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 34718-7: CFTR gene targeted mutation analysis Molgen Nom (Amn fld)

Name: LOINC Code 34718-7: CFTR gene targeted mutation analysis Molgen Nom (Amn fld)
Creator: HealthAssure Clinical Team
Published: 2026-05-21T08:59:22.387Z

34718-7 is a LOINC code used to identify CFTR gene targeted mutation analysis Molgen Nom (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 CFTR gene targeted mutation analysis. 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 CFTR gene targeted mutation analysis. 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

CFTR gene mutations found [Identifier] in Amniotic fluid by Molecular genetics method Nominal
CFTR gene targeted mutation analysis
ABC35; ABCC7; AF; Amn; Amn fl; Amnio; Amniotic flu; Amniotic fluid; CBAVD; CF; CFA; CFTR/MRP; Cystic fibrosis transmembrane conductance regulator; cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7); dJ760C5.1; Genetics; Gyn; Gynecology; Heredity; Heritable; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MRP7; Mut; Mut Anl; Mutations; Nominal; OB; ObGyn; Obstetrics; PCR; Point in time; Random; TNR-CFTR

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

CFTR gene targeted mutation analysis Molgen Nom (Amn fld)CFTR gene mutations found [Identifier] in Amniotic fluid by Molecular genetics method NominalCFTR Mut Anl AmnCFTR gene targeted mutation analysisMOLPATH.MUTCFTR gene targeted mutation analysis, Amniotic fluidPrid

Frequently asked questions

Code details

Code34718-7

SystemLOINC

Display nameCFTR gene targeted mutation analysis Molgen Nom (Amn fld)

DescriptionCFTR gene targeted mutation analysis

Short nameCFTR Mut Anl Amn

ComponentCFTR gene targeted mutation analysis

PropertyPrid

TimingPt

System (specimen)Amnio fld

ScaleNom

MethodMolgen

ClassMOLPATH.MUT

StatusACTIVE

Order/ObservationBoth

Flags

BillableNo

Valid clinical useNo

Source

SourceLOINC

Version2.82

Releasemain

First released2.11

Last changed2.73

Consumer names

CFTR gene targeted mutation analysis, Amniotic fluid

Part names

CFTR gene targeted mutation analysisPridPtAmnio fldNomMolgenPresence or IdentityPoint 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.