| 영문 | abnormality, anomaly | 한글 | 이상, 비정상 |
|---|---|---|---|
| 설명 | 정상을 벗어난 성질 혹은 사실. anomaly, aberration 등도 이상 상태를 나타내는 것이지만 abnormality가 가장 넓은 의미의 이상이다. anomaly는 보통 선천적 이상을 의미하며, aberration은 맨 눈으로 보이지 않는 이상을 의미하는 경우가 많다. |
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| 영문 | duplication | 한글 | 중복 |
|---|---|---|---|
| 설명 | 1. 유전학에서 염색체의 일부가 여분으로 존재하고 있는 것으로, 이것이 정상의 염색체 보체에 인접하여 존재하는 수도 있고 떨어져 있는 경우도 있다. 2. 어떤 크기를 가진 DNA 부분이 염색체 상에서 중복하는 것으로, 염색체가 하나 혹은 수 개의 유전자로 되어 있는 두 개의 같은 군을 가진 염색체 이상. |
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| Dp | duplication; dyspnea |
|---|---|
| dup | duplication |
| HIVD | Herniation(Herniated) of Inter-Vertebral Disc - Cervical HIVD &... |
| JVP | [POMD P 49 - 52] 1) Jugular Vein Pressure 2) Jugular Venous Pulse ... |
| TOF | 1) Tetralogy Of Fallot ? CIx of Corrective Op ... |
| SAA | South Atlantic Anomaly |
|---|---|
| MCA | multiple congenital anomaly |
| gene duplication | <molecular biology> A class of DNA rearrangement that generates a supernumerary copy of a gene in the genome. This would allow each gene to evolve independently to produce distinct functions. Such a set of evolutionarily related genes can be called a gene family. (18 Nov 1997) |
|---|---|
| duplication | 1. The act of duplicating, or the state of being duplicated; a doubling; a folding over; a fold. 2. <biology> The act or process of dividing by natural growth or spontaneous action; as, the duplication of cartilage cells. <mathematics> Duplication of the cube, the operation of finding a cube having a volume which is double that of a given cube. Origin: L. Duplicatio: cf. F. Duplication. Source: Websters Dictionary (01 Mar 1998) |
| duplication cyst | A congenital cystic malformation attached to or originating from any part of the alimentary canal, from the base of the tongue to the anus, which reproduces the structure of the adjacent alimentary tract. (05 Mar 2000) |
| duplication of chromosomes | A chromosome aberration resulting from unequal crossing over or exchange of segments between two homologous chromosomes; one chromosome of the pair loses a small segment, while the other gains this segment; the chromosome gaining the segment has undergone duplication while its homologue has undergone deletion. See: haemoglobin Lepore. (05 Mar 2000) |
| Alder's anomaly | Coarse azurophilic granulation of leukocytes, especially granulocytes, which may be associated with gargoylism and Morquio's disease. (05 Mar 2000) |
| angle of anomaly | <ophthalmology> An obsolete term for the degree of deviation from parallelism of the visual axes of the eyes. (05 Mar 2000) |
| anomaly | A marked deviation from the normal standard, especially as a result of congenital defects. Origin: Gr. Anomalia (18 Nov 1997) |
| Aristotle's anomaly | When a small object is held between the first and second fingers crossed in such a way that it touches or presses upon skin surfaces which ordinarily are not pressed upon simultaneously by a single object, it is perceived falsely as two. (05 Mar 2000) |
| May-Hegglin anomaly | A disorder in which neutrophils and eosinophils contain basophilic structures known as Dohle or Amato bodies and in which there is faulty maturation of platelets, with thrombocytopenia; autosomal dominant inheritance. Synonym: May-Hegglin anomaly. (05 Mar 2000) |
| pelger-huet anomaly | An inherited defect interfering with normal nuclear lobulation of neutrophils and eosinophils. The nuclei appear rodlike, spherical, or dumbbell-shaped and their structure is coarse and lumpy. (12 Dec 1998) |
| Pelger-Huet nuclear anomaly | Congenital inhibition of lobulation in the nuclei of neutrophilic leukocytes; most cells present band or bilobulate appearance, and only an occasional cell is trilobed; it is not associated with disease, but may be confused with leukocyte "shift to left"; autosomal dominant inheritance. (05 Mar 2000) |
| Chediak-Steinbrinck-Higashi anomaly | <syndrome> An autosomal recessive disorder characterised by the presence of giant lysosomal vesicles in phagocytes and in consequence poor bactericidal function due to deficient secretion of myeloperoxidase by lysosomes. There is some perturbation of microtubule dynamics. There are abnormalities of granulation and nuclear structure of all types of leukocytes with malformation of peroxidase-positive granules, cytoplasmic inclusions, and Dohle bodies, often with hepatosplenomegaly, lymphadenopathy, anaemia, thrombocytopenia, roentgenologic changes of bones, lungs and heart, skin and psychomotor abnormalities, and susceptibility to infection. The condition usually results in death in childhood, before the age of 10. Reported from humans, albino Hereford cattle, mink, beige mice and killer whale. Compare: chronic granulomatous disease. Inheritance: autosomal recessive. Synonym: Beguez Cesar disease, Chediak-Higashi disease, Chediak-Steinbrinck-Higashi anomaly. (21 May 1997) |
| Rieger's anomaly | Mesodermal dysgenesis of cornea and iris, producing pupillary anomalies, posterior embryotoxon, and secondary glaucoma. Synonym: Rieger's anomaly. (05 Mar 2000) |
| Peters' anomaly | <syndrome> A congenital disorder originating from faulty separation of embryonic structures; it results in bilateral central corneal opacities, with an anterior ring attachment of the iridic pupillary border and anterior polar cataracts; associated with short-limbed dwarfism; autosomal dominant inheritance. See: iridocorneal endothelial syndrome. Synonym: Peters' anomaly. (05 Mar 2000) |
| morning glory anomaly | <ophthalmology, syndrome> A congenital anomaly of the optic disk in which there is a funnel-shaped hypoplastic optic nerve, which has a dot of white tissue at the centre, surrounded by an elevated anulus of chorioretinal pigment. The retinal vessels seen are multiple narrow bands at the edge of the disk. (22 Sep 2002) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|