AutoICD API

70291-0

Laboratory

inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript [Presence] in Blood or Tissue by Molecular genetics method

Definition

This term is used to identify a leukemia causing inversion on chromosome 16 resulting in gene fusion between CBFB (16q22) and MYH11 (16p13) genes. The term was created for (but not limited to) DNA Technology's HemaVision HV01-28N kit, a qualitative in vitro diagnostic test for 28 leukemia causing chromosomal alterations including more than 80 breakpoints plus associated mRNA splice variants. Reverse transcription followed by multiplex nested polymerase chain reactions (RT-PCR) and agarose gel electrophoresis are used to identify gene fusions caused by chromosomal translocations, gene deletions or inversions. Testing information is useful for predicting development of the disease and selection of treatment.

LOINC 6-Axis Classification

Component

inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript

Property

Arb

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Ord

Method Type

Molgen

Details

Class

MOLPATH.INV

Order/Observation

Both

Short Name

inv(16)(p13;q22) Bld/T Ql

Display Name

inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript Molgen Ql (Bld/Tiss)

Related Names

Acute myeloid leukemiaAMLArbitraryBloodDNAgene fusiongene translocationinv(16)(CBFB,MYH11) gene inversioninv(16)(p13q22)Inversion 16Molecular geneticsMolecular pathologyMOLPATHMOLPATH.INVOrdinalPCRPoint in timeQLQualQualitativeRandomRNAScreenTissueTissue, unspecifiedtranslocationWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 70291-0?

LOINC code 70291-0 identifies "inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript [Presence] in Blood or Tissue by Molecular genetics method". This term is used to identify a leukemia causing inversion on chromosome 16 resulting in gene fusion between CBFB (16q22) and MYH11 (16p13) genes. The term was created for (but not limited to) DNA Technology's HemaVision HV01-28N kit, a qualitative in vitro diagnostic test for 28 leukemia causing chromosomal alterations including more than 80 breakpoints plus associated mRNA splice variants. Reverse transcription followed by multiplex nested polymerase chain reactions (RT-PCR) and agarose gel electrophoresis are used to identify gene fusions caused by chromosomal translocations, gene deletions or inversions. Testing information is useful for predicting development of the disease and selection of treatment.

What does 70291-0 measure?

This code measures inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript in Bld/Tiss. It belongs to the MOLPATH.INV 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.