AutoICD API

101385-3

Laboratory

NF1 gene deletion+duplication and full mutation analysis in Blood or Tissue by Molecular genetics method

LOINC 6-Axis Classification

Component

NF1 gene deletion+duplication & full mutation analysis

Property

Find

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Doc

Method Type

Molgen

Details

Class

MOLPATH

Order/Observation

Both

Short Name

NF1 gene Del+Dup + Full Mut Anl Bld/T

Display Name

NF1 gene del+dup and full mutation analysis Molgen Doc (Bld/Tiss)

Related Names

AmplificationBloodDelDel+DupDel+Dup + Full Mut AnlDeletionsDocumentDpFindingFindingsfull gene sequencingFull Mut AnlMolecular geneticsMolecular pathologyMOLPATHMutMutationsNeurofibromatosisNeurofibromin 1NFNSPCRPoint in timeRandomsequencing of entire coding regionTissueTissue, unspecifiedvon Recklinghausen diseaseVRNFWatson diseaseWBWhole bloodWhole blood or TissueWSS

Frequently Asked Questions

What is LOINC code 101385-3?

LOINC code 101385-3 identifies "NF1 gene deletion+duplication and full mutation analysis in Blood or Tissue by Molecular genetics method". It measures NF1 gene deletion+duplication & full mutation analysis in Bld/Tiss.

What does 101385-3 measure?

This code measures NF1 gene deletion+duplication & full mutation analysis in Bld/Tiss. It belongs to the MOLPATH 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.