AutoICD API

94225-0

Laboratory

TTR gene full mutation analysis in Blood or Tissue by Sequencing

Definition

Full gene sequence analysis, including all coding regions and intron/exon boundaries, of the TTR gene for the diagnosis of transthyretin-associated familial amyloidosis, the most common hereditary amyloidosis.

LOINC 6-Axis Classification

Component

TTR gene full mutation analysis

Property

Find

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Doc

Method Type

Sequencing

Details

Class

MOLPATH

Order/Observation

Both

Short Name

TTR gene Full Mut Anl Bld/T Seq

Display Name

TTR gene full mutation analysis Sequencing Doc (Bld/Tiss)

Related Names

BloodCTSCTS1DocumentFindingFindingsfull gene sequencingFull Mut AnlGeneticsHEL111HeredityHeritablehigh-throughput sequencingHsT2651HTSInheritedMolecular pathologyMOLPATHMutMutationsNext generation sequencingNGSPALBPoint in timeRandomsequencing of entire coding regionTBPATissueTissue, unspecifiedtransthyretinTransthyretin (prealbumin, amyloidosis type I) geneWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 94225-0?

LOINC code 94225-0 identifies "TTR gene full mutation analysis in Blood or Tissue by Sequencing". Full gene sequence analysis, including all coding regions and intron/exon boundaries, of the TTR gene for the diagnosis of transthyretin-associated familial amyloidosis, the most common hereditary amyloidosis.

What does 94225-0 measure?

This code measures TTR gene full mutation analysis 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.