AutoICD API

21719-0

Laboratory

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

LOINC 6-Axis Classification

Component

NRAS 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

NRAS gene Mut Anl Bld/T

Display Name

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

Related Names

ALPS4BloodCMNSGeneticsHeredityHeritableIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNCMSneuroblastoma RAS viral (v-ras) oncogene homologNominalN-rasNRAS1NS6Oncogene NRASPCRPoint in timeRandomTissueTissue, unspecifiedv-ras neuroblastoma RAS viral oncogene homologWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 21719-0?

LOINC code 21719-0 identifies "NRAS gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures NRAS gene targeted mutation analysis in Bld/Tiss.

What does 21719-0 measure?

This code measures NRAS 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.