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Part Description

LP19837-1   t(14;18)(q32;q21.3)(IGH,BCL2)
Chromosomal translocation t(14;18)(q32;q21.3) IGH-BCL2 is found in follicular lymphomas (80-90%), diffuse large cell lymphomas (30%), and rarely in other lymphoproliferative disorders. It mainly occurs in B- cell non-hodgkin's lymphoma (NHL). This translocation is cytogenetically indistinguishable from t(14;18)(q32;q21) IGH-MALT1.[Atlas Genetics Oncology: t1418ID2006] FISH with probes specific to the targeted genes distinguishs between the two different rearrangements. Source: Regenstrief LOINC, t(14;18)(q32;q21) IGH/BCL2

LOINC Names Get Info

Fully-Specified Name
t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript minor break points:Arb:Pt:CSF:Ord:Molgen
Long Common Name
t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript minor break points [Presence] in Cerebrospinal Fluid by Molecular genetics method
Short Name
t(14;18)(IGH,BCL2) Minor CSF Ql
Display Name
t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript minor break points Molgen Ql (CSF)
Consumer Name Alpha Get Info
t(14;18)(q32;q21.3)(IGH,BCL2) minor break point analysis, Spinal fluid

Part Model Get Info

  • Component
    t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript minor break points
    LP19839-7
    • Analyte
      t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript minor break points
      LP19839-7
      • Component Numerator
        t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript minor break points
        LP19839-7
        • Component Numerator Core
          t(14;18)(q32;q21.3)(IGH,BCL2)
          LP19837-1
        • Component Numerator Core Suffix
          fusion transcript minor break points
          LP150245-1
      • Component Denominator
        NULL
         
        • Component Denominator Core
          NULL
           
        • Component Denominator Core Suffix
          NULL
           
    • Challenge
      NULL
       
    • Adjustment
      NULL
       
    • Count
      NULL
       
  • Property
    Arb
    LP6781-1
  • Time
    Pt
    LP6960-1
  • System
    CSF
    LP7156-5
    • System Core
      CSF
      LP7156-5
    • Super System
      NULL
       
  • Scale
    Ord
    LP7751-3
  • Method
    Molgen
    LP6404-0

Basic Attributes

Class
MOLPATH.TRNLOC
Type
Laboratory
First Released
Version 2.38
Last Updated
Version 2.83 (MIN)
Change Reason
Updated Component part to harmonize with ISCN guidelines and current LOINC nomenclature.
Order vs. Observation
Both

Language Variants Get Info

TagLanguageTranslation
cs-CZCzech (Czechia)Fúzní transkript t(14;18)(q32;q21.3)(IGH,BCL2) drobné body zlomu:Arbitrární:Časový bod:Mozkomíšní mok:Ordinální:Molekulární genetika
el-GRGreek (Greece)t(14;18)(q32;q21.3)(IGH,BCL2) ελάσσονα σημεία διακοπής μεταγραφών συγχώνευσης:Arb:Pt:ΕΝΥ:Ord:Μοριακή γενετική
Synonyms: Arb BCL2 MOLPATH MOLPATH.TRNLOC Ord Pt t(14;18)(q32;q21.3)(IGH,BCL2) ελάσσονα σημεία διακοπής μεταγραφών συγχώνευσης ΕΝΥ μεταγραφή συγχώνευσης Μοριακή γενετική
es-ESSpanish (Spain)t(14;18)(q32;q21.3)(IGH,BCL2) punto de rotura menor del transcrito de fusion:Arbitrario:Punto temporal:Líquido Cefalorraquideo:Ord:Genética molecular
es-MXSpanish (Mexico)t (14; 18) (q32; q21.3) (IGH, BCL2) puntos de ruptura menores de la transcripción de fusión:Arbitrario:Punto temporal:Fluído espinal cerebral:Ordinal:Genética molecular
fr-FRFrench (France)t(14;18)(q32;q21.3)(IGH,BCL2) transcrit de fusion point de rupture mineur:Arbitraire:Ponctuel:Liquide céphalorachidien:Qualitatif:Biologie moléculaire
it-ITItalian (Italy)t(14,18)(q32,q21.3)(IGH,BCL2), punti di rottura secondari di trascritto di fusione:Arb:Pt:LCS:Ord:Molgen
Synonyms: Arbitrario Genetica molecolare Liquido cerebrospinale Patologia molecolare Punti di rottura minori della traslocazione t(14,18)(IGH,BCL2) Punto nel tempo (episodio) Traslocazione genetica
nl-NLDutch (Netherlands)t(14;18)(q32;q21.3)(IGH,BCL2) fusietranscript minor breakpoints:aanwezigheid:moment:liquor cerebrospinalis:ordinaal:moleculair genetisch onderzoek
Synonyms: molgen
pl-PLPolish (Poland)t (14; 18) (q32; q21.3) (IGH,BCL2) mniejsze punkty przerwania transkryptu fuzyjnego:jednostka umowna:punkt w czasie:płyn mózgowo-rdzeniowy:uporządkowany:genetyka molekularna
Synonyms: diagnostyka molekularna Translokacja (14; 18) (q32; q21.3) (IGH,BCL2) Translokacja (14; 18) (q32; q21.3) (IGH,BCL2) mniejsze punkty przerwania transkryptu genu fuzyjnego Translokacja(14; 18) (q32; q21.3) (IGH,BCL2) transkrypt genu fuzyjnego
ru-RURussian (Russian Federation)t(14;18)(q32;q21.3)(IGH,BCL2) слияния транскрипт minor break points:Произв:ТчкВрм:ЦСЖ:Пор:МолГен
Synonyms: Порядковый Произвольный слияния транскрипт минорная точка разрыва Точка во времени;Момент химерная РНК, закодированная слитым геном Цереброспинальная жидкость
tr-TRTurkish (Turkey)t(14;18)(q32;q21.3)(IGH,BCL2) füzyon transkript minor kırılma noktaları:Sç:Zmlı:BOS:Srl:Molgen
zh-CNChinese (China)t(14;18)(q32;q21.3)(IGH,BCL2) 融合转录物次要断裂点:任意型:时间点:脑脊液:序数型:分子遗传学类实验室方法
Synonyms: BCL-2;B-细胞白血病/淋巴瘤 2;B细胞白血病/淋巴瘤2 CSF CSF;脊髓液;Cerebral spinal fluid;脑脊髓液 MCR T(14,18)(IGH,BCL2) 基因易位;T(14,18)(IGH,BCL2) 易位 T(14,18)(IGH,BCL2) 基因易位次要断裂点 任意;任意的;人工型 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 分子病理学.基因易位;分子病理学.易位;分子病理学试验.基因易位;分子病理学试验.易位;分子病理学试验类.易位;基因易位 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 时刻;随机;随意;瞬间 次断点 次断点类 次断裂点类 次要丛集区 次要丛集区域 次要断点 次要断点类 次要断裂点 次要断裂点类 次要簇集区 次要簇集区域 次要集中区 次要集中区（Minor Cluster Region，MCR） 次要集中区域 脊液 脊髓液 脑脊液（Cerebral spinal fluid，CSF） 脑脊髓液 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 融合转录物（转录本、转录产物、转录子、转录）次要断裂点;融合基因转录本次要断裂点;融合转录本次要断点

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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=60584-0