Genetic risk algorithm 74021-7
LOINC Code
| LOINC code | 74021-7 | ||
|---|---|---|---|
| name | Genetic risk algorithm | ||
| description | The genetic algorithm (e.g. BRCAPRO), or computer program, used to predict whether a patient has an inherited mutation in a given gene (e.g. BRCA1) and/or to determine their risk for developing a disease. The genetic algorithms are based on personal and family medical histories of a disease, such as breast and ovarian cancer. This term is based on, but not limited in use to, the Genetic Algorithm Used variable in the Family History section of the V2 VMR, based on the Family History Standard Implementation Guide (US Realm) 2012. | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | Genetic risk algorithm | ||
| property | Type = Type: The Property Type is used for assays that identify the specific analyte in cases when the baseline presence of the analyte is known. | ||
| time | Pt = Point in time: To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements. | ||
| system | ^Patient | ||
| scale | Nom = Nominal: Nominal or categorical responses that do not have a natural ordering. (e.g., names of bacteria, reported as answers, categories of appearance that do not have a natural ordering, such as, yellow, clear, bloody. | ||
| method | |||
Additional Names | |||
| short name | Genetic algorithm | ||
Basic Attributes | |||
| class | H&P.HX | ||
| type | 2 Clinical | ||
| order vs. observation | Observation | ||
Associated Observations | |||
LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations. | |||
Member of these Panels | |||
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History/Usage | |||
| first released | |||
| last updated | 2.46 | ||
| last change type | MIN - change to field other than name | ||
Related Names | |||
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