LOINCActiveOrder

LOINC Code 105332-1: MYH9 gene full mutation analysis Molgen Doc (Bld)

105332-1 is a LOINC code used to identify MYH9 gene full mutation analysis Molgen Doc (Bld) 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 MYH9 gene full mutation analysis. It is commonly used with the system or sample type Bld.

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 MYH9 gene full mutation analysis. It is commonly used with the system or sample type Bld.

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: Order
  • Method: Molgen

What it does not mean

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

Key facts

  • MYH9 gene full mutation analysis in Blood by Molecular genetics method
  • MYH9 gene full mutation analysis
  • Blood; Document; Finding; Findings; full gene sequencing; Full Mut Anl; Molecular genetics; Molecular pathology; MOLPATH; Mut; Mutations; MYH9 gene full mut anl; Myosin heavy chain 9; PCR; Point in time; Random; sequencing of entire coding region; WB; Whole blood

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

MYH9 gene full mutation analysis Molgen Doc (Bld)MYH9 gene full mutation analysis in Blood by Molecular genetics methodMYH9 gene Full Mut Anl BldMYH9 gene full mutation analysisMOLPATHMYH9 gene variant analysis, BloodFind

Frequently asked questions

Code details

Code105332-1
SystemLOINC
Display nameMYH9 gene full mutation analysis Molgen Doc (Bld)
DescriptionMYH9 gene full mutation analysis
Short nameMYH9 gene Full Mut Anl Bld
ComponentMYH9 gene full mutation analysis
PropertyFind
TimingPt
System (specimen)Bld
ScaleDoc
MethodMolgen
ClassMOLPATH
StatusACTIVE
Order/ObservationOrder

Flags

BillableNo
Valid clinical useNo

Source

SourceLOINC
Version2.82
Releasemain
First released2.78
Last changed2.78

Consumer names

MYH9 gene variant analysis, Blood

Part names

MYH9 gene full mutation analysisFindPtBldDocMolgenFindingPoint in time (spot)BloodMolecular 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 105332-1 | HealthAssure