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Term Description

Multigene testing for heritable germline mutations in genes associated with cancer in various organ systems, including breast and gynecologic (breast, ovarian, uterine), gastrointestinal (colorectal, gastric, pancreatic), endocrine (thyroid, paraganglioma/pheochromocytoma, parathyroid, pituitary), genitourinary (renal/urinary tract, prostate), skin (melanoma, basal cell carcinoma), brain/nervous system, and bone/soft tissue (sarcoma) & blood (myelodysplastic syndrome/leukemia). Testing is performed to confirm a diagnosis and help guide treatment and management decisions. Identification of a disease-causing variants may also used to inform at-risk relatives. Approximately 5-10 percent of cancers are thought to be hereditary. PMID: 15637391 This test is not appropriate for the detection of somatic mutations in tumor tissue since it is focused on heritable germline mutations.

LOINC Names Get Info

Fully-Specified Name
Hereditary cancer multigene analysis:Find:Pt:Bld/Tiss:Doc:Molgen
Long Common Name
Hereditary cancer multigene analysis in Blood or Tissue by Molecular genetics method
Short Name
Hereditary Cancer Multigene Anl Bld/T
Display Name
Hereditary cancer multigene analysis Molgen Doc (Bld/Tiss)
Consumer Name Alpha Get Info
Hereditary cancer multigene analysis, Blood or tissue specimen

Part Model Get Info

  • Component
    Hereditary cancer multigene analysis
    LP426461-2
    • Analyte
      Hereditary cancer multigene analysis
      LP426461-2
      • Component Numerator
        Hereditary cancer multigene analysis
        LP426461-2
        • Component Numerator Core
          Hereditary cancer multigene analysis
          LP426461-2
        • Component Numerator Core Suffix
          NULL
           
      • 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
    Bld/Tiss
    LP7061-7
    • System Core
      Bld/Tiss
      LP7061-7
    • Super System
      NULL
       
  • Scale
    Doc
    LP32888-7
  • Method
    Molgen
    LP6404-0

Basic Attributes

Class
MOLPATH
Type
Laboratory
First Released
Version 2.70
Last Updated
Version 2.70 (ADD)
Order vs. Observation
Both

Language Variants Get Info

TagLanguageTranslation
cs-CZCzech (Czechia)Hereditární karcinom multigenová analýza:Nález:Časový bod:Krev/tkáň:Dokument:Molekulární genetika
el-GRGreek (Greece)Πολυγονιδιακή ανάλυση κληρονομικού καρκίνου:Εύρεση:Pt:Αίμα/Ιστός:Doc:Μοριακή γενετική
Synonyms: Doc MOLPATH Pt Αίμα Αίμα/Ιστός Εύρεση Ιστός Καρκίνος Μοριακή γενετική Πολυγονιδιακή ανάλυση κληρονομικού καρκίνου
es-ESSpanish (Spain)Análisis multigénico de cáncer hereditario:Hallazgo:Punto temporal:Sangre o tejido:Doc:Genética molecular
es-MXSpanish (Mexico)Análisis multigénico de cáncer hereditario:Encontrar:Punto temporal:Bld / Tiss:Documento:Molgen
fr-FRFrench (France)Analyse multigénique d'un cancer héréditaire:Recherche:Ponctuel:Sang/Tissu:Document:Biologie moléculaire
it-ITItalian (Italy)Cancro ereditario, analisi multigenica:Osservazione:Pt:Sangue/Tess:Doc:Molgen
Synonyms: Analisi multigenica del cancro ereditario Genetica molecolare Osservazione Patologia molecolare Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & Strisci
nl-NLDutch (Netherlands)erfelijke kanker multigen-analyse:bevinding:moment:bloed of weefsel:document:moleculair genetisch onderzoek
Synonyms: molgen
pl-PLPolish (Poland)Analiza wielogenowa nowotworów dziedzicznych:stwierdzenie:punkt w czasie:krew lub tkanka:dokument:genetyka molekularna
Synonyms: Analiza wielogenowa w kierunku nowotworów dziedzicznych diagnostyka molekularna
zh-CNChinese (China)遗传性癌症多基因分析:发现:时间点:全血/组织:文档型:分子遗传学类实验室方法
Synonyms: 临床文档型;临床文档;文档;文书;医疗文书;临床医疗文书 全血或组织;血液/组织;血液或组织 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 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 癌 血;血液 遗传性癌症（遗传性癌）多基因分析

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