| ECG | Electro-Cardio-Graphy(-Gram); 심전도 = EKG 1. Conducting System Structu... |
|---|---|
| JVP | [POMD P 49 - 52] 1) Jugular Vein Pressure 2) Jugular Venous Pulse ... |
| rea | rearrangement |
| NAD | neutrophil actin dysfunction; new antigenic determinant; nicotinamide adenine dinucleotide; nicotini... |
| BES | balanced electrolyte solution; Baltimore Eye Study |
| CCR | complex chromosomal rearrangement |
|---|---|
| i | Individual |
| IPA | Individual Practice Association |
| IAT | individual anaerobic threshold |
| AIMS | Abnormal Involuntary Movement Scale |
| individual | Marked by a distinctness and a complexity within a unity that characterises organised things, concepts, organic beings and persons. (18 Nov 1997) |
|---|---|
| individual differences | In clinical psychology, deviations of individuals from the group average or from each other. (05 Mar 2000) |
| individual psychology | A theory of human behaviour emphasizing humans' social nature, strivings for mastery, and drive to overcome, by compensation, feelings of inferiority. Synonym: adlerian psychoanalysis, adlerian psychology. (05 Mar 2000) |
| individual therapy | A psychotherapeutic session involving only two persons, the therapist and the patient. Compare: group psychotherapy. Synonym: individual therapy. (05 Mar 2000) |
| individual tolerance | Tolerance to a drug that the person has never received before. (05 Mar 2000) |
| autosomal | Pertaining to an autosome. (05 Mar 2000) |
| autosomal dominant | <genetics> Requires only one affected parent have the trait to pass it to offspring. (02 Jan 1998) |
| autosomal gene | A gene located on any chromosome other than the sex chromosomes (X or Y). (05 Mar 2000) |
| autosomal recessive | <genetics> Mutation carried on an autosome that is deleterious only in homozygotes. (02 Jan 1998) |
| recessive, autosomal | A gene on a nonsex chromosome (an autosome) that expresses itself only when there is no different gene present at that locus (spot on the chromosome). For example, cystic fibrosis (cf) is an autosomal recessive disorder. A cf child has the cf gene on both chromosome 7's (and so is said to be homozygous for cf). (12 Dec 1998) |
| kidney, polycystic, autosomal dominant | A genetic disorder with autosomal dominant inheritance characterised by multiple cysts in both kidneys and progressive deterioration of renal function. It is usually caused by a mutant gene at the pkd1 locus on the short arm of chromosome 16, though mutations elsewhere in the genome can also cause the disease. The age of onset of symptoms varies widely. (12 Dec 1998) |
| kidney, polycystic, autosomal recessive | Rare genetic disorder with autosomal recessive inheritance characterised by multiple cysts in both kidneys and associated hepatic lesions. Serious manifestations are usually present at birth and there is high perinatal mortality. (12 Dec 1998) |
| abnormal | Not normal, contrary to the usual structure, position, behaviour or rule. (06 Oct 1997) |
| abnormal cleavage of cardiac valve | Congenital malformation of a valve leaflet with a defect extending from the free margin. (05 Mar 2000) |
| abnormal correspondence | Abnormal correspondence, a condition, frequent in strabismus, in which corresponding retinal points do not have the same visual direction; the fovea of one eye corresponds to an extrafoveal area of the fellow eye. Synonym: abnormal correspondence. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|