105331-3

Laboratory

Hereditary bleeding disorders factor and von Willebrand multigene analysis in Specimen by Molecular genetics method

LOINC 6-Axis Classification

Component

Hereditary bleeding disorders factor and von Willebrand multigene analysis

Property

Find

Time Aspect

Pt

System

XXX

Scale Type

Doc

Method Type

Molgen

Details

Class

MOLPATH

Order/Observation

Order

Short Name

Hered bleed fact & Vw multi analy Spec

Display Name

Hereditary bleeding disorders factor and von Willebrand multigene analysis Molgen Doc (Specimen)

Related Names

DocumentFacFactFindingFindingsGeneGene panelHered bleed fact & Vw multi analyMiscMiscellaneousMolecular geneticsMolecular pathologyMOLPATHMulti-gene studyMultiple-gene panel testOtherPCRPoint in timeRandomSpecTo be specified in another part of the messageUnspecifiedVon willVonwillebrandvWf

Frequently Asked Questions

What is LOINC code 105331-3?

LOINC code 105331-3 identifies "Hereditary bleeding disorders factor and von Willebrand multigene analysis in Specimen by Molecular genetics method". It measures Hereditary bleeding disorders factor and von Willebrand multigene analysis in XXX.

What does 105331-3 measure?

This code measures Hereditary bleeding disorders factor and von Willebrand multigene analysis in XXX. 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.