AutoICD API

21676-2

Laboratory

FGFR3 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

FGFR3 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

FGFR3 gene Mut Anl Bld/T

Display Name

FGFR3 gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

ACHAchondroplasiaBloodCD333CEK2fibroblast growth factor receptor 3GeneticsHeredityHeritableHSFGFR3EXIdentity or presenceInheritedJTK4Molecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalPCRPoint in timeRandomThanatophoric dwarfismThanatophoric dysplasiaTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 21676-2?

LOINC code 21676-2 identifies "FGFR3 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures FGFR3 gene targeted mutation analysis in Bld/Tiss.

What does 21676-2 measure?

This code measures FGFR3 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.