| genet | genetic, genetics |
|---|---|
| ADME | [drug] absorption, distribution, metabolism, and excretion |
| NIAMDD | National Institute of Arthritis, Metabolism, and Digestive Diseases |
| BM | Bachelor of Medicine; barium meal; basal medium; basal metabolism; basement membrane; basilar membra... |
| CMI | carbohydrate metabolism index; care management integration; case mix index; cell-mediated immunity; ... |
| inborn error of metabolism | A genetic biochemical disorder of a specific enzyme that forms a metabolic block, e.g., phenylketonuria. (05 Mar 2000) |
|---|---|
| inborn errors of metabolism | Term coined by A. Garrod in 1908 applying to heritable disorders of biochemistry. Examples include albinism, cystinuria (a cause of kidney stones) and phenylketonuria (pku) are a few of the hundreds of inborn errors of metabolism. (12 Dec 1998) |
| intermediary metabolism | Enzyme-catalysed processeswithin cells that extract energy from nutrientmolecules and use that energy to construct cellular components. (09 Oct 1997) |
| iron metabolism disorders | Disorders in the processing of iron in the body: its absorption, transport, storage, and utilization. (12 Dec 1998) |
| oxidative metabolism | Respiration in the biochemical sense. (18 Nov 1997) |
| electrolyte metabolism | The chemical changes that various essential minerals (e.g., sodium, potassium, calcium, magnesium) undergo in the tissues. (05 Mar 2000) |
| energy metabolism | Those metabolic reactions whose role is to release or to provide energy. (05 Mar 2000) |
| fat metabolism | Oxidation, decomposition, and synthesis of fats in the tissues. (05 Mar 2000) |
| fructose metabolism, inborn errors | Inherited abnormalities of fructose metabolism, which include three known autosomal recessive types: hepatic fructokinase deficiency (essential fructosuria), hereditary fructose intolerance, and hereditary fructose-1,6-diphosphatase deficiency. Essential fructosuria is a benign asymptomatic metabolic disorder caused by deficiency in fructokinase, leading to decreased conversion of fructose to fructose-1-phosphate and alimentary hyperfructosaemia, but with no clinical dysfunction; may produce a false-positive diabetes test. (12 Dec 1998) |
| behavioural genetics | The study of heritable factors in behavioural patterns, as by pedigree analysis, biochemical abnormality, or karyotypic analysis. (05 Mar 2000) |
| biochemical genetics | The study of genetics in terms of the chemical (biochemical) events involved, as in the manner in which DNA molecules replicate and control the synthesis of specific enzymes by the genetic code. (05 Mar 2000) |
| biometrical genetics | <study> The mathematical approach to the study of the inheritance of different phenotypes, or physical characteristics, as a result of plant or animal breeding. (09 Oct 1997) |
| Galtonian-Fisher genetics | The genetics of measurable traits determined by multiple loci which make contributions that are independent, additive, and approximately equal. Synonym: multilocal genetics. (05 Mar 2000) |
| galtonian genetics | The study of traits by analysis of the first two moments of metrical data; the preferred method for analysis of traits following the multivariate gaussian distribution. (05 Mar 2000) |
| palindrome in genetics | A palindrome is a word that reads the same in both directions as, for example, the names eve or anna. In genetics, a palindrome is a DNA or RNA sequence that reads the same in both directions. The sites of many restriction enzymes that cut (restrict) DNA are palindromes. Palindromic rheumatism is a form of joint inflammation whereby the joints involved appears to change periodically from one region of the body to another and back again. (12 Dec 1998) |