AutoICD API

41055-5

Laboratory

SLC26A4 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

SLC26A4 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

SLC26A4 gene Mut Anl Bld/T

Display Name

SLC26A4 gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

BloodDeafness, autosomal recessive 4DFNB4EVAGeneticsHeredityHeritableIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalNSRD4PCRPDSPendred syndromePendrin (Sodium-independent chloride/iodide transporter)Point in timeRandomsolute carrier family 26 (anion exchanger), member 4Solute carrier family 26, member 4TDH2BTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 41055-5?

LOINC code 41055-5 identifies "SLC26A4 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures SLC26A4 gene targeted mutation analysis in Bld/Tiss.

What does 41055-5 measure?

This code measures SLC26A4 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.