| 영문 | uterus | 한글 | 자궁 |
|---|---|---|---|
| 설명 | 포유동물의 암컷에 있는, 중간이 비어있는 근육성기관으로 그 안에서 정상적으로 수정된 난자가 착상하여 그곳에서 발육하는 태아가 영양분을 받는다. 임신되지 않은 사람의 자궁은 서양배모양으로 길이 7~8cm정도로 몸통, 바닥, 잘룩, 목로 구분되어 있다. 내강은 아래로 질에, 위로 양측의 난관에 열려 있고, 질에 직접 접속되고 간접적으로 근처의 여러 가지 골반장기에 의해 지지되어 있다. 자궁의 가장 안쪽을 자궁내막, 중간의 근육층을 자궁근막, 그리고 자궁의 가장 바깥을 싸는 막을 자궁외막이라 한다. |
||
| MPDS | mandibular pain dysfunction syndrome; myofascial pain dysfunction syndrome |
|---|---|
| HFU | hand-foot-uterus [syndrome] |
| POU | placenta, ovary, and uterus |
| AMI | Acute Myocardial Infarction - Complications(Cx) 1. Early ... |
| CREST Syndrome | 1. Calcinosis cutis 2. Raynaud's phenomenon 3. Esophageal ... |
| Di | Dysfunction Index |
|---|---|
| ED | ERECTILE DYSFUNCTION |
| ETD | Eye tracking dysfunction |
| LVD | Left Ventricular Dysfunction |
| LVSD | Left ventricular systolic dysfunction |
| papillary muscle dysfunction | Impaired function of a papillary muscle, usually due to ischemia or infarction, with resulting incompetence of the mitral valve. Synonym: papillary muscle syndrome. (05 Mar 2000) |
|---|---|
| ventricular dysfunction | A condition in which the ventricles of the heart exhibit a decreased functionality. (12 Dec 1998) |
| ventricular dysfunction, left | A condition in which the left ventricle of the heart exhibits a decreased functionality. This decreased function could lead to congestive heart failure or myocardial infarction, among other cardiovascular diseases. Diagnostic measurements that indicate this condition include a diminished ejection fraction and a depressed level of motility of the left ventricular wall. (12 Dec 1998) |
| ventricular dysfunction, right | A condition in which the right ventricle of the heart exhibits a decreased functionality. This decreased function could lead to congestive heart failure or myocardial infarction, among other cardiovascular diseases. Diagnostic measurements that indicate this condition include a diminished ejection fraction and a depressed level of motility of the right ventricular wall. (12 Dec 1998) |
| phagocyte bactericidal dysfunction | Disorders in which phagocytic cells cannot kill ingested bacteria; characterised by frequent recurring infection with formulation of granulomas. (12 Dec 1998) |
| phagocyte dysfunction | Disorder in which the ability of the phagocyte to engulf and ingest particles may be impaired. (05 Mar 2000) |
| phagocytic dysfunction disorders immunodeficiency | Suppression in number or function of phagocytic cells such as in chronic granulomatous disease. Synonym: phagocytic dysfunction disorders immunodeficiency. Origin: L. Phagedaena, Gr Phago, To eat. (05 Mar 2000) |
| phagocytic dysfunction immunodeficiency | Suppression in number or function of phagocytic cells such as in chronic granulomatous disease. Synonym: phagocytic dysfunction disorders immunodeficiency. Origin: L. Phagedaena, Gr Phago, To eat. (05 Mar 2000) |
| minimal brain dysfunction | An inability to control behaviour due to difficulty in processing neural stimuli. (12 Dec 1998) |
| placental dysfunction | 1. Denoting faulty development or ripening; often connoting structural and/or functional abnormalities. 2. In obstetrics, denoting an infant whose birth weight is inappropriately low for its gestational age. 3. Immature development of the placenta so that normal function does not occur. Synonym: placental dysfunction. (05 Mar 2000) |
| placental dysfunction syndrome | <syndrome> Foetal malnutrition and hypoxia resulting from impaired transfer of oxygen and various nutritive materials from mother to foetus. (05 Mar 2000) |
| constitutional hepatic dysfunction | Mild jaundice due to increased amounts of unconjugated bilirubin in the plasma without evidence of liver damage, biliary obstruction, or haemolysis; thought to be due to an inborn error of metabolism in which the excretion of bilirubin by the liver is defective, ascribed to decreased conjugation of bilirubin as a glucuronide or impaired uptake of hepatic bilirubin. Synonym: benign familial icterus, constitutional hepatic dysfunction, Gilbert's disease, Gilbert's syndrome, Hebra's disease. (05 Mar 2000) |
| constitutional liver dysfunction | An inherited disorder that affects the way bilirubin in handled by the liver. Thought to be due to an inborn error of bilirubin metabolism. Symptoms include mild jaundice, weakness, fatigue, nausea and abdominal pain. (27 Sep 1997) |
| myofacial pain-dysfunction syndrome | <syndrome> Dysfunction of the masticatory apparatus related to spasm of the muscles of mastication precipitated by occlusal dysharmony or alteration in vertical dimension of the jaws, and exacerbated by emotional stress; characterised by pain in the preauricular region, muscle tenderness, popping noise in the temporomandibular joint, and limitation of jaw motion. Synonym: temporomandibular joint pain-dysfunction syndrome. (05 Mar 2000) |
| hereditary peroneal nerve dysfunction | <neurology> A slowly progressive genetic disorder characterised by muscle atrophy in the feet and the legs, progressing to the hands and arms, due to a disorder involving the destruction of nerves (degeneration of the myelin sheath). Other features include foot drop and a slapping gait. There is no specific treatment for this disorder. (27 Sep 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|