| ATCC | American Type Culture Collection |
|---|---|
| ATD | Alzheimer-type dementia; androstatrienedione; anthropomorphic test dummy; antithyroid drug; aqueous ... |
| beta [Greek letter beta] | an anomer of a carbohydrate; buffer capacity; carbon separated from a carboxyl by one other carbon i... |
| BHK | baby hamster kidney [cells]; type-B Hong Kong [influenza virus] |
| BlT | bleeding time; blood test; blood type, blood typing |
| type 2 diabetes | <endocrinology> Also referred to as adult-onset diabetes. More common in the middle-age, overweight individual. Usually treated by diet control, weight reduction or oral hypoglycemic agents. (27 Sep 1997) |
|---|---|
| type 2 glycogenosis | Glycogenosis due to lysosomal alpha-1,4-glucosidase deficiency, resulting in accumulation of excessive amounts of glycogen of normal chemical structure in heart, muscle, liver, and nervous system. Synonym: generalised glycogenosis, Pompe's disease. (05 Mar 2000) |
| type 3 dextrocardia | Displacement and rotation of the heart into the right side of the chest but without mirror transposition of the cardiac chambers. Synonym: dextroversion of the heart, false dextrocardia, type 3 dextrocardia. (05 Mar 2000) |
| type 3 glycogenosis | Glycogenosis due to amylo-1,6-glucosidase deficiency, resulting in accumulation of abnormal glycogen with short outer chains in liver and muscle. Synonym: Cori's disease, debranching deficiency limit dextrinosis, limit dextrinosis, Forbes' disease. (05 Mar 2000) |
| type 4 dextrocardia | Dextroposition of the heart by some disease of the lungs, pleura, or diaphragm. Synonym: type 4 dextrocardia. (05 Mar 2000) |
| type 4 glycogenosis | Familial cirrhosis of the liver with storage of abnormal glycogen; glycogenosis due to deficiency of 1,4-alpha-glucan branching enzyme, resulting in accumulation of abnormal glycogen with long inner and outer chains in liver, kidney, muscle, and other tissues. Synonym: Andersen's disease. (05 Mar 2000) |
| type 5 glycogenosis | Glycogenosis due to muscle glycogen phosphorylase deficiency, resulting in accumulation of glycogen of normal chemical structure in muscle. Synonym: McArdle's disease, McArdle's syndrome, McArdle-Schmid-Pearson disease, myophosphorylase deficiency glycogenosis. (05 Mar 2000) |
| type 6 glycogenosis | Glycogenosis due to hepatic glycogen phosphorylase deficiency, resulting in accumulation of glycogen of normal chemical structure in liver and leukocytes. Synonym: hepatophosphorylase deficiency glycogenosis, Hers' disease. (05 Mar 2000) |
| type 7 glycogenosis | Phosphofructokinase deficiency of muscle resulting in muscle cramps and myoglobinuria on extreme exertion. The clinical picture resembles type 5 glycogenosis. (05 Mar 2000) |
| type A behaviour | A behaviour pattern characterised by aggressiveness, ambitiousness, restlessness, and a strong sense of time urgency; associated with increased risk for coronary heart disease. (05 Mar 2000) |
| type a personality | Established behaviour pattern characterised by excessive drive and ambition, impatience, competitiveness, sense of time urgency, and poorly contained aggression. (12 Dec 1998) |
| type B behaviour | A behaviour pattern characterised by the absence or obverse of type A behaviour characteristics. (05 Mar 2000) |
| type culture | A type strain of microorganism preserved in a culture collection as the standard. (05 Mar 2000) |
| type genus | <zoology> The type of a taxon at the family group level - the nominal genus. (09 Jan 1998) |
| type horizon | <zoology> The geological stratum from which the name-bearing type of a nominal species or subspecies was collected. (09 Jan 1998) |