AutoICD API

95786-0

Laboratory

Gene XXX mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method

Definition

Carrier or diagnostic testing for at-risk relatives of an affected individual who has a previously identified known genetic mutation. Mutation analysis only includes testing for the known familial mutation(s). To report the gene(s) tested, use Gene studied [ID] [LOINC: 48018-6]. To report the specific variant(s) tested, use the gene mutations tested term [LOINC: 36908-2].

LOINC 6-Axis Classification

Component

Gene XXX mutation analysis limited to known familial mutations

Property

Find

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Doc

Method Type

Molgen

Details

Class

MOLPATH

Order/Observation

Both

Short Name

Gene XXX Fam Mut Anl Bld/T

Display Name

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

Related Names

BloodDocumentFam Mut AnlFindingFindingsGeneticsHeredityHeritableInheritedLMTEDLTDMolecular geneticsMolecular pathologyMOLPATHMutMutationMutationsMutsPCRPoint in timeRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 95786-0?

LOINC code 95786-0 identifies "Gene XXX mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method". Carrier or diagnostic testing for at-risk relatives of an affected individual who has a previously identified known genetic mutation. Mutation analysis only includes testing for the known familial mutation(s). To report the gene(s) tested, use Gene studied [ID] [LOINC: 48018-6]. To report the specific variant(s) tested, use the gene mutations tested term [LOINC: 36908-2].

What does 95786-0 measure?

This code measures Gene XXX mutation analysis limited to known familial mutations 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.