AutoICD API

35379-7

Laboratory

HNPCC genes mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

HNPCC genes 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

HNPCC genes Mut Anl Bld/T

Display Name

HNPCC genes targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

BloodCOCA2FCC2GeneticsHereditary Nonpolyposis Colorectal CancerHeredityHeritablehMLH1HNPCCHNPCC2Identity or presenceInheritedLynch syndromeMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsmutL homolog 1NominalPCRPoint in timeRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 35379-7?

LOINC code 35379-7 identifies "HNPCC genes mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures HNPCC genes targeted mutation analysis in Bld/Tiss.

What does 35379-7 measure?

This code measures HNPCC genes 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.