AutoICD API

35297-1

Laboratory

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

LOINC 6-Axis Classification

Component

LMNA 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

LMNA gene Mut Anl Bld/T

Display Name

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

Related Names

BloodCDCD1CDDCCharcot-Marie-Tooth disease, axonal, type 2B1CMD1ACMT2B1EMD2FPLFPLDFPLD2GeneticsHeredityHeritableHGPSIDCIdentity or presenceInheritedlamin A/CLDP1LFPLGMD1BLMN1LMNCLMNL1Molecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalPCRPoint in timePRO1Progeria 1 (Hutchinson-Gilford type)RandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 35297-1?

LOINC code 35297-1 identifies "LMNA gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures LMNA gene targeted mutation analysis in Bld/Tiss.

What does 35297-1 measure?

This code measures LMNA 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.