing, Family Nursings, Family-Centered Nursings, Nursing, Family, Nursing, Family-Centered, Nursings, Family, Nursings, Family-Centered
Synonyms : Antinatalist Policy, Family Policy, One Child Policy, One-Child Policy, Pronatalist Policy, Antinatalist Policies, Family Planning Policies, Family Policies, One Child Policies, One-Child Policies, Policies, Antinatalist, Policies, Family, Policies, One Child
Synonyms : Family Planning Programs, Planned Pregnancy, Pregnancy, Planned, Family Planning Program, Family Planning Service, Planned Pregnancies, Planning Service, Family, Planning Services, Family, Pregnancies, Planned, Program, Family Planning, Programs, Family Planning
Synonyms : Family Practices, General Practices, Practice, Family, Practice, General, Practices, Family, Practices, General
Synonyms : Family Relationships, Family Relation, Relation, Family, Relations, Family
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|---|---|---|---|
|
영풍파모티딘정 - 새창
|
영풍제약 |
A25001581 | Famotidine | 전문의약품 | 급여 |
|
동인당파모티딘정 - 새창
|
동인당제약 |
A17200491 | Famotidine | 전문의약품 | 삭제 |
|
한국유나이티드파모티딘정20mg - 새창
|
한국유나이티드제약 |
A12902031 | Famotidine | 전문의약품 | 급여 |
|
파로틴정20mg - 새창
|
대우약품공업 |
A05401921 | Famotidine | 전문의약품 | 삭제 |
|
위더스파모티딘정20mg - 새창
|
위더스메디팜 |
A03700711 | Famotidine | 전문의약품 | 급여 |
|
로카시드정 - 새창
|
한국슈넬제약 |
A07102321 | Famotidine | 전문의약품 | 급여 |
|
폰티나정20mg - 새창
|
국제약품공업 |
A03003231 | Famotidine | 전문의약품 | 삭제 |
|
옥소틴정20mg - 새창
|
알파제약 |
A23502521 | Famotidine | 전문의약품 | 삭제 |
|
신일파모티딘정20mg - 새창
|
신일제약 |
A20702871 | Famotidine | 전문의약품 | 급여 |
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미래파모티딘정20mg - 새창
|
미래제약 |
A20601111 | Famotidine | 전문의약품 | 삭제 |
| family medicine |
family practice: medical practice that provides health care regardless of age or sex while placing emphasis on the family unit
출처: wordnet.princeton.edu/perl/webwn
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| family planning |
birth control: limiting the number of children born
출처: wordnet.princeton.edu/perl/webwn
|
| family practice |
medical practice that provides health care regardless of age or sex while placing emphasis on the family unit
출처: wordnet.princeton.edu/perl/webwn
|
| family therapy |
any of several therapeutic approaches in which a family is treated as a whole
출처: wordnet.princeton.edu/perl/webwn
|
| famine |
dearth: an acute insufficiency a severe shortage of food (as through crop failure) resulting in violent hunger and starvation and death
출처: wordnet.princeton.edu/perl/webwn
|
| FAM | (usually followed by `with') well informed about or knowing thoroughly |
|---|---|
| FAM | a spirit (usually in animal form) that acts as an assistant to a witch or wizard |
| FAM | having fair knowledge of |
| 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 | an act of undue intimacy |
| FAM | close or warm friendship |
| FAM | usualness by virtue of being familiar or well known |
| FAM | a casual manner |
