AutoICD API

96969-1

Laboratory

MYD88 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

MYD88 gene targeted mutation analysis

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

MYD88 Mut Anl Bld/T

Display Name

MYD88 gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

BloodIdentity or presenceIgM monoclonal gammopathy of undetermined significanceIgM-MGUSMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsMyD88 deficiencymyeloid differentiation primary response protein MyD88NominalPCRPoint in timeRandomTissueTissue, unspecifiedWaldenstroms MacroglobulinemiaWaldenstrom's MacroglobulinemiaWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 96969-1?

LOINC code 96969-1 identifies "MYD88 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures MYD88 gene targeted mutation analysis in Bld/Tiss.

What does 96969-1 measure?

This code measures MYD88 gene targeted mutation analysis 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.