AutoICD API

51772-2

Laboratory

F9 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

F9 gene mutations tested for

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Observation

Short Name

F9 gene Mut Tested Bld/T

Display Name

F9 gene mutations tested for Molgen Nom (Bld/Tiss)

Related Names

BloodChristmas factorCoagulation Factor 9 genecoagulation factor IXCoagulation Factor IX geneFIXGene mut testedGeneticsHEMBHeredityHeritableIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut TestedMutationMutsNominalP19PCRPoint in timePTCRandomTHPH8TissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 51772-2?

LOINC code 51772-2 identifies "F9 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal". It measures F9 gene mutations tested for in Bld/Tiss.

What does 51772-2 measure?

This code measures F9 gene mutations tested for 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.