AutoICD API

105336-2

Laboratory

Hereditary thrombosis disorders multigene analysis in Blood by Molecular genetics method

LOINC 6-Axis Classification

Component

Hereditary thrombosis disorders multigene analysis

Property

Find

Time Aspect

Pt

System

Bld

Scale Type

Doc

Method Type

Molgen

Details

Class

MOLPATH

Order/Observation

Order

Short Name

Hered throm dis multi analy Bld

Display Name

Hereditary thrombosis disorders multigene analysis Molgen Doc (Bld)

Related Names

BloodDocumentFindingFindingsGeneGene panelHered throm dis multi analyMolecular geneticsMolecular pathologyMOLPATHMulti-gene studyMultiple-gene panel testPCRPoint in timeRandomWBWhole blood

Frequently Asked Questions

What is LOINC code 105336-2?

LOINC code 105336-2 identifies "Hereditary thrombosis disorders multigene analysis in Blood by Molecular genetics method". It measures Hereditary thrombosis disorders multigene analysis in Bld.

What does 105336-2 measure?

This code measures Hereditary thrombosis disorders 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.