AutoICD API

51652-6

Laboratory

SLC14A1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

SLC14A1 gene targeted mutation analysis

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Observation

Short Name

SLC14A1 gene Mut Anl Bld/T

Display Name

SLC14A1 gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

BloodFLJ33745FLJ41687GeneticsHeredityHeritableHsT1341HUT11Identity or presenceInheritedJKKiddMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalPCRPoint in timeRACH1RACH2Randomsolute carrier family 14 (urea transporter), member 1 (Kidd blood group)TissueTissue, unspecifiedUT1UT-B1UTEWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 51652-6?

LOINC code 51652-6 identifies "SLC14A1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures SLC14A1 gene targeted mutation analysis in Bld/Tiss.

What does 51652-6 measure?

This code measures SLC14A1 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.