AutoICD API

94237-5

Laboratory

F2 gene full mutation analysis in Blood or Tissue by Sequencing

Definition

Full gene sequence analysis of the F2 gene to identify a pathogenic mutation associated with factor II (prothrombin) deficiency (F2D).[GHR gene: F2]

LOINC 6-Axis Classification

Component

F2 gene full mutation analysis

Property

Find

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Doc

Method Type

Sequencing

Details

Class

MOLPATH

Order/Observation

Both

Short Name

F2 gene Full Mut Anl Bld/T Seq

Display Name

F2 gene full mutation analysis Sequencing Doc (Bld/Tiss)

Related Names

BloodCoagulation Factor 2 genecoagulation factor II (thrombin)Coagulation Factor II geneDocumentFindingFindingsfull gene sequencingFull Mut AnlGeneticsHeredityHeritablehigh-throughput sequencingHTSInheritedMolecular pathologyMOLPATHMutMutationsNext generation sequencingNGSPoint in timeProthrombin geneProthrombin precursorPTRandomRPRGL2sequencing of entire coding regionTHPH1TissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 94237-5?

LOINC code 94237-5 identifies "F2 gene full mutation analysis in Blood or Tissue by Sequencing". Full gene sequence analysis of the F2 gene to identify a pathogenic mutation associated with factor II (prothrombin) deficiency (F2D).[GHR gene: F2]

What does 94237-5 measure?

This code measures F2 gene full mutation analysis in Bld/Tiss. It belongs to the MOLPATH 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.