Version 2.76

Part Description

LP146062-7   inv(16)(p13.1;q22.1)(MYH11,CBFB)
The inv(16)(p13.1;q22.1) CBFB-MYH11 fusion transcript is a chromosomal abnormality associated with acute myelomonocytic leukemia (AML). This results in the formation of a chimeric protein between core binding factor beta and smooth muscle myosin heavy chain 11. Positive results are indicative of AML subtype M4E0. Source: Regenstrief LOINC

Fully-Specified Name

Component
inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript
Property
PrThr
Time
Pt
System
Bone mar
Scale
Ord
Method
Molgen

Additional Names

Short Name
inv(16)(p13;q22) Mar Ql
Display Name
inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript Molgen Ql (BM)
Consumer Name Alpha Get Info
inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript analysis, Bone marrow

Example Answer List: LL360-9

Source: Regenstrief Institute
Answer Code Score Answer ID
PositiveCopyright http://snomed.info/sct ID:10828004 Positive (qualifier value) LA6576-8
NegativeCopyright http://snomed.info/sct ID:260385009 Negative (qualifier value) LA6577-6

Basic Attributes

Class
MOLPATH.INV
Type
Laboratory
First Released
Version 2.48
Last Updated
Version 2.56
Change Reason
The PrThr property is used for LOINC terms whose results are reported using an ordered categorical scale, regardless of whether or not an internal threshold was used to make that determination. This change was approved by the Laboratory LOINC Committee in June 2016.
Order vs. Observation
Both

Language Variants Get Info

Tag Language Translation
es-ES Spanish (Spain) inv(16)(p13.1;q22.1)(MYH11,CBFB) Tránscritos de fusión:PrThr:Punto temporal:Médula ósea:Ord:Genética molecular
es-MX Spanish (Mexico) transcripción de fusión inv (16) (p13.1; q22.1) (MYH11, CBFB):Presencia o umbral:Punto temporal:Médula ósea:Ordinal:Genética molecular
fr-CA French (Canada) inv(16)(p13.1;q22.1)(MYH11,CBFB) transcrit de fusion:Présence-Seuil:Temps ponctuel:Moelle osseuse:Ordinal:Molgen
fr-FR French (France) inv(16)(p13.1;q22.1)(MYH11,CBFB) transcrit de fusion:Présence/Seuil:Ponctuel:Moelle osseuse:Qualitatif:Biologie moléculaire
it-IT Italian (Italy) inv(16)(p13.1;q22.1)(MYH11,CBFB) , trascritto di fusione:PrThr:Pt:Mid oss:Ord:Molgen
Synonyms: Genetica molecolare Inversione genetica Midollo osseo Patologia molecolare Presenza o Soglia Punto nel tempo (episodio)
nl-NL Dutch (Netherlands) inv(16)(p13.1;q22.1)(MYH11,CBFB) fusietranscript:aanwezigheid:moment:beenmerg:ordinaal:moleculair genetisch onderzoek
Synonyms: molgen
pt-BR Portuguese (Brazil) inv(16)(p13.1;q22.1)(MYH11,CBFB) transcrição de fusão::Pt:MedOssea:Ord:Genética molecular
ru-RU Russian (Russian Federation) inv(16)(p13.1;q22.1)(MYH11,CBFB) слияния транскрипт:PrThr:ТчкВрм:Костный мозг:Пор:МолГен
Synonyms: Порядковый Точка во времени;Момент химерная РНК, закодированная слитым геном
tr-TR Turkish (Turkey) inv(16)(p13.1;q22.1)(MYH11,CBFB) füzyon transkript:MevcEşik:Zmlı:Kem il:Srl:Molgen
Synonyms: Mevcut
zh-CN Chinese (China) inv(16)(p13.1;q22.1)(MYH11,CBFB) 融合转录物:存在情况或阈值:时间点:骨髓:序数型:分子遗传学类实验室方法
Synonyms: 依次型;分类顺序型;定性的;序数型(或称等级型);性质上的;有序型;有序性分类应答;有序性分类结果;秩次型;等级型;筛查;顺序型 倒位(16)(p13.1;q22.1)(MYH11,CBFB);基因倒位;基因倒置;倒位;倒置;gene inversion 分子病理学.基因倒位;分子病理学试验.基因倒位;分子病理学试验类.倒位 分子病理学;分子病理学试验 分子遗传学;分子遗传学方法;分子遗传学类方法;分子遗传学类检验方法;包括 RFL、PCR 及其他方法在内,用于在分子基础上检测遗传属性的方法的大类;聚合酶链反应;聚合酶链式反应 存在情况;存在;存在与否;是否存在;阈值;界值;界限;阀值;临界值;存在情况(存在、存在与否、是否存在)或阈值(界值、界限、阀值、临界值) 时刻;随机;随意;瞬间 融合转录物(转录本、转录产物、转录子、转录);融合基因转录本;融合转录 骨骼;骨头 髓

LOINC Terminology Service (API) using HL7® FHIR® Get Info

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=75010-9