| DASD | Direct Access Storage Device = RAM |
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| SPD | Storage Pool Disease |
| CESD | cholesterol ester storage disease |
| CSC | blow on blow (administration of small amounts of drugs at short intervals) [Fr. coup sur coup]; coll... |
| DASD | direct access storage device |
| CESD | Cholesterol ester storage disease |
|---|---|
| GSD | Glycogen Storage Disease |
| GSDII | Glycogen Storage Disease type II |
| GSD 1a | Glycogen storage disease type 1a |
| GSD I | Glycogen storage diseases type I |
| storage | 1. The act of depositing in a store or warehouse for safe keeping; also, the safe keeping of goods in a warehouse. 2. Space for the safe keeping of goods. 3. The price changed for keeping goods in a store. Storage battery. <physics> See the Note under Battery. Source: Websters Dictionary (01 Mar 1998) |
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| storage disease | <disease> Another name for lysosomal diseases. (18 Nov 1997) |
| storage granule | 1. <cell biology> Membrane bounded vesicles containing condensed secretory materials (often in an inactive, zymogen, form). Otherwise known as zymogen granules or condensing vacuoles. 2. Granules found in plastids or in cytoplasm, assumed to be food reserves, often of glycogen or other carbohydrate polymer. (18 Nov 1997) |
| storage pool disease | <disease> A form of congenital platelet functional defect that result in prolongation of the bleeding time. (27 Sep 1997) |
| storage protein deamidase | <enzyme> Deamidates glutaminyl residues; isolated from germinating wheat grains Registry number: EC 3.5.1.- Synonym: seed storage protein deamidase (26 Jun 1999) |
| 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) |
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| 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) |
| glycogen storage disease type VI | <disease> A hepatic glycogen storage disease in which there is an apparent deficiency of hepatic phosphorylase activity. However, studies have not been able to distinguish between phosphorylase deficiency and phosphorylase kinase deficiency in patients with hepatic glycogenosis. (12 Dec 1998) |
| glycogen storage disease type VII | <disease> An autosomal recessive muscle glycogen storage disease in which there is deficient expression of muscle phosphofructokinase activity, resulting in increased concentrations of glucose-6-phosphate and fructose-6-phosphate and low concentrations of fructose-1,6-diphosphate in muscle tissue. Glycogen storage in muscle is increased, perhaps due to activation of glycogen synthase by accumulated glucose-6-phosphate. It has been proposed that shunting of glucose-6-phosphate and fructose-6-phosphate into the pentose phosphate pathway may result in increased synthesis of purines and pyrimidines, causing hyperuricaemia and gout. Erythrocytes from patients may show decreased phosphofructokinase activity and 2,3-diphosphoglycerate deficiency. Exercise intolerance is present and severe congenital muscular dystrophy has been reported. Inheritance: autosomal recessive (12 Dec 1998) |
| glycogen storage disease type VIII | <disease> An x-linked recessive hepatic glycogen storage disease resulting from lack of expression of phosphorylase-b-kinase activity. Symptoms are relatively mild; hepatomegaly, increased liver glycogen, and decreased leukocyte phosphorylase are present. Liver shrinkage occurs in response to glucagon. Inheritance: X-linked recessive (12 Dec 1998) |
| cholesterol ester storage disease | A rare benign adult form of inherited lysosomal lipid storage disease that is due to deficiency of acid lipase. It results in an accumulation of neutral lipids, particularly cholesterol esters, within cells (particularly leukocytes, fibroblasts, and liver cells). It is an allelic variant of wolman disease. (12 Dec 1998) |
| phytanic acid storage disease | A genetic disorder of the fatty acid phytanic acid which accumulates and causes a number of progressive problems including polyneuritis (inflammation of numerous nerves), diminishing vision (due to retinitis pigmentosa), and wobbliness (ataxia) caused by damage to the cerebellar portion of the brain (cerebellar ataxia). (12 Dec 1998) |
| computer storage devices | Devices capable of receiving data, retaining data for an indefinite or finite period of time, and supplying data upon demand. (12 Dec 1998) |
| platelet storage pool deficiency | A group of disorders characterised by a decrease or lack of platelet dense bodies in which the releasable pool of adenine nucleotides and 5ht are normally stored. (12 Dec 1998) |
| cystine storage disease | Lysosomal storage disorders of unknown molecular defect, characterised by widespread deposition of cystine crystals in reticuloendothelial cells. (12 Dec 1998) |
| storage |
the act of storing something storehouse: a depository for goods; "storehouses were built close to the docks" the commercial enterprise of storing goods and materials (computer science) the process of storing information in a computer memory or on a magnetic tape or disk memory: an electronic memory device; "a memory and the CPU form the central part of a computer to which peripherals are attached" repositing: depositing in a warehouse; "they decided to reposition their furniture in a recommended repository in Brooklyn"; "my car is in storage"; "publishers reduced print runs to cut down the cost of warehousing"
출처: wordnet.princeton.edu/perl/webwn
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| storage |
Facilities engaged in the treatment, storage, or disposal of hazardous waste.
출처: www.epa.gov/epaoswer/hazwaste/ldr/glossary.htm
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| storage |
The volume of water in a reservoir at a given time.
출처: www.streamnet.org/pub-ed/ff/Glossary/glossarydam.h...
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| storage |
Holding of program instructions and data for use by the computer. Temporary storage while the computer is running is provided by the RAM, and permanent storage is available on disk and tape.
출처: www.micro2000uk.co.uk/hardware_glossary.htm
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| storage |
Bulk butter should be kept in poly-lined cartons under refrigerated (32 to 38
출처: webexhibits.org/butter/glossary-sz.html
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| storage | depositing in a warehouse |
|---|---|
| storage | the act of storing something |
| storage | the commercial enterprise of storing goods and materials |
| storage | an electronic memory device |
| storage | a depository for goods |
| storage | (computer science) the process of storing information in a computer memory or on a magnetic tape or disk |
| storage | the space in a ship or aircraft for storing cargo |
| storage | a voltaic battery that stores electric charge |
| storage | a cell that can be recharged |
| storage | a device that preserves information for retrieval |
| storage | a storage compartment for clothes and valuables |
| storage | container consisting of a set of magnets set in a doughnut-shaped ring around which charged particles from an accelerator can be kept circulating until they are used |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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