| 영문 | screening | 한글 | 검색, 선별 |
|---|---|---|---|
| 설명 | 1. 보기에는 건강한 것과 같이 보이면서 질병에 걸려있다고 생각되는 사람들을 골라내기 위한 검사. 질병의 진단을 의도한 것은 아니고 다수의 수전자 중에서 비교적 간단한 방법으로 의심이 가는 자를 골라내는 것을 목적으로 한다. 선출된 자는 더욱 상세한 검사를 받을 필요가 있다. 2. 시험이나 검사와 같은 예비적 절차, 조사가 더 필요한 장애의 가장 특징적인 징후를 찾아내기 위해 시행한다. 3. 집단선별검사, 고혈압과 같은 특정병이나 장애를 찾아내기 위해 큰 표본을 이용하는 검사. |
||
| CHARGE Associations | Coloboma Heart disease Atresia choanae Reta... |
|---|---|
| CHARGE | coloboma, heart disease, atresia choanae, retarded growth and retarded development and/or CNS anomal... |
| short-FRAME | short stature-facial anomalies-Rieger anomaly-midline anomalies-enamel defects [syndrome] |
| DAST | drug abuse screening test; drug and alcohol screening test |
| AN | acanthosis nigricans; acne neonatorum; acoustic neuroma; adult, normal; ala nasi; amyl nitrate; aneu... |
| ANC | Antenatal Care |
|---|---|
| ANC | Antenatal clinics |
| DVAs | Developmental venous anomalies |
| MPAs | Minor physical anomalies |
| MCA | Multiple congenital anomalies |
| antenatal | <epidemiology> The period between conception and birth. Same as prenatal. (05 Dec 1998) |
|---|---|
| antenatal diagnosis | Determination of the nature of a pathological condition or disease in the postimplantation embryo, foetus, or pregnant female before birth. (12 Dec 1998) |
| coronary artery anomalies | <radiology> Associated with, tetralogy of Fallot (TOF), transposition of great vessels (TGV) (12 Dec 1998) |
| coronary vessel anomalies | Defects of coronary arteries or veins including anomalous origin, arteriovenous fistula or aneurysm, myocardial bridging, or other abnormalities of structure or development. (12 Dec 1998) |
| genome, chromosomal | All of the genetic information in the chromosomes of an organism. For humans, that is all of the DNA contained in our normal complement of 46 rod-like chromosomes in virtually every cell in the body. (Mature red blood cells, for one exception, have no nucleus and therefore no chromosomes). The chromosomal genome is synonymous with the nuclear genome. Together with the mitochondrial genome, it constitutes the genome of the human being. (12 Dec 1998) |
| chromosomal | Pertaining to chromosomes. (18 Nov 1997) |
| chromosomal aberration | Any abnormality of a chromosome's number or structure. (09 Oct 1997) |
| chromosomal deletion | A microscopically evident loss of part of a chromosome. See: monosomy. (05 Mar 2000) |
| chromosomal gap | A localised area of thinning in a chromatid which may simulate a complete break. (05 Mar 2000) |
| chromosomal instability syndromes | A group of mendelian conditions associated with chromosomal instability and breakage in vitro, they often manifest an increased tendency to certain types of malignancies. See: Bloom's syndrome, fragile X syndrome, xeroderma pigmentosum. (05 Mar 2000) |
| chromosomal map | A formal, stylised representation of the karyotype and of the positioning and ordering on it of those loci that have been localised by any of several mapping methods. (05 Mar 2000) |
| chromosomal mutation | Can refer to any of a number of DNA mutations which results in a change in the protein encoded by the mutated gene, such as point mutations, insertion or deletion mutations (frameshift mutations), or nonsense mutations. More often this refers to mutations involving chromosomes, such as the inversion of part of one chromosome such that the inverted part no longer matches with its homologous pair, a translocation of one part of a chromosome to a different chromosome, deletions of parts of chromosomes, or accidents which happen during the division of the nucleus like the unequal portioning of chromosomes between the daughter cells. (09 Oct 1997) |
| chromosomal proteins, non-histone | Nucleoproteins which in contrast to histones are acid insoluble. They are involved in chromosomal functions; e.g. They bind selectively to DNA, stimulate transcription resulting in tissue-specific RNA synthesis and undergo specific changes in response to various hormones or phytomitogens. (12 Dec 1998) |
| chromosomal region | That part of a chromosome defined either by anatomical details, notably banding, or by its linkages (linkage group). (05 Mar 2000) |
| chromosomal RNA | RNA associated with the chromosome (not mRNA, tRNA, or rRNA) that may have a role in transcription. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|