AutoICD API

81866-6

Laboratory

MYH7 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method

LOINC 6-Axis Classification

Component

MYH7 gene mutation analysis limited to known familial mutations

Property

Find

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Doc

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

MYH7 Fam Mut Anl Bld/T

Display Name

MYH7 gene familial mut analysis Molgen Doc (Bld/Tiss)

Related Names

BloodCMD1SCMH1DocumentFam Mut AnlFindingFindingsGeneticsHeredityHeritableInheritedLMTEDLTDMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMPD1MutMutationMutationsMutsMYHCBmyosin, heavy chain 7, cardiac muscle, betaPCRPoint in timeRandomSPMDSPMMTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 81866-6?

LOINC code 81866-6 identifies "MYH7 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method". It measures MYH7 gene mutation analysis limited to known familial mutations in Bld/Tiss.

What does 81866-6 measure?

This code measures MYH7 gene mutation analysis limited to known familial mutations 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.