What does this LOINC code represent?

This LOINC code identifies a lab observation, measurement, question, or clinical concept in a standardized format.

Is this enough to understand my test result?

No. The code identifies the test or observation, but the interpretation depends on the actual result, reference range, and clinical context.

LOINCActiveBoth

LOINC Code 99967-2: Atypical hemolytic uremic syndrome multigene analysis Molgen Doc (Bld/Tiss)

Name: LOINC Code 99967-2: Atypical hemolytic uremic syndrome multigene analysis Molgen Doc (Bld/Tiss)
Creator: HealthAssure Clinical Team
Published: 2026-05-21T09:00:34.292Z

99967-2 is a LOINC code used to identify Atypical hemolytic uremic syndrome multigene 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 Atypical hemolytic uremic syndrome multigene 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 Atypical hemolytic uremic syndrome multigene 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

Atypical hemolytic uremic syndrome multigene analysis in Blood or Tissue by Molecular genetics method

Atypical hemolytic uremic syndrome multigene analysis

Multigene testing for atypical hemolytic uremic syndrome (aHUS), a condition that can begin in the neonatal period to adulthood and consists of hemolytic anemia, thrombocytopenia, and renal failure caused by platelet thrombi in the kidney and other organs. Genes associated with genetic aHUS include C3, C5, CD46, CFB, CFH, CFHR1, CFHR2, CFHR3, CFHR4, CFHR5, CFI, DGKE, PLG, THBD, and MMACHC. Testing is performed for diagnostic, prognostic, and therapeutic assessment in patients with aHUS.[NCBI BooksNBK1367]

aHUS multigene analysis; Atyp; Blood; Document; Finding; Findings; Gene; Gene panel; Molecular genetics; Molecular pathology; MOLPATH; Multi-gene study; Multiple-gene panel test; PCR; Point in time; Random; Reactive; 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

Atypical hemolytic uremic syndrome multigene analysis Molgen Doc (Bld/Tiss)Atypical hemolytic uremic syndrome multigene analysis in Blood or Tissue by Molecular genetics methodaHUS multigene analysis Bld/TAtypical hemolytic uremic syndrome multigene analysisMOLPATHAtypical hemolytic uremic syndrome multigene analysis, Blood or tissue specimenFind

Frequently asked questions

Code details

Code99967-2

SystemLOINC

Display nameAtypical hemolytic uremic syndrome multigene analysis Molgen Doc (Bld/Tiss)

DescriptionAtypical hemolytic uremic syndrome multigene analysis

Short nameaHUS multigene analysis Bld/T

ComponentAtypical hemolytic uremic syndrome multigene analysis

PropertyFind

TimingPt

System (specimen)Bld/Tiss

ScaleDoc

MethodMolgen

ClassMOLPATH

StatusACTIVE

Order/ObservationBoth

Flags

BillableNo

Valid clinical useNo

Source

SourceLOINC

Version2.82

Releasemain

First released2.72

Last changed2.72

Consumer names

Atypical hemolytic uremic syndrome multigene analysis, Blood or tissue specimen

Part names

Atypical hemolytic uremic syndrome multigene analysisFindPtBld/TissDocMolgenFindingPoint 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.