Fetal chromosome 13+18+21+X+Y aneuploidy in Tissue by Molecular genetics method Nominal 57029-1
LOINC Code
| LOINC code | 57029-1 | ||
|---|---|---|---|
| name | Fetal chromosome 13+18+21+X+Y aneuploidy in Tissue by Molecular genetics method Nominal | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | Fetal chromosome 13+18+21+X+Y aneuploidy | ||
| property | Find = Finding | ||
| 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 | Tiss^Fetus Tiss = Tissue, unspecified | ||
| 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 | Molgen = Molecular Genetics: General class of methods used to detect genetic attributes on a molecular basis including RFL, PCR and other methods. | ||
Additional Names | |||
| short name | Chr 13+18+21+X+Y aneup Tiss Fetus | ||
Basic Attributes | |||
| class | MOLPATH | ||
| type | 1 Laboratory | ||
| order vs. observation | Both | ||
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. | |||
History/Usage | |||
| first released | |||
| last updated | 2.66 | ||
| last change type | NAM - change to Analyte/Component | ||
| change reason | Added "Fetal" to Component for consistency across terms that represent fetal aneuploidy and vary by System | ||
Related Names | |||
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