AutoICD API

111768-8

Laboratory

SMN1 gene copy number in Blood or Tissue by Molecular genetics method

LOINC 6-Axis Classification

Component

SMN1 gene copy number

Property

EntNum

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Qn

Method Type

Molgen

Details

Class

MOLPATH

Order/Observation

Both

Short Name

SMN1 gene copy number EntNum Bld/T

Display Name

SMN1 gene copy number Molgen (Bld/Tiss) [Entitic number]

Related Names

BCD541BloodEntiticEntitic numberGemin 1GEMIN1Kugelberg-Welander diseaseMolecular geneticsMolecular pathologyMOLPATHNoNumPCRPoint in timeQNTQuanQuantQuantitativeRandomSMASMA geneSMA@SMA1SMA2SMA3SMA4SMNSMNTSMVspinal muscular atrophySurvival motor neuron protein genesurvival of motor neuron 1, telomericT-BCD541TDRD16ATissueTissue, unspecifiedWBWerdnig-Hoffmann diseaseWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 111768-8?

LOINC code 111768-8 identifies "SMN1 gene copy number in Blood or Tissue by Molecular genetics method". It measures SMN1 gene copy number in Bld/Tiss.

What does 111768-8 measure?

This code measures SMN1 gene copy number in Bld/Tiss. It belongs to the MOLPATH 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.