| 영문 | testicular feminization syndrome | 한글 | 고환여성화증후군 |
|---|---|---|---|
| 설명 | 이차성장을 포함하여, 외성기의 발육은 여성이지만 고환이 존재하고, 자궁과 자궁관이 결핍되어 있는 남성 거짓남녀한몸증의 극단적 형태이다. 이것은 테스토스테론의 작용에 대한 말단기관의 저항에 기인한다. |
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| AFP | Alpha(α) Feto-Protein [HP 1826, 1858, 1859, 2265] ; Oncofetal Antigens &nbs... |
|---|---|
| TFM | testicular feminization male; testicular feminization mutation; total fluid movement; transmission e... |
| MPDS | mandibular pain dysfunction syndrome; myofascial pain dysfunction syndrome |
| AIS | Androgen Insensitive Syndrome = Testicular Feminization Syndrome |
| TDF | Testicular-Determining Factor = HY Factor |
| DRO | Differential Reinforcement of Other Behaviour |
|---|---|
| MOTT | Mycobacteria Other Than Tuberculosis |
| OND | Other Neurological Diseases |
| SO | significant other |
| AOD | and other drug |
| other-directed | Pertaining to a person readily influenced by the attitudes of others. (05 Mar 2000) |
|---|---|
| transferases (other substituted phosphate groups) | <enzyme> A class of enzymes that transfers substituted phosphate groups. Registry number: EC 2.7.8 (12 Dec 1998) |
| 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) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|