PRF1 gene targeted mutation analysis in Amniotic fluid by Molecular genetics method 34493-7
LOINC Code
| LOINC code | 34493-7 | ||
|---|---|---|---|
| name | PRF1 gene targeted mutation analysis in Amniotic fluid by Molecular genetics method | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | PRF1 gene targeted mutation analysis | ||
| 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 | Amnio fld = Amniotic fluid | ||
| scale | Doc = Document: A document that could be in many formats (XML, narrative, etc.) | ||
| 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 | PRF1 gene Mut Anl Amn | ||
Basic Attributes | |||
| class | MOLPATH.MUT | ||
| 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. | |||
Member of these Panels | |||
History/Usage | |||
| first released | |||
| last updated | 2.66 | ||
| last change type | MAJ - change to name field other than Component; | ||
| change reason | Based on LOINC Committee review (June 2016), "targeted" was added to the Component to clarify that this test is looking for a specific set of mutations as described in the LOINC User Guide under the Molecular Genetics section.; Based on LOINC Committee review (June 2019), updated the Property from "Prid" to "Find" and Scale from "Nar" to "Doc" to align with the current LOINC model for naming collections of information reported in narrative and/or structured formats. | ||
Related Names | |||
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