LOINCActiveBoth

LOINC Code 81850-0: 11p15 methylation and del+dup Molgen Doc (Amn fld)

81850-0 is a LOINC code used to identify 11p15 methylation and del+dup Molgen Doc (Amn fld) in laboratory and clinical observation data. You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges. LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component Chromosome region 11p15 methylation & deletion+duplication. It is commonly used with the system or sample type Amnio fld.

Reviewed by HealthAssure Clinical TeamUpdated 21 May 2026

What is this code?

LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component Chromosome region 11p15 methylation & deletion+duplication. It is commonly used with the system or sample type Amnio fld.

When is it used?

  • Used in lab systems, EHRs, and clinical data exchange.
  • May identify a test, observation, survey item, or clinical document request rather than a diagnosis.
  • Status: ACTIVE
  • Order vs observation: Both
  • Method: Molgen

What it does not mean

  • The code identifies the observation or test, not the actual result.

Key facts

  • Chromosome region 11p15 methylation and deletion+duplication in Amniotic fluid by Molecular genetics method
  • Chromosome region 11p15 methylation & deletion+duplication
  • 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).
  • AF; Amn; Amn fl; Amnio; Amniotic flu; Amniotic fluid; Amplification; Beckwith Wiedemann Syndrome; BWS; Chr 11p15; Chr 11p15 methylation + deletion+duplication; Chromosom; Chromosomes; Cyto loc; Del; Del+Dup; Deletions; Document; Dp; Finding; Findings; Genetics; Gyn; Gynecology; Heredity; Heritable; Inherited; Methyl + Del+Dup; Molecular genetics; Molecular pathology; MOLPATH; OB; ObGyn; Obstetrics; PCR; Point in time; Random; RSS; Russell-Silver Syndrome

Where you may see this code

You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges.

Common synonyms

11p15 methylation and del+dup Molgen Doc (Amn fld)Chromosome region 11p15 methylation and deletion+duplication in Amniotic fluid by Molecular genetics methodChr 11p15 Methyl + Del+Dup AmnChromosome region 11p15 methylation & deletion+duplicationMOLPATH11p15 methylation and deletion/duplication analysis, Amniotic fluidFind

Frequently asked questions

Code details

Code81850-0
SystemLOINC
Display name11p15 methylation and del+dup Molgen Doc (Amn fld)
DescriptionChromosome region 11p15 methylation & deletion+duplication
Short nameChr 11p15 Methyl + Del+Dup Amn
ComponentChromosome region 11p15 methylation & deletion+duplication
PropertyFind
TimingPt
System (specimen)Amnio fld
ScaleDoc
MethodMolgen
ClassMOLPATH
StatusACTIVE
Order/ObservationBoth

Flags

BillableNo
Valid clinical useNo

Source

SourceLOINC
Version2.82
Releasemain
First released2.56
Last changed2.65

Consumer names

11p15 methylation and deletion/duplication analysis, Amniotic fluid

Part names

Chromosome region 11p15 methylation & deletion+duplicationFindPtAmnio fldDocMolgenFindingPoint in time (spot)Amniotic fluidMolecular genetics

About this content

This page is prepared by HealthAssure's clinical team using official coding standards from LOINC. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.

LOINC Code 81850-0 | HealthAssure