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Part Descriptions

LP36171-4   1p & 19q chromosome
Diagnostic and prognostic marker for oligodendroglioma. Patients with 1p and 19q deletions have a better prognosis than those patients that do not have 1p and 19q deletions. Source: Regenstrief Institute

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
1p & 19q chromosome deletion:Find:Pt:Tiss:Doc:FISH
Long Common Name
1p and 19q chromosome deletion in Tissue by FISH
Short Name
1p+19q Del Tiss FISH
Display Name
1p and 19q chromosome del FISH Doc (Tiss)
Consumer Name Alpha Get Info
1p and 19q chromosome deletion analysis, Tissue

Part Model Get Info

  • Component
    1p & 19q chromosome deletion
    LP227502-4
    • Analyte
      1p & 19q chromosome deletion
      LP227502-4
      • Component Numerator
        1p & 19q chromosome deletion
        LP227502-4
        • Component Numerator Core
          1p & 19q chromosome
          LP36171-4
        • 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
    Tiss
    LP7641-6
    • System Core
      Tiss
      LP7641-6
    • Super System
      NULL
       
  • Scale
    Doc
    LP32888-7
  • Method
    FISH
    LP62864-1

Basic Attributes

Class
MOLPATH.DELDUP
Type
Laboratory
First Released
Version 2.79
Last Updated
Version 2.79 (ADD)
Order vs. Observation
Both

Language Variants Get Info

TagLanguageTranslation
el-GRGreek (Greece)Χρωμόσωμα 1p & 19q διαγραφή:Εύρεση:Pt:Ιστός:Doc:Φθορίζουσα υβριδοποίηση in situ
Synonyms: Doc MOLPATH MOLPATH.DELDUP Pt διαγραφή Εύρεση Ιστός Φθορίζουσα υβριδοποίηση in situ Χρωμόσωμα Χρωμόσωμα 19q Χρωμόσωμα 1p & 19q
es-ESSpanish (Spain)Gen Del(1p,19q) Deleción:Hallazgo:Punto temporal:Tejido:Doc:Hibridación in situ fluoresente (FISH)
fr-FRFrench (France)Chromosome 1p et 19q délétion:Recherche:Ponctuel:Tissu:Document:FISH
it-ITItalian (Italy)1p & 19q, cromosoma Delezione:Osservazione:Pt:Tessuto:Doc:FISH
Synonyms: Cromosoma 19q Cromosoma 1p & 19q Delezione o duplicazione genica Ibridazione in situ fluorescente (FISH) Osservazione Patologia molecolare Punto nel tempo (episodio) Tessuto & Strisci
nl-NLDutch (Netherlands)1p- & 19q-chromosoom deletie:bevinding:moment:weefsel en uitstrijkjes:document:FISH
pl-PLPolish (Poland)Chromosom 1p & 19q delecja:stwierdzenie:punkt w czasie:tkanka i rozmazy:dokument:FISH
Synonyms: Chromosom 1p i 19q Delecja długiego ramienia chromosomu 19 fluorescencyjna hybrydyzacja in situ Kodelecja ramion chromosomów 1p&19q; delecja ramienia krótkiego chromosomu 1 i ramienia długiego chromosomu 19 Ramię długie chromosomu 19
tr-TRTurkish (Turkey)1p ve 19q kromozom delesyon:Bulgu:Zmlı:Doku:Dokm:FISH
zh-CNChinese (China)Del(1p,19q) 基因 缺失:发现:时间点:组织与涂片:文档型:FISH
Synonyms: 19q 染色体 1p & 19q;1p/19q;d(1p,19q);del(1p,19q);寡枝神经胶质细胞瘤;寡树突胶质瘤;少枝胶质瘤;少枝胶质细胞瘤;少突胶质细胞瘤 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 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 未作说明的组织;组织;组织 & 涂片 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

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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=107239-6