AutoICD API

94239-1

Laboratory

F11 gene full mutation analysis in Blood or Tissue by Sequencing

Definition

Full gene sequence analysis of the F11 gene to identify a pathogenic mutation associated with factor XI deficiency (FXID, Hemophilia C).[GHR gene: F11]

LOINC 6-Axis Classification

Component

F11 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

F11 Full Mut Anl Bld/T Seq

Display Name

F11 gene full mutation analysis Sequencing Doc (Bld/Tiss)

Related Names

BloodCoagulation factor XIDocumentFindingFindingsfull gene sequencingFull Mut AnlFXIGeneticsHeredityHeritablehigh-throughput sequencingHTSInheritedLemierre syndromeMolecular pathologyMOLPATHMutMutationsNext generation sequencingNGSPlasma thromboplastin antecedentPoint in timePTARandomsequencing of entire coding regionTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 94239-1?

LOINC code 94239-1 identifies "F11 gene full mutation analysis in Blood or Tissue by Sequencing". Full gene sequence analysis of the F11 gene to identify a pathogenic mutation associated with factor XI deficiency (FXID, Hemophilia C).[GHR gene: F11]

What does 94239-1 measure?

This code measures F11 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.