AutoICD API

81869-0

Laboratory

PRNP gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method

LOINC 6-Axis Classification

Component

PRNP gene mutation analysis limited to known familial mutations

Property

Find

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Doc

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

PRNP gene Fam Mut Anl Bld/T

Display Name

PRNP gene familial mut analysis Molgen Doc (Bld/Tiss)

Related Names

AltPrPASCRBloodCD230CJDDocumentFam Mut AnlFindingFindingsGeneticsGSSHeredityHeritableInheritedKURULMTEDLTDMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMutationMutationsMutsp27-30PCRPoint in timeprion proteinPrion protein genePRIPPrPPrP27-30PrP33-35CPrPcRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 81869-0?

LOINC code 81869-0 identifies "PRNP gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method". It measures PRNP gene mutation analysis limited to known familial mutations in Bld/Tiss.

What does 81869-0 measure?

This code measures PRNP gene mutation analysis limited to known familial mutations 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.