AutoICD API

75386-3

Laboratory

MEN1 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method

LOINC 6-Axis Classification

Component

MEN1 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

MEN1 gene Fam Mut Anl Bld/T

Display Name

MEN1 gene familial mut analysis Molgen Doc (Bld/Tiss)

Related Names

BloodDocumentFam Mut AnlFindingFindingsGeneticsHeredityHeritableInheritedLMTEDLTDMEAIMeninMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSmultiple endocrine neoplasia IMultiple endocrine neoplasia type IMutMutationMutationsMutsPCRPoint in timeRandomSCG2TissueTissue, unspecifiedWBWermer syndromeWhole bloodWhole blood or TissueZollinger-Ellison syndrome

Frequently Asked Questions

What is LOINC code 75386-3?

LOINC code 75386-3 identifies "MEN1 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method". It measures MEN1 gene mutation analysis limited to known familial mutations in Bld/Tiss.

What does 75386-3 measure?

This code measures MEN1 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.