AutoICD API

36912-4

Laboratory

CATCH22 syndrome gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

CATCH22 syndrome gene mutations tested for

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Observation

Short Name

CATCH22 gene Mut Tested Bld/T

Display Name

CATCH22 syndrome gene mutations tested for Molgen Nom (Bld/Tiss)

Related Names

BloodCATCH22 geneDGSDiGeorge SyndromeGene mut testedGeneticsHeredityHeritableIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut TestedMutationMutsNominalPCRPoint in timeRandomShprintzen syndromeTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 36912-4?

LOINC code 36912-4 identifies "CATCH22 syndrome gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal". It measures CATCH22 syndrome gene mutations tested for in Bld/Tiss.

What does 36912-4 measure?

This code measures CATCH22 syndrome gene mutations tested for 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.