AutoICD API

94222-7

Laboratory

SERPINA1 gene full mutation analysis in Blood or Tissue by Sequencing

Definition

Full gene sequence analysis to identify a mutation within the coding regions and intron/exon boundaries of the SERPINA1 gene. Testing is performed for the diagnosis of Alpha-1-antitrypsin (A1A), particularly when a low or deficient alpha-1-antitrypsin serum levels is not explained by routine testing.

LOINC 6-Axis Classification

Component

SERPINA1 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

SERPINA1 gene Full Mut Anl Bld/T Seq

Display Name

SERPINA1 gene full mutation analysis Sequencing Doc (Bld/Tiss)

Related Names

A1AA1ATAATAlpha-1-antitrypsin deficiencyalpha1ATAnti-elastase geneBloodDocumentFindingFindingsfull gene sequencingFull Mut AnlGeneticsHeredityHeritablehigh-throughput sequencingHTSInheritedMolecular pathologyMOLPATHMutMutationsNext generation sequencingNGSPIPI1Point in timePRO2275Protease inhibitor 1Randomsequencing of entire coding regionSerine (or cysteine) proteinase inhibitorserpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1TissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 94222-7?

LOINC code 94222-7 identifies "SERPINA1 gene full mutation analysis in Blood or Tissue by Sequencing". Full gene sequence analysis to identify a mutation within the coding regions and intron/exon boundaries of the SERPINA1 gene. Testing is performed for the diagnosis of Alpha-1-antitrypsin (A1A), particularly when a low or deficient alpha-1-antitrypsin serum levels is not explained by routine testing.

What does 94222-7 measure?

This code measures SERPINA1 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.