AutoICD API

107252-9

Laboratory

CSF3R gene mutations found [Identifier] in Blood or Tissue by Sequencing Nominal

LOINC 6-Axis Classification

Component

CSF3R gene targeted mutation analysis

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Sequencing

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

CSF3R gene Mut Anl Bld/T Seq

Display Name

CSF3R gene targeted mutation analysis Sequencing Nom (Bld/Tiss)

Related Names

BloodCD114colony stimulating factor 3 receptorGCSFRhigh-throughput sequencingHTSIdentity or presenceMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNext generation sequencingNGSNominalPoint in timeRandomSCN7TissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 107252-9?

LOINC code 107252-9 identifies "CSF3R gene mutations found [Identifier] in Blood or Tissue by Sequencing Nominal". It measures CSF3R gene targeted mutation analysis in Bld/Tiss.

What does 107252-9 measure?

This code measures CSF3R 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.