AutoICD API

69484-4

Laboratory

FBN1 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method

Definition

This term is used for carrier or diagnostic testing for at-risk relatives of an affected individual who has a previously identified known genetic mutation within the FBN1 gene. Mutation analysis only includes testing for the known familial mutation(s).

LOINC 6-Axis Classification

Component

FBN1 gene mutation analysis limited to known familial mutations

Property

Find

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Doc

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

FBN1 gene Fam Mut Anl Bld/T

Display Name

FBN1 gene familial mut analysis Molgen Doc (Bld/Tiss)

Related Names

ACMICDBloodDocumentECTOL1Fam Mut AnlFBNfibrillin 1Fibrillin 1 (Marfan syndrome)FindingFindingsGeneticsGPHYSD2HeredityHeritableInheritedLMTEDLTDMASSMFS1Molecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMutationMutationsMutsOCTDPCRPoint in timeRandomSGSSSKSTissueTissue, unspecifiedWBWeill-Marchesani syndromeWhole bloodWhole blood or TissueWMSWMS2

Frequently Asked Questions

What is LOINC code 69484-4?

LOINC code 69484-4 identifies "FBN1 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method". This term is used for carrier or diagnostic testing for at-risk relatives of an affected individual who has a previously identified known genetic mutation within the FBN1 gene. Mutation analysis only includes testing for the known familial mutation(s).

What does 69484-4 measure?

This code measures FBN1 gene mutation analysis limited to known familial mutations 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.