Chromosome 17p13.1 deletion and 14q32 rearrangements in Bone marrow by FISH 81751-0
LOINC Code
| LOINC code | 81751-0 | ||
|---|---|---|---|
| name | Chromosome 17p13.1 deletion and 14q32 rearrangements in Bone marrow by FISH | ||
| description | This tests detects 17p13.1 (TP53 gene) deletions and 14q32 rearrangements by fluorescence in situ hybridization (FISH). Both genetic anomalies are associated with the development of multiple myeloma, a white blood cell cancer that affects plasma cells. | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | Chromosome region 17p13.1 deletion & chromosome region 14q32 rearrangements | ||
| 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 | Bone mar = Marrow (bone) | ||
| scale | Doc = Document: A document that could be in many formats (XML, narrative, etc.) | ||
| method | FISH | ||
Additional Names | |||
| short name | Chr 17p13.1 Del + 14q32 Rearr Mar FISH | ||
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.
| |||
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 | MIN - change to field other than name | ||
| change reason | Changed "17p13" to "17p13.1" in Component to clarify that the probe for this assay targets the p13.1 region of chromosome 17. | ||
Related Names | |||
| |||
| hierarchy paths | LOINC Home {component} LP432695-7 Laboratory LP29693-6 Molecular pathology LP7822-2 Chromosome LP32750-9 Deletions or Duplications LP190353-5 Chromosome 17p13.1 deletion and 14q32 rearrangements LP212129-3 Chromosome 17p13.1 deletion and 14q32 rearrangements | Bone marrow | Molecular pathology LP401807-5 LOINC Home {component} LP432695-7 Laboratory LP29693-6 Molecular pathology LP7822-2 Chromosome LP32750-9 Rearrangements LP7825-5 Chromosome 17p13.1 deletion and 14q32 rearrangements LP212129-3 Chromosome 17p13.1 deletion and 14q32 rearrangements | Bone marrow | Molecular pathology LP401807-5 | ||
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.
Thank you for choosing Find-A-Code, please Sign In to remove ads.
Quick, Current, Complete - www.findacode.com