LOINCActiveBoth

LOINC Code 90743-6: CYBB gene full & NCF1 gene c.75_76delGT analysis Molgen Doc (Bld/Tiss)

90743-6 is a LOINC code used to identify CYBB gene full & NCF1 gene c.75_76delGT analysis Molgen Doc (Bld/Tiss) 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 CYBB gene full & NCF1 gene c.75_76delGT analysis. It is commonly used with the system or sample type Bld/Tiss.

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 CYBB gene full & NCF1 gene c.75_76delGT analysis. It is commonly used with the system or sample type Bld/Tiss.

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

  • CYBB gene full and NCF1 gene c.75_76delGT analysis in Blood or Tissue by Molecular genetics method
  • CYBB gene full & NCF1 gene c.75_76delGT analysis
  • AMCBX2; Blood; CGD; CYBB full + NCF1 c.75_76delGT; CYBB gene full + NCF1 gene; cytochrome b-245, beta polypeptide; Cytochrome b-245, beta polypeptide (chronic granulomatous disease); Document; Finding; Findings; Genetics; GP91-1; GP91PHOX; GP91-PHOX; Heredity; Heritable; IMD34; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; NCF-1; NCF1A; NCF-47K; neutrophil cytosolic factor 1; Neutrophil cytosolic factor 1, (chronic granulomatous disease, autosomal 1); NOX2; NOXO2; p47phox; p91-PHOX; PCR; Point in time; Random; SH3PXD1A; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

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

CYBB gene full & NCF1 gene c.75_76delGT analysis Molgen Doc (Bld/Tiss)CYBB gene full and NCF1 gene c.75_76delGT analysis in Blood or Tissue by Molecular genetics methodCYBB full + NCF1 c.75_76delGT Bld/TCYBB gene full & NCF1 gene c.75_76delGT analysisMOLPATH.MUTCYBB gene Full & NCF1 gene C.75_76delGT Analysis, Blood or tissue specimenFind

Frequently asked questions

Code details

Code90743-6
SystemLOINC
Display nameCYBB gene full & NCF1 gene c.75_76delGT analysis Molgen Doc (Bld/Tiss)
DescriptionCYBB gene full & NCF1 gene c.75_76delGT analysis
Short nameCYBB full + NCF1 c.75_76delGT Bld/T
ComponentCYBB gene full & NCF1 gene c.75_76delGT analysis
PropertyFind
TimingPt
System (specimen)Bld/Tiss
ScaleDoc
MethodMolgen
ClassMOLPATH.MUT
StatusACTIVE
Order/ObservationBoth

Flags

BillableNo
Valid clinical useNo

Source

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

Consumer names

CYBB gene Full & NCF1 gene C.75_76delGT Analysis, Blood or tissue specimen

Part names

CYBB gene full & NCF1 gene c.75_76delGT analysisFindPtBld/TissDocMolgenCYBB gene full and NCF1 gene c.75_76delGT analysisFindingPoint in time (spot)Blood or TissueMolecular 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.