AutoICD API

42785-6

Laboratory

FGFR1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

FGFR1 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

FGFR1 gene Mut Anl Bld/T

Display Name

FGFR1 gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

Basic fibroblast growth factor receptor 1 precursorBFGFRbFGF-R-1BloodCD331CEKC-FGRFGFBRFGFR-1fibroblast growth factor receptor 1fibroblast growth factor receptor 1 (fms-related tyrosine kinase 2, Pfeiffer syndrome)FLGFLT2FLT-2GeneticsH2H3H4H5HBGFRHeredityHeritableHH2HRTFDSIdentity or presenceInheritedKAL2Molecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalN-SAMOGDPCRPoint in timeRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 42785-6?

LOINC code 42785-6 identifies "FGFR1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures FGFR1 gene targeted mutation analysis in Bld/Tiss.

What does 42785-6 measure?

This code measures FGFR1 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.