Informative
Term · Oncology and biomedicine · MLC-T-ONC-004313
In genetic testing, a test result that reveals definitively the presence or absence of the germline genetic alteration associated with the hereditary disorder being assessed. In linkage analysis, the ability to distinguish between maternally inherited and paternally inherited DNA markers (polymorphisms) within or near a given gene of interest.
| Identifier | MLC-T-ONC-004313 |
|---|---|
| Field | Oncology and biomedicine |
| References | NCI Dictionary of Genetics Terms |
Record as JSON
{
"id": "MLC-T-ONC-004313",
"term": "Informative",
"field": "Oncology and biomedicine",
"definition": "In genetic testing, a test result that reveals definitively the presence or absence of the germline genetic alteration associated with the hereditary disorder being assessed. In linkage analysis, the ability to distinguish between maternally inherited and paternally inherited DNA markers (polymorphisms) within or near a given gene of interest.",
"references": [
"NCI Dictionary of Genetics Terms"
],
"url": "https://mlchart.com/terminology/oncology/informative/"
}
Record 9,254 of 17,717 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.