AutoICD API

105333-9

Laboratory

Hereditary platelet function defect multigene analysis in Blood by Molecular genetics method

LOINC 6-Axis Classification

Component

Hereditary platelet function defect multigene analysis

Property

Find

Time Aspect

Pt

System

Bld

Scale Type

Doc

Method Type

Molgen

Details

Class

MOLPATH

Order/Observation

Order

Short Name

Hered plat func def multi analy Bld

Display Name

Hereditary platelet function defect multigene analysis Molgen Doc (Bld)

Related Names

BloodClosure timeClosure TmeDocumentFCNFindingFindingsFuncFunctGeneGene panelHered plat func def multi analyMolecular geneticsMolecular pathologyMOLPATHMulti-gene studyMultiple-gene panel testPCRPlPlateletsPlateltPltPoint in timeRandomThrombocyteThrombocytesWBWhole blood

Frequently Asked Questions

What is LOINC code 105333-9?

LOINC code 105333-9 identifies "Hereditary platelet function defect multigene analysis in Blood by Molecular genetics method". It measures Hereditary platelet function defect multigene analysis in Bld.

What does 105333-9 measure?

This code measures Hereditary platelet function defect multigene analysis in Bld. 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.