Cancer related multigene analysis in Blood or Tissue by Molecular genetics method 73977-1
LOINC Code
| LOINC code | 73977-1 | ||
|---|---|---|---|
| name | Cancer related multigene analysis in Blood or Tissue by Molecular genetics method | ||
| description | Multigene analysis for cancer-related variants is performed by various molecular techniques, including multiplex PCR and next generation sequencing (NGS), to identify genetic variants that may increase a person's risk for various types of cancer and help determine treatment options. Testing may be performed on genomic DNA from whole blood, bone marrow, and tumor specimens. | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | Cancer related multigene 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 | Bld/Tiss Bld = Whole blood Tiss = Tissue, unspecified | ||
| 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 | Cancer multigene analysis Bld/T | ||
Basic Attributes | |||
| class | MOLPATH | ||
| type | 1 Laboratory | ||
| order vs. observation | Both | ||
Ask At Order Entry | |||
Ask at Order Entry (AOE) observations for a clinical observation or laboratory test. A LOINC term may represent a single AOE observation or a panel containing several AOE observations.
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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 | |||
| test rank | 7461 of 2000 most commonly performed tests by labs in USA | ||
| first released | |||
| last updated | 2.73 | ||
| last change type | MIN - change to field other than name | ||
| change reason | Release 2.72: COMPONENT: Updated to align with current naming model in LOINC for multigene studies.; Previous Releases: 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.; Updated Property and Scale from Prid/Nar to Find/Doc based on the current model in LOINC for genetic test results containing a collection of data and reported in either structured or unstructured (narrative) formats. | ||
Related Names | |||
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Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2024, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.
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