Chromosome region 11p15 methylation and deletion+duplication in Amniotic fluid by Molecular genetics method 81850-0
LOINC Code
LOINC code | 81850-0 | ||
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name | Chromosome region 11p15 methylation and deletion+duplication in Amniotic fluid by Molecular genetics method | ||
description | The methylation status and copy numbers of the 11p15 chromosome region can be determined by various methods, including methylation-specific PCR and multiplex ligation-dependent probe amplification (MS-MLPA). This test is performed to detect causes of Beckwith-Wiedemann Syndrome (BWS) and Russell-Silver Syndrome (RSS). | ||
status | ACTIVE | ||
Fully-Specified Name | |||
component | Chromosome region 11p15 methylation & deletion+duplication | ||
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 | Chr 11p15 Methyl + Del+Dup Amn | ||
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 | |||
first released | |||
last updated | 2.65 | ||
last change type | MIN - change to field other than name | ||
Related Names | |||
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