AutoICD API

41075-3

Laboratory

NPHS1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

NPHS1 gene targeted mutation analysis

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

NPHS1 gene Mut Anl Bld/T

Display Name

NPHS1 gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

BloodCNFGeneticsHeredityHeritableIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsnephrinnephrosis 1, congenital, Finnish typenephrosis 1, congenital, Finnish type (nephrin)NominalNPHNPCRPoint in timeRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 41075-3?

LOINC code 41075-3 identifies "NPHS1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures NPHS1 gene targeted mutation analysis in Bld/Tiss.

What does 41075-3 measure?

This code measures NPHS1 gene targeted mutation analysis in Bld/Tiss. 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.