AutoICD API

35466-2

Laboratory

AS+PWS gene targeted mutation analysis in Blood or Tissue by Molecular genetics method

LOINC 6-Axis Classification

Component

AS+PWS gene targeted mutation analysis

Property

Find

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Doc

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

AS+PWS gene Mut Anl Bld/T

Display Name

AS+PWS gene targeted mutation analysis Molgen Doc (Bld/Tiss)

Related Names

15q11-13Angelman + Prader Willi syndromeArterial StenosisBloodDocumentFindingFindingsGeneticsHeredityHeritableInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsPCRPoint in timePrader Willi syndromePrader-Willi syndrome chromosome regionPWSRandomSNRPNTissueTissue, unspecifiedUBE3AWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 35466-2?

LOINC code 35466-2 identifies "AS+PWS gene targeted mutation analysis in Blood or Tissue by Molecular genetics method". It measures AS+PWS gene targeted mutation analysis in Bld/Tiss.

What does 35466-2 measure?

This code measures AS+PWS 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.