| misc | miscarriage; miscellaneous |
|---|---|
| TAT | tetanus antitoxin; thematic apperception test; thematic aptitude test; thrombin-antithrombin complex... |
| DASD | Direct Access Storage Device = RAM |
| SPD | Storage Pool Disease |
| CESD | cholesterol ester storage disease |
| TAT | Tray Agglutination Test |
|---|---|
| CESD | Cholesterol ester storage disease |
| GSD | Glycogen Storage Disease |
| GSDII | Glycogen Storage Disease type II |
| GSD 1a | Glycogen storage disease type 1a |
shelf force
channel-shoulder-pin attachment
| tray | Origin: OE. Treye, AS. Treg. Cf. Trough. 1. A small trough or wooden vessel, sometimes scooped out of a block of wood, for various domestic uses, as in making bread, chopping meat, etc. 2. A flat, broad vessel on which dishes, glasses, etc, are carried; a waiter; a salver. 3. A shallow box, generally without a top, often used within a chest, trunk, box, etc, as a removable receptacle for small or light articles. Source: Websters Dictionary (01 Mar 1998) |
|---|---|
| Blumer's shelf | A shelf palpable by rectal examination, due to metastatic tumour cells gravitating from an abdominal cancer and growing in the rectovesical or rectouterine pouch. Synonym: Blumer's shelf. (05 Mar 2000) |
| palatal shelf | A medially directed outgrowth of the embryonic maxilla; when fused with its opposite number it forms the secondary palate. (05 Mar 2000) |
| rectal shelf | A shelf palpable by rectal examination, due to metastatic tumour cells gravitating from an abdominal cancer and growing in the rectovesical or rectouterine pouch. Synonym: Blumer's shelf. (05 Mar 2000) |
| vocal shelf | One of Ferrein's cords; the sharp edge of a fold of mucous membrane overlying the vocal ligament and stretching along either wall of the larynx from the angle between the laminae of the thyroid cartilage to the vocal process of the arytenoid cartilage; the vocal folds are the agents concerned in voice production. Synonym: plica vocalis, chorda vocalis, labium vocale, true vocal cord, vocal cord, vocal shelf. (05 Mar 2000) |
| shelf | Origin: OE. Shelfe, schelfe, AS. Scylfe; akin to G. Schelfe, Icel. Skjalf. In senses 2 & 3, perhaps a different word (cf. Shelve,). 1. A flat tablet or ledge of any material set horizontally at a distance from the floor, to hold objects of use or ornament. 2. A sand bank in the sea, or a rock, or ledge of rocks, rendering the water shallow, and dangerous to ships. "On the tawny sands and shelves." (Milton) "On the secret shelves with fury cast." (Dryden) 3. <chemical> A stratum lying in a very even manner; a flat, projecting layer of rock. 4. A piece of timber running the whole length of a vessel inside the timberheads. To lay on the shelf, to lay aside as unnecessary or useless; to dismiss; to discard. Source: Websters Dictionary (01 Mar 1998) |
| shelf procedure | Insertion of a graft from the ilium into the roof of the acetabulum for congenital dislocation of the hip. (05 Mar 2000) |
| dental shelf | dental ledge |
| brancher glycogen storage disease | Type of glycogen storage disease, due to deficiency of amylo-1,4-1,6-transglucosidase (brancher enzyme). Synonym: brancher deficiency glycogenosis, debrancher deficiency. (05 Mar 2000) |
| glycogen storage disease | <hepatology> A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalised storage of glycogen occurs, sometimes with prominent cardiac involvement. Synonym: glycogenosis (12 Sep 2002) |
| glycogen storage disease type I | <disease> An autosomal recessive disease in which gene expression of glucose-6-phosphatase is absent, resulting in hypoglycaemia due to lack of glucose production. Accumulation of glycogen in liver and kidney leads to organomegaly, particularly massive hepatomegaly. Increased concentrations of lactic acid and hyperlipidemia appear in the plasma. Clinical gout often appears in early childhood. Inheritance: autosomal recessive. (12 Dec 1998) |
| glycogen storage disease type II | <disease> Glycogenosis due to alpha-1,4-glucosidase (acid maltase) deficiency. It affects muscle, heart, and other organs. (12 Dec 1998) |
| glycogen storage disease type III | <disease> An autosomal recessive metabolic disorder due to deficient expression of amylo-1,6-glucosidase (one part of the glycogen debranching enzyme system). The clinical course of the disease is similar to that of glycogen storage disease type I, but milder. Massive hepatomegaly, which is present in young children, diminishes and occasionally disappears with age. Levels of glycogen with short outer branches are elevated in muscle, liver, and erythrocytes. Six subgroups have been identified, with subgroups type IIIa and type IIIb being the most prevalent. Inheritance: autosomal recessive (12 Dec 1998) |
| glycogen storage disease type IV | <disease> An autosomal recessive metabolic disorder due to a deficiency in expression of branching enzyme (alpha-1,4-glucan-6-alpha-glucosyltransferase), resulting in an accumulation of abnormal glycogen with long outer branches. Clinical features are muscle hypotonia and cirrhosis. Death from liver disease usually occurs before age 2. Inheritance: autosomal recessive (12 Dec 1998) |
| glycogen storage disease type V | <disease> Glycogenosis due to muscle phosphorylase deficiency. Characterised by painful cramps following sustained exercise. Inheritance: autosomal recessive (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|