AutoICD API

101388-7

Laboratory

GP1BB full mutation analysis in Blood or Tissue by Molecular genetics method

LOINC 6-Axis Classification

Component

GP1BB gene full mutation analysis

Property

Find

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Doc

Method Type

Molgen

Details

Class

MOLPATH

Order/Observation

Both

Short Name

GP1BB Full Mut Anl Bld/T

Display Name

GP1BB full mutation analysis Molgen Doc (Bld/Tiss)

Related Names

Bernard Soulier syndromebeta polypeptideBloodCD42cDocumentFindingFindingsfull gene sequencingFull Mut AnlGP1BB full mutation analysisGPIbbetaMolecular geneticsMolecular pathologyMOLPATHMutMutationsPCRplatelet glycoprotein Ib beta chainPoint in timeRandomsequencing of entire coding regionTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 101388-7?

LOINC code 101388-7 identifies "GP1BB full mutation analysis in Blood or Tissue by Molecular genetics method". It measures GP1BB gene full mutation analysis in Bld/Tiss.

What does 101388-7 measure?

This code measures GP1BB gene full mutation analysis in Bld/Tiss. 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.