AutoICD API

94238-3

Laboratory

F12 gene full mutation analysis in Blood or Tissue by Sequencing

Definition

Full gene sequence analysis of the F12 gene to identify a pathogenic mutation associated with factor XII deficiency or hereditary angioedema with normal C1 inhibitor (FXII-HAE).[GHR gene: F12]

LOINC 6-Axis Classification

Component

F12 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

F12 gene Full Mut Anl Bld/T Seq

Display Name

F12 gene full mutation analysis Sequencing Doc (Bld/Tiss)

Related Names

beta-factor XIIa part 1Bloodcoagulation factor XIIcoagulation factor XII (Hageman factor)coagulation factor XIIa heavy chaincoagulation factor XIIa light chainDocumentEC 3.4.21.38FindingFindingsfull gene sequencingFull Mut AnlGeneticsHAE3HAEXHAFHageman factorHeredityHeritablehigh-throughput sequencingHTSInheritedMolecular pathologyMOLPATHMutMutationsNext generation sequencingNGSPoint in timeRandomsequencing of entire coding regionTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 94238-3?

LOINC code 94238-3 identifies "F12 gene full mutation analysis in Blood or Tissue by Sequencing". Full gene sequence analysis of the F12 gene to identify a pathogenic mutation associated with factor XII deficiency or hereditary angioedema with normal C1 inhibitor (FXII-HAE).[GHR gene: F12]

What does 94238-3 measure?

This code measures F12 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.