AutoICD API

41112-4

Laboratory

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

LOINC 6-Axis Classification

Component

CMT axonal 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

CMT2 gene Mut Anl Bld/T

Display Name

CMT axonal gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

Axonal HMSNBloodCharcot-Marie Tooth disease, type 2CMTCMT2CMT2 geneGeneticsGJB, MPZ and NEFL gene mutationsHeredityHeritableIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalPCRPoint in timeRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 41112-4?

LOINC code 41112-4 identifies "CMT axonal gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures CMT axonal gene targeted mutation analysis in Bld/Tiss.

What does 41112-4 measure?

This code measures CMT axonal 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.