AutoICD API

77627-8

Laboratory

HBB gene mutations found [Identifier] in Blood or Tissue by Sequencing Nominal

LOINC 6-Axis Classification

Component

HBB gene full mutation analysis

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Sequencing

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

HBB gene Full Mut Anl Bld/T Seq

Display Name

HBB gene full mutation analysis Sequencing Nom (Bld/Tiss)

Related Names

Beta globulin geneBeta thalessemiabeta-globinBloodCD113t-Cfull gene sequencingFull Mut AnlGeneticsHemoglobin beta chainHemoglobin S genehemoglobin, betaHeredityHeritablehigh-throughput sequencingHTSIdentity or presenceInheritedMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMutationsNext generation sequencingNGSNominalPoint in timeRandomsequencing of entire coding regionSickle cell anemiaTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 77627-8?

LOINC code 77627-8 identifies "HBB gene mutations found [Identifier] in Blood or Tissue by Sequencing Nominal". It measures HBB gene full mutation analysis in Bld/Tiss.

What does 77627-8 measure?

This code measures HBB gene full 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.