AutoICD API

41074-6

Laboratory

NPHS1 gene mutations found [Identifier] in Body fluid by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

NPHS1 gene targeted mutation analysis

Property

Prid

Time Aspect

Pt

System

Body fld

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

NPHS1 gene Mut Anl Fld

Display Name

NPHS1 gene targeted mutation analysis Molgen Nom (Body fld)

Related Names

B/FBFbodBodiesBody fluidBody fluid, unspCNFFlFldFLUFluidGeneticsHeredityHeritableIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNephrinnephrosis 1, congenital, Finnish typenephrosis 1, congenital, Finnish type (nephrin)NominalNPHNPCRPoint in timeRandom

Frequently Asked Questions

What is LOINC code 41074-6?

LOINC code 41074-6 identifies "NPHS1 gene mutations found [Identifier] in Body fluid by Molecular genetics method Nominal". It measures NPHS1 gene targeted mutation analysis in Body fld.

What does 41074-6 measure?

This code measures NPHS1 gene targeted mutation analysis in Body fld. It belongs to the MOLPATH.MUT class in the LOINC classification.

What is LOINC?

LOINC (Logical Observation Identifiers Names and Codes) is a universal standard for identifying laboratory and clinical observations. It is maintained by the Regenstrief Institute and used worldwide for health data exchange.