| BlT | bleeding time; blood test; blood type, blood typing |
|---|---|
| BT | base of tongue; bedtime; bitemporal; bitrochanteric; bladder tumor; Blalock-Taussig [shunt]; bleedin... |
| BTR | Bezold-type reflex; biceps tendon reflex |
| BZRP | benzodiazepine receptor peripheral [type] |
| CBBM | color blindness, blue mono-cone-monochromatic type |
| hyperlipoproteinaemia type III | A rather uncommon form of familial hyperlipaemia characterised by the presence of lipoproteins of abnormal composition. The main abnormal lipoproteins are called beta-vldl and have a different apoprotein content and a higher proportion of cholesterol relative to triglyceride than normal vldl. (12 Dec 1998) |
|---|---|
| hyperlipoproteinaemia type IV | A familial disorder characterised by an isolated elevation in the plasma level of endogenously synthesised triglyceride carried in vldl. It is considered to be an autosomal dominant trait. (12 Dec 1998) |
| hyperlipoproteinaemia type v | A severe familial adult-onset hypertriglyceridemia different from that due to lipoprotein lipase deficiency. (12 Dec 1998) |
| South African type porphyria | Porphyria characterised by abdominal pain and neuropsychiatric abnormalities, by dermal sensitivity to light and mechanical trauma, by increased faecal excretion of proto-and coproporphyrin, and by increased urinary excretion of d-aminolevulinic acid, porphobilinogen, and porphyrins; due to a deficiency of protoporphyrinogen oxidase; autosomal dominant inheritance. Synonym: protocoproporphyria hereditaria, South African type porphyria. (05 Mar 2000) |
| Naegeli type of monocytic leukaemia | A variant of granulocytic leukaemia with monocytosis in the peripheral blood. Synonym: Naegeli type of monocytic leukaemia. (05 Mar 2000) |
| name bearing type | <zoology> The type genus, type species, holotype, lectotype, series of syntypes, neotype, type slide, or hapantotype, that provides the objective standard of reference whereby the application of the name of a taxon can be determined. (09 Jan 1998) |
| neoplasms by histologic type | A collective term for the various histological types of neoplasms. It is more likely to be used by searchers than by indexers and catalogers. (12 Dec 1998) |
| stream-type fish | Fish that rear for a year or more in a stream. (09 Oct 1997) |
| Nezelof type of thymic alymphoplasia | Synonym: cellular immunodeficiency with abnormal immunoglobulin synthesis. (05 Mar 2000) |
| s-type cholinesterase | <enzyme> An enzyme that breaks down acetylcholine tostop its action. (22 May 1997) |
| S type lectin | <protein> One of two classes of lectin produced by animal cells. The classification of animal lectins into two classes, the other being the C type, was originally proposed by K.Drickamer. The carbohydrate binding activity of the S type lectins requires their cysteines to have free thiols and does not need divalent cations (c.f. C type lectins). They mostly have molecular masses in the range 14-16 kD and often form dimers and higher oligomers. The carbohydrate recognition domain contains a number of critically conserved amino acids and largely binds to _ galactosides. S type lectins certainly occur as cytoplasmic proteins but the existence of extracellular S type lectins is still a matter of debate. (18 Nov 1997) |
| nomenclatural type | The constituent element of a taxon to which the name of the taxon is permanently attached; the type of a species is preferably a strain (in special cases it may be a description, a preserved specimen or preparation, or an illustration); the type of a genus is a species; and the type of an order, family, or tribe is the genus on whose name the name of the higher taxon is based. (05 Mar 2000) |
| nutritional type cerebellar atrophy | A restricted type of cerebellar cortical degeneration, affecting particularly the Purkinje cells of the anterior and superior vermis; probably caused by thiamin deficiency; most frequently seen in chronic alcoholics and then called alcoholic cerebellar degeneration. (05 Mar 2000) |
| delayed type hypersensitivity | <immunology> Hypersensitivity (increased reaction by the body to a foreign substance such as an antigen or allergen) that does not appear until 24 to 48 hours after the body is exposed to the foreign substance. (09 Oct 1997) |
| Swiss type agammaglobulinaemia | Group of rare congenital disorders characterised by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. It is inherited as an x-linked or autosomal recessive defect. About half of the patients with autosomal recessive scid are deficient in the enzyme adenosine deaminase. (12 Dec 1998) |
| type |
A character used in printing. Generally of metal, each one is nearly or approximately an inch high, and rectangular in shape.
출처: www.collectionscanada.ca/presses/t15-300-e.html
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| type 1 diabetes |
Also called Juvenile Diabetes. Onset usually occurs in childhood or adolescence. The islet cells of the pancreas come under attack from the bodies T-Cells. This renders the body incapable of producing insulin. Sufferers must inject insulin to control sugar levels.
출처: www.abheritage.ca/abinvents/glossary.htm
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| type 2 diabetes |
Also called Adult Diabetes. The islets continue to produce insulin, but the body does not recognize them properly or the insulin produced is faulty. This form of the disease is often related to choices of diet and lifestyle and can be controlled by diet.
출처: www.abheritage.ca/abinvents/glossary.htm
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| type |
The data representation type used for data transfer and storage. Type implies certain transformations between the time of data storage and data transfer. The representation types defined in FTP are described in the Section on Establishing Data Connections.
출처: www.freesoft.org/CIE/RFC/959/4.htm
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| type 1 diabetes |
(dye-uh-BEET-eez) Previously known as
출처: win.niddk.nih.gov/publications/glossary/MthruZ.htm
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