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Term Description

The detection by FISH analysis of gains (duplications, aneuploidy) and losses (deletion or monosomy) of chromosome regions (e.g. 1q, 13q, 9, 11 and 15) associated with multiple myeloma. This study is performed to determine the prognostic risk for disease outcome. For example, gains of chromosome 1q and monosomy or deletions of 13q are associated with less favorable outcomes whereas gains of chromosome 9, 11, and 15 are associated with more favorable outcomes.

Part Description

LP62864-1   FISH
FISH (fluorescence in situ hybridization) is a cytogenetic technique used to detect and localize the presence or absence of specific DNA sequences on chromosomes. FISH uses fluorescent probes that bind to only those parts of the chromosome with which they show a high degree of sequence similarity. Fluorescence microscopy can be used to find out where the fluorescent probe bound to the chromosomes. FISH is often used for finding specific features in DNA for use in genetic counseling, medicine, and species identification. FISH can also be used to detect and localize specific mRNAs within tissue samples. In this context, it can help define the spatial-temporal patterns of gene expression within cells and tissues. Copyright Text is available under the Creative Commons Attribution/Share-Alike License. See http://creativecommons.org/licenses/by-sa/3.0/ for details. Source: Wikipedia, FISH

LOINC Names Get Info

Fully-Specified Name
Chromosome 1q & 9 & 11 & 15 aneuploidy & chromosome region 13q deletion:Find:Pt:Bone mar:Doc:FISH
Long Common Name
Chromosome 1q and 9 and 11 and 15 aneuploidy and 13q deletion in Bone marrow by FISH
Short Name
Chr 1q+9+11+15 aneu 13q Del Mar FISH
Display Name
Chr 1q and 9 and 11 and 15 aneuploidy and 13q del FISH Doc (BM)
Consumer Name Alpha Get Info
Chromosome 1q and 9 and 11 and 15 aneuploidy and 13q deletion analysis, Bone marrow

Part Model Get Info

  • Component
    Chromosome 1q & 9 & 11 & 15 aneuploidy & chromosome region 13q deletion
    LP418223-6
    • Analyte
      Chromosome 1q & 9 & 11 & 15 aneuploidy & chromosome region 13q deletion
      LP418223-6
      • Component Numerator
        Chromosome 1q & 9 & 11 & 15 aneuploidy & chromosome region 13q deletion
        LP418223-6
        • Component Numerator Core
          Chromosome 1q & 9 & 11 & 15 aneuploidy & chromosome region 13q
          LP418230-1
        • Component Numerator Core Suffix
          deletion
          LP29253-9
      • Component Denominator
        NULL
         
        • Component Denominator Core
          NULL
           
        • Component Denominator Core Suffix
          NULL
           
    • Challenge
      NULL
       
    • Adjustment
      NULL
       
    • Count
      NULL
       
  • Property
    Find
    LP6813-2
  • Time
    Pt
    LP6960-1
  • System
    Bone mar
    LP7410-6
    • System Core
      Bone mar
      LP7410-6
    • Super System
      NULL
       
  • Scale
    Doc
    LP32888-7
  • Method
    FISH
    LP62864-1

Basic Attributes

Class
MOLPATH.DELDUP
Type
Laboratory
First Released
Version 2.68
Last Updated
Version 2.68 (ADD)
Order vs. Observation
Both

Language Variants Get Info

TagLanguageTranslation
cs-CZCzech (Czechia)Chromozom 1q a 9 a 11 a 15 aneuploidie a 13q delece:Nález:Časový bod:Kostní dřeň:Dokument:Fluorescenční in situ hybridizace (FISH)
el-GRGreek (Greece)Ανευπλοειδία χρωμοσωμάτων 1q & 9 & 11 & 15 & χρωμοσωμική περιοχή 13q διαγραφή:Εύρεση:Pt:Μυελός των οστών:Doc:Φθορίζουσα υβριδοποίηση in situ
Synonyms: Doc MOLPATH MOLPATH.DELDUP Pt Ανευπλοειδία χρωμοσωμάτων 1q & 9 & 11 & 15 & χρωμοσωμική περιοχή 13q διαγραφή Εύρεση Μυελός των οστών Οστό Περιοχή Φθορίζουσα υβριδοποίηση in situ Χρωμόσωμα Χρωμοσωμική περιοχή
es-ESSpanish (Spain)Aneuploidía de cromosoma 1q y 9 y 11 y 15 y región 13q del cromosoma Deleción:Hallazgo:Punto temporal:Médula ósea:Doc:Hibridación in situ fluoresente (FISH)
es-MXSpanish (Mexico)Cromosoma 1q y 9 y 11 y 15 aneuploidía y deleción 13q:Hallazgo:Punto temporal:Médula ósea:Documento:Hibridación fluorescente in situ (FISH)
fr-FRFrench (France)Chromosome 1q et 9 et 11 et 15 aneuploïdie et chromosome région 13q délétion:Recherche:Ponctuel:Moelle osseuse:Document:FISH
it-ITItalian (Italy)Cromosoma 1q & 9 & 11 & 15 aneuploidia & regione cromosomica 13q Delezione:Osservazione:Pt:Mid oss:Doc:FISH
Synonyms: Cromosoma 1q e 9 e 11 e 15 aneuploidia e 13q Delezione o duplicazione genica Ibridazione in situ fluorescente (FISH) Midollo osseo Osservazione Patologia molecolare Punto nel tempo (episodio)
nl-NLDutch (Netherlands)aneuploïdie van chromosoom 1q & 9 & 11 & 15 & chromosomale regio 13q deletie:bevinding:moment:beenmerg:document:FISH
pl-PLPolish (Poland)Aneuploidia chromosomów 1q&9&11&15 & region chromosomowy 13q delecja:stwierdzenie:punkt w czasie:szpik kostny:dokument:FISH
Synonyms: Aneuploidia chromosomów 1q, 9, 11, 15 oraz delecja regionu chromosomowego 13q Aneuploidia chromosomów 1q, 9, 11, 15 oraz region chromosomowy 13q fluorescencyjna hybrydyzacja in situ
zh-CNChinese (China)染色体 1q 与 9 与 11 与 15 非整倍体性 与 染色体区域 13q 缺失:发现:时间点:骨髓:文档型:FISH
Synonyms: Fluorescent in situ hybridization;荧光原位杂交 临床文档型;临床文档;文档;文书;医疗文书;临床医疗文书 分子病理学;分子病理学试验 区;地区;局部 发现是一个原子型临床观察指标，并不是作为印象的概括陈述。体格检查、病史、系统检查及其他此类观察指标的属性均为发现。它们的标尺对于编码型发现可能是名义型，而对于叙述型文本之中所报告的发现，则可能是叙述型。;发现物;所见;结果;结论 时刻;随机;随意;瞬间 染色体 1q 与 9 与 11 与 15 非整倍体性（非整倍体型、非整倍体、异倍体、非整倍性、异倍性、非整倍态、异倍体性） 与 染色体区域（染色体部位、染色体区、染色体区带、染色体部） 13q 染色体二体型+染色体三体型 染色体缺失;染色体区带缺失;基因缺失;缺损;基因缺损;基因删除;删除;基因丢失 染色体部位;染色体区;染色体区带;染色体部;染色体区域（染色体部位、染色体区、染色体区带、染色体部） 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=95069-1