AutoICD API

21675-4

Laboratory

FGFR2 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

FGFR2 gene mutations tested for

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Observation

Short Name

FGFR2 gene Mut Tested Bld/T

Display Name

FGFR2 gene mutations tested for Molgen Nom (Bld/Tiss)

Related Names

Bacteria expressed kinaseBBDSBEKBFR-1BloodCD332CEK3CFD1Craniofacial dysostosis 1Crouzon syndromeECT1Fibroblast growth factor receptor 2Gene mut testedGeneticsHeredityHeritableIdentity or presenceInheritedJackson-Weiss syndromeJWSKeratinocyte growth factor receptorKGFRK-SAMKSAM-1Molecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut TestedMutationMutsNominalPCRPfeiffer syndromePoint in timeRandomTissueTissue, unspecifiedTK14TK25WBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 21675-4?

LOINC code 21675-4 identifies "FGFR2 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal". It measures FGFR2 gene mutations tested for in Bld/Tiss.

What does 21675-4 measure?

This code measures FGFR2 gene mutations tested for 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.