AutoICD API

77117-0

Laboratory

RPGRIP1 gene full mutation analysis in Blood or Tissue by Sequencing

LOINC 6-Axis Classification

Component

RPGRIP1 gene full mutation analysis

Property

Find

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Doc

Method Type

Sequencing

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

RPGRIP1 Full Mut Anl Bld/T Seq

Display Name

RPGRIP1 gene full mutation analysis Sequencing Doc (Bld/Tiss)

Related Names

BloodCongenital blindnessCORD13DocumentFindingFindingsfull gene sequencingFull Mut AnlGeneticsHeredityHeritablehigh-throughput sequencingHTSInheritedLCA6Molecular pathologyMOLPATHMOLPATH.MUTATIONSMutMutationsNext generation sequencingNGSPoint in timeRandomRetinitis pigmentosaretinitis pigmentosa GTPase regulator interacting protein 1RGI1RGRIPRPGRIPRPGRIP1dsequencing of entire coding regionTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 77117-0?

LOINC code 77117-0 identifies "RPGRIP1 gene full mutation analysis in Blood or Tissue by Sequencing". It measures RPGRIP1 gene full mutation analysis in Bld/Tiss.

What does 77117-0 measure?

This code measures RPGRIP1 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.