| ¿µ¹® | acquired immunodeficiency syndrome | ÇÑ±Û | ÈÄõ¸é¿ª°áÇÌÁõÈıº, ¿¡ÀÌÁî |
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| PH | parathyroid hormone; partial hepatectomy; partial hysterectomy; passive hemagglutination; past histo... |
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| SAIDS | sexually acquired immunodeficiency syndrome; simian acquired immune deficiency syndrome |
| AIDS | Acquired Immuno(Immune)-Deficiency Syndrome; ÈÄõ¼º ¸é¿ª °áÇÌ ÁõÈıº |
| AISA | Acquired Idiopathic Sideroblastic Anemia = RARS |
| AAA | abdominal aortic aneurysm/aneurysmectomy; acne-associated arthritis; acquired aplastic anemia; acute... |
| PH | Primary hyperoxaluria |
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| PH1 | Primary hyperoxaluria Type 1 |
| ABI | Acquired Brain Injury |
| AISA | Acquired Idiopathic Sideroblastic Anemia |
| AIDS | Acquired Immune Deficiency Disease Syndrome |
| primary hyperoxaluria and oxalosis | A metabolic disorder characterised by calcium oxalate nephrocalcinosis and nephrolithiasis, extrarenal oxalosis, and increased urinary output of oxalic and glycolic acids; usually evident clinically in the first decade of life, with progressive renal failure and uraemia; autosomal recessive inheritance. Type I is due to an alteration in alanine:glyoxylate aminotransferase; type II is due to an alteration in d-glycerate dehydrogenase. (05 Mar 2000) |
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| hyperoxaluria | A genetic disease of autosomal recessive inheritance that results in the deposition of calcium oxalate in the genitourinary system and kidneys (nephrocalcinosis). Usually evident in the first decade of life, progressive renal failure is not uncommon. Inheritance: autosomal recessive. Origin: Gr. Ouron = urine (27 Sep 1997) |
| hyperoxaluria, primary | Either of two genetic disorders characterised by urinary excretion of large amounts of oxalate, with nephrolithiasis, nephrocalcinosis, early onset of renal failure, and often a generalised deposit of calcium oxalate, resulting from a defect in glyoxalate metabolism. (12 Dec 1998) |
| acquired | In medicine, the word acquired means new or added. New in the sense that it is not genetic (inherited) and added in the sense that is was not congenital (present at birth) but came along later. For example, AIDS is an acquired, not a genetic form of immune deficiency. (12 Dec 1998) |
| acquired agammaglobulinaemia | Heterogeneous group of immunodeficiency syndromes characterised by hypogammaglobulinaemia of most isotypes, variable B-cell defects, and the presence of recurrent bacterial infections. (12 Dec 1998) |
| acquired bronchiectasis | <chest medicine> Persistent and progressive dilation of bronchi or bronchioles as a consequence of inflammatory disease (lung infections), obstruction (tumour) or congenital abnormality (for example cystic fibrosis). Symptoms include fetid breath and paroxysmal coughing, with the expectoration of mucopurulent matter. It may affect the bronchioles uniformly (cylindric bronchiectasis) or occur in irregular pockets (sacculated bronchiectasis) or the dilated bronchi may have terminal bulbous enlargements (fusiform bronchiectasis). Although rarely congenital, it is most often an acquired condition in childhood. (13 Nov 1997) |
| acquired centric relation | See: centric jaw relation. (05 Mar 2000) |
| acquired character | A character developed in a plant or animal as a result of environmental influences during the individual's life. (05 Mar 2000) |
| acquired cuticle | A thin film (about 1 um), derived mainly from salivary glycoproteins, which forms over the surface of a cleansed tooth crown when it is exposed to the saliva. Synonym: acquired cuticle, acquired enamel cuticle, brown pellicle, posteruption cuticle. (05 Mar 2000) |
| acquired drives | Those drives not directly related to biological needs; a secondary drive can be learned as an offshoot of a primary drive, in which case it is often referred to as a motive. Synonym: acquired drives. (05 Mar 2000) |
| acquired eccentric relation | An eccentric relation that is assumed by habit in order to bring the teeth into occlusion. (05 Mar 2000) |
| acquired epileptic aphasia | <syndrome> Acquired epileptic aphasia. The typical history is that of a child whose development is normal for several years and then, either suddenly or in a fluctuating manner, loses comprehension of speech and the ability to use speech to communicate. The seizures are of no specific type, and are mostly mild and infrequent partial or atypical absences. (12 Dec 1998) |
| acquired haemolytic anaemia | Nonhereditary acute or chronic anaemia associated with or caused by extracorpuscular factors, e.g., certain infectious agents, chemicals (including autoantibodies or therapeutic agents), burns, toxic materials from higher plant and animal forms (including snake venoms). (05 Mar 2000) |
| acquired haemolytic icterus | Icterus and anaemia occuring in association with a moderate degree of splenomegaly, increased fragility of red blood cells, and increased amounts of urobilin in the urine. Synonym: icteroanaemia. Origin: G. Ikteros (05 Mar 2000) |
| acquired hyperlipidaemia | <biochemistry> A condition of elevated blood triglycerides or blood cholesterol that is a result of secondary factors (for example poor diet, drug-related causes, diabetes, hypothyroidism, Cushing's syndrome). (27 Sep 1997) |
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