AutoICD API

47974-1

Laboratory

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

LOINC 6-Axis Classification

Component

THRB 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

THRB gene Mut Anl Bld/T

Display Name

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

Related Names

BloodC-ERBA-2C-ERBA-BETAERBA2ERBA-BETAGeneticsGRTHHeredityHeritableIdentity or presenceInheritedMGC126109MGC126110Molecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalNR1A2PCRPoint in timePRTHRandomTHR1THRB1THRB2Thyroid hormone receptor beta-1Thyroid hormone receptor beta-2thyroid hormone receptor, betaTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 47974-1?

LOINC code 47974-1 identifies "THRB gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures THRB gene targeted mutation analysis in Bld/Tiss.

What does 47974-1 measure?

This code measures THRB 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.