| 영문 | hypophysis, pituitary | 한글 | 뇌하수체 |
|---|---|---|---|
| 설명 | 뇌바닥부에 있으며 터어키안장에 위치하는 이중기원의 상피성 소체. 중요한 내분비 장기 중 하나이다. 전엽, 중엽, 후엽의 세 부분으로 이루어져 있고, 다른 내분비선의 활동을 지배하는 호르몬을 분비하며, 생식과 발육에 밀접한 관계가 있다. |
||
| 영문 | specific gravity | 한글 | 비중 |
|---|---|---|---|
| 설명 | 단위 부피당 질량. 소변의 비중은 소변의 농도를 반영한다. 예를 들어 소변의 비중이 크면, 콩팥의 물흡수가 원활히 이루어지고 있음을 나타낸다. |
||
| ASD | aldosterone secretion defect; Alzheimer senile dementia; antisiphon device; arthritis syphilitica de... |
|---|---|
| IASD | interatrial septal defect; inter-auricular septal defect |
| SD | Sandhoff disease; senile dementia; septal defect; serologically defined; serologically detectable; s... |
| HBsAg/adr | hepatitis B surface antigen manifesting group-specific determinant a and subtype-specific determinan... |
| LSP | left sacroposterior [fetal position]; linguistic string project; liver-specific protein; lymphocyte-... |
| ASD | Atrial septal defect |
|---|---|
| CHD | Congenital heart defect |
| CSD | critical size defect |
| LPD | Luteal phase defect |
| MD | Mean Defect |
| site-specific DNA-methyltransferase (adenine-specific) | <enzyme> An enzyme responsible for producing a species-characteristic methylation pattern on adenine residues in a specific short base sequence in the host cell DNA. The enzyme catalyses the methylation of DNA adenine in the presence of s-adenosyl-l-methionine to form DNA containing 6-methylaminopurine and s-adenosyl-l-homocysteine. Registry number: EC 2.1.1.72 (12 Dec 1998) |
|---|---|
| site-specific DNA methyltransferase (cytosine-specific) | <enzyme> An enzyme responsible for producing a species-characteristic methylation pattern on cytosine residues in a specific short base sequence in the host cell's DNA. The enzyme catalyses the methylation of DNA cytosine in the presence of s-adenosyl-l-methionine to form s-adenosyl-l-homocysteine and DNA containing 5-methylcytosine. Registry number: EC 2.1.1.73 (12 Dec 1998) |
| acquired platelet function defect | <haematology> Platelet function can be affected by a number of different disease processes including polycythaemia vera, leukaemia, myelofibrosis, renal failure, multiple myeloma and some medications (for example penicillins, salicylates, phenothiazines). Disturbed blood clotting can be manifested by: easy bruising, bleeding gums, nosebleeds, abnormal vaginal bleeding, rectal bleeding, skin rash, vomiting blood, coughing up blood or blood in the urine. A measure of bleeding time and coagulation profile will be part of the evaluation. (29 Dec 1997) |
| aortic septal defect | A small congenital opening between the aorta and pulmonary artery about 1 cm above the semilunar valves, e.g., aorticopulmonary window. Synonym: aorticopulmonary window. (05 Mar 2000) |
| aortopulmonary septal defect | A congenital anomaly in which there is abnormal communication between the ascending aorta and pulmonary artery just above the semilunar valves. (12 Dec 1998) |
| atrial septal defect | <cardiology> An inherited condition where there is nonclosure of the foramen ovale at birth, resulting in congenital heart disease. Usually asymptomatic until the third or fourth decades of life. Symptoms include exertional shortness of breath, fatigue and palpitations. Acronym: ASD (12 Jan 1998) |
| atrial ventricular canal defect | A defect caused by deficient or absent septal tissue immediately above and below the normal level of the atrioventricular valves, including the region normally occupied by the A-V septum in hearts with two ventricles. The A-V valves are abnormal to a varying degree. (05 Mar 2000) |
| birth defect | Defect present at birth; sometimes referred to as congenital defect. (05 Mar 2000) |
| ventricular septal defect | <cardiology, embryology> A congenital heart defect where an abnormal opening exists in the ventricular septum. Blood flows from the higher pressure left ventricle (through the defect) into the right ventricle. (12 Jan 1998) |
| Gerbode defect | <cardiology, embryology> A defect in the interventricular portion of the membranous septum, associated with a communication between the right ventricle and the right atrium through an abnormality in the tricuspid valve. (05 Mar 2000) |
| mass defect | <chemistry, radiobiology> Of a nucleus, the difference between the sum of the masses of the constituent nucleons and the mass of the nucleus. (16 Dec 1997) |
| partial endocardial cushion defect | <radiology> Incomplete endocardial cushion defect components: ostium primum atrial septal defect, cleft in anterior mitral valve findings: right AV valve is usually normal, with or without mitral insufficiency, communication between LA_RA or LV-RA, occasionally LV-RV Cf: complete endocardial cushion defect (12 Dec 1998) |
| relative afferent pupillary defect | An asymmetry of the pupillomotor input between the two eyes; tested by alternating the light from one eye to the other and comparing the direct light reactions. (05 Mar 2000) |
| metaphysial fibrous cortical defect | A small (less than 2 to 3 cm in diameter) fibrous cortical d. (05 Mar 2000) |
| complete endocardial cushion defect | <radiology> Arteriovenous canal components: low atrial septal defect (ostium primum), high VSD, cleft anterior leaflet of mitral valve, cleft septal leaflet of tricuspid valve, one AV valve common to RV and LV with 5-6 leaflets findings: 4-chamber enlargement (R greater than L), mitral insufficiency, associated with congestive heart failure and Eisenmenger syndrome, gooseneck deformity on angiogram (elongation and narrowing of the LV outflow tract during diastole) see also: endocardial cushion defect, partial endocardial cushion defect (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|