| OMIM | Online Mendelian Inheritance in Man [database] |
|---|---|
| MEN | Multiple Endocrine Neoplasia ; AD Trait 1. MEN Type I(= Wermer Syndro... |
| PBT | Paul-Bunnell test; phenacetin breath test; piebald trait; profile-based therapy |
| PTD | percutaneous transluminal dilatation; permanent total disability; personality trait disorder; preter... |
| SCT | secretin; sex chromatin test; sexual compatibility test; sickle-cell trait; sperm cytotoxicity; spin... |
| OMIM | On-Line Mendelian Inheritance in Man |
|---|---|
| QTL | Aquantitative trait locus |
| QTL | Quantitative Trait Loci |
| QTLs | Quantitative Trait Loci |
| SCT | Sickle cell trait |
| mendelian trait | A categorical trait that segregates in accordance with a single-locus genetic system. (05 Mar 2000) |
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| mendelian | Referring to the Austrian monk Gregor Mendel (1822-84) who formulated laws forming the foundation of classical genetics. (12 Dec 1998) |
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| mendelian character | An inherited character under the control of a single locus (although perhaps modified by genes at other loci). (05 Mar 2000) |
| mendelian genetics | The study of the pattern of segregation of phenotypes under the control of genetic loci taken one at a time. (05 Mar 2000) |
| Mendelian inheritance | <genetics> Inheritance of characters according to the classical laws formulated by Gregor Mendel, which give the classic ratios of segregation in the F2 generation. In sexually reproducing organisms, any process of heredity explicable in terms of chromosomal segregation, independent assortment and homologous exchange. (18 Nov 1997) |
| Mendelian Inheritance in Man | A standard, comprehensive, perpetually updated reference source for traits in humans that have been shown to be mendelian or that are thought on reasonable grounds to be so. Each entry has a six-digit catalog number. Those securely established (by molecular biology or by extensive clinical studies) are marked with an asterisk. (05 Mar 2000) |
| mendelian ratio | The ratio of progeny with a particular phenotypes or genotypes expected in accordance with Mendel's law among the offspring of matings specified as to genotype or phenotype. (05 Mar 2000) |
| Bombay trait | A rare recessive trait at a locus that ordinarily manufactures H substance, the precursor from which the A and B phenotypes are elaborated; the mutant causes failure to produce H substance and no matter what the genotype at the ABO locus, the phenotype is O. The Bombay phenomenon is epistatic to the ABO locus. Origin: Bombay, India, where first reported (05 Mar 2000) |
| galtonian trait | A quantitative genetic trait due to contributions from many more of less equally important loci that resembles a continuous trait. (05 Mar 2000) |
| recessive trait | See: dominance of traits. (05 Mar 2000) |
| marker trait | A trait that may be of little importance in itself but which by association, linkage, or other means facilitates the detection, anticipation, or understanding of a disease or (for genetic diseases) the localization of the causative gene on the karyotype. (05 Mar 2000) |
| categorical trait | <genetics> A feature that can conveniently and effectively be analyzed by sorting into classes either because there is no satisfactory way of measuring it (as with blood groups) or because it falls into natural classes so that the variation among classes far exceeds that within classes (e.g., the phenotypic effects of many enzyme polymorphisms); existence of categories suggests but does not prove the operation of a major, simple, underlying cause. Synonym: qualitative trait. (05 Mar 2000) |
| penetrant trait | A trait that in the appropriate genotypes is phenotypically manifest; strictly, it is the trait that is penetrant, not the gene. See: penetrance. (05 Mar 2000) |
| chromosomal trait | A trait dependent on a recurrent chromosomal aberration. (05 Mar 2000) |
| codominant trait | See: codominant. (05 Mar 2000) |
| sickle cell trait | <haematology> This condition occurs in people who have one of two possible genes (i.e., they are heterozygous forthe allele) that code for the defective haemoglobin responsible for sickle cell anaemia. The coditionis diagnosed by exposing an individual's red blood cells to a low oxygen environment, if the trait is present, the cells will turn to a sickle shape. People with this trait may suffer milder symptoms of sickle cell anaemia, or may have no symptoms. Some scientists believe the trait actually provides an evolutionary advantage in tropical environments because the slightly altered shape of the blood cells causes a person to be more resistant to malaria. (09 Oct 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|