AutoICD API

49857-6

Laboratory

SMN1 gene+SMN2 gene targeted mutation analysis in Blood or Tissue by Molecular genetics method

LOINC 6-Axis Classification

Component

SMN1 gene+SMN2 gene targeted mutation analysis

Property

Find

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Doc

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

SMN1+SMN2 gene Mut Anl Bld/T

Display Name

SMN1 gene+SMN2 gene targeted mutation analysis Molgen Doc (Bld/Tiss)

Related Names

BCD541BloodC-BCD541DocumentFindingFindingsGemin 1GEMIN1Gemin-1GeneticsHeredityHeritableInheritedKugelberg-Welander diseaseMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsPCRPoint in timeRandomSMASMA geneSMA@SMA1SMA2SMA3SMA4SMNSMN1+SMN2 geneSMNCSMNTSMVspinal muscular atrophySurvival motor neuron protein genesurvival of motor neuron 1, telomericsurvival of motor neuron 2, centromericT-BCD541TDRD16ATDRD16BTissueTissue, unspecifiedWBWerdnig-Hoffmann diseaseWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 49857-6?

LOINC code 49857-6 identifies "SMN1 gene+SMN2 gene targeted mutation analysis in Blood or Tissue by Molecular genetics method". It measures SMN1 gene+SMN2 gene targeted mutation analysis in Bld/Tiss.

What does 49857-6 measure?

This code measures SMN1 gene+SMN2 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.