LOINCActiveBoth

LOINC Code 103844-7: HBA1 and HBA2 gene del Molgen Doc (Amnio fld/CVS)

103844-7 is a LOINC code used to identify HBA1 and HBA2 gene del Molgen Doc (Amnio fld/CVS) 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 HBA1 & HBA2 gene deletion. It is commonly used with the system or sample type Amnio fld/CVS.

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 HBA1 & HBA2 gene deletion. It is commonly used with the system or sample type Amnio fld/CVS.

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

  • HBA1 and HBA2 gene deletion in Amniotic fluid or Chorionic villus sample by Molecular genetics method
  • HBA1 & HBA2 gene deletion
  • Alpha-globin is an essential component of the hemoglobin tetramer, starting from the early stages of embryonic development. Deletion mutations involving one or both of the two alpha-globin genes (alpha1 and alpha2, located on chromosome 16p13) lead to reduced production of alpha-globin chains, and are the major cause of alpha-thalassemia. Severity of the disease is dependent on the total copy number of functional alpha-globin genes remaining. This assay detects the seven most common deletions (-alpha3.7, -alpha4.2, -alpha20.5, --SEA, --MED, -FIL, and --THAI) found in patients with alpha-thalassemia. This assay is performed by allele-specific PCR amplification of deletion mutation fragments, followed by agarose gel electrophoresis of the amplification products.
  • AF; alpha-2 globin; Amn; Amn fl; Amn/CVS; Amnio; Amniotic flu; Amniotic fluid; Chorionic villi; Chorionic villus sample; Del; Deletions; Document; Finding; Findings; HBA1 + HBA2; HBA-T2; HBH; Hemoglobin, alpha 2; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.DELDUP; PCR; Point in time; Random

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

HBA1 and HBA2 gene del Molgen Doc (Amnio fld/CVS)HBA1 and HBA2 gene deletion in Amniotic fluid or Chorionic villus sample by Molecular genetics methodHBA1 + HBA2 Del Amn/CVSHBA1 & HBA2 gene deletionMOLPATH.DELDUPHBA1 and HBA2 gene deletion analysis, Amnio Fld/CVSFind

Frequently asked questions

Code details

Code103844-7
SystemLOINC
Display nameHBA1 and HBA2 gene del Molgen Doc (Amnio fld/CVS)
DescriptionHBA1 & HBA2 gene deletion
Short nameHBA1 + HBA2 Del Amn/CVS
ComponentHBA1 & HBA2 gene deletion
PropertyFind
TimingPt
System (specimen)Amnio fld/CVS
ScaleDoc
MethodMolgen
ClassMOLPATH.DELDUP
StatusACTIVE
Order/ObservationBoth

Flags

BillableNo
Valid clinical useNo

Source

SourceLOINC
Version2.82
Releasemain
First released2.77
Last changed2.77

Consumer names

HBA1 and HBA2 gene deletion analysis, Amnio Fld/CVS

Part names

HBA1 & HBA2 gene deletionFindPtAmnio fld/CVSDocMolgenFindingPoint in time (spot)Amniotic fluid or Chorionic villus sampleMolecular 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.