AutoICD API

91679-1

Laboratory

F8 gene intron 22 inversion targeted mutation analysis in Blood or Tissue by Molecular genetics method

LOINC 6-Axis Classification

Component

F8 gene intron 22 inversion targeted mutation analysis

Property

Find

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Doc

Method Type

Molgen

Details

Class

MOLPATH.INV

Order/Observation

Both

Short Name

F8 intron 22 Inv Mut Anl Bld/T

Display Name

F8 gene intron 22 inversion targeted mutation analysis Molgen Doc (Bld/Tiss)

Related Names

AHFBloodClassic hemophiliaCoagulation Factor VIII genecoagulation factor VIII, procoagulant componentDocumentDXS1253EF8 intron 22 InvF8BF8CFactor 8FindingFindingsFVIIIFVIII geneHaemophiliaHEMAHemophilia AMolecular geneticsMolecular pathologyMOLPATHMOLPATH.INVMutMut AnlMutationsPCRPoint in timeProcoagulant componentRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 91679-1?

LOINC code 91679-1 identifies "F8 gene intron 22 inversion targeted mutation analysis in Blood or Tissue by Molecular genetics method". It measures F8 gene intron 22 inversion targeted mutation analysis in Bld/Tiss.

What does 91679-1 measure?

This code measures F8 gene intron 22 inversion targeted mutation analysis in Bld/Tiss. It belongs to the MOLPATH.INV 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.