AutoICD API

41064-7

Laboratory

PYGM gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

PYGM gene targeted mutation analysis

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

PYGM gene Mut Anl Bld/T

Display Name

PYGM gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

BloodGeneticsGlycogen phosphorylase, muscle formGlycogen storage disease type VHeredityHeritableIdentity or presenceInheritedMcArdle syndromeMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsMyophosphorylase geneNominalPCRphosphorylase, glycogen, musclePoint in timeRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 41064-7?

LOINC code 41064-7 identifies "PYGM gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures PYGM gene targeted mutation analysis in Bld/Tiss.

What does 41064-7 measure?

This code measures PYGM gene targeted 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.