AutoICD API

21735-6

Laboratory

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

LOINC 6-Axis Classification

Component

SNCA 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

SNCA gene Mut Anl Bld/T

Display Name

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

Related Names

BloodGeneticsHeredityHeritableIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNACPNominalNon A4 component of amyloid precursorPARK1PARK4Parkinson diseasePCRPD1Point in timeRandomSynuclein, alphasynuclein, alpha (non A4 component of amyloid precursor)TissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 21735-6?

LOINC code 21735-6 identifies "SNCA gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures SNCA gene targeted mutation analysis in Bld/Tiss.

What does 21735-6 measure?

This code measures SNCA 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.