AutoICD API

21672-1

Laboratory

F8 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

F8 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

F8 gene Mut Anl Bld/T

Display Name

F8 gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

AHFBloodClassic hemophiliaCoagulation Factor VIII genecoagulation factor VIII, procoagulant componentDXS1253EF8BF8CFactor 8FVIIIFVIII geneGeneticsHaemophiliaHEMAHemophilia AHeredityHeritableIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalPCRPoint in timeProcoagulant componentRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 21672-1?

LOINC code 21672-1 identifies "F8 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures F8 gene targeted mutation analysis in Bld/Tiss.

What does 21672-1 measure?

This code measures F8 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.