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Term Description

Multigene testing for atypical hemolytic uremic syndrome (aHUS), a condition that can begin in the neonatal period to adulthood and consists of hemolytic anemia, thrombocytopenia, and renal failure caused by platelet thrombi in the kidney and other organs. Genes associated with genetic aHUS include C3, C5, CD46, CFB, CFH, CFHR1, CFHR2, CFHR3, CFHR4, CFHR5, CFI, DGKE, PLG, THBD, and MMACHC. Testing is performed for diagnostic, prognostic, and therapeutic assessment in patients with aHUS.[NCBI Books: NBK1367]

LOINC Names Get Info

Fully-Specified Name
Atypical hemolytic uremic syndrome multigene analysis:Find:Pt:Bld/Tiss:Doc:Molgen
Long Common Name
Atypical hemolytic uremic syndrome multigene analysis in Blood or Tissue by Molecular genetics method
Short Name
aHUS multigene analysis Bld/T
Display Name
Atypical hemolytic uremic syndrome multigene analysis Molgen Doc (Bld/Tiss)
Consumer Name Alpha Get Info
Atypical hemolytic uremic syndrome multigene analysis, Blood or tissue specimen

Part Model Get Info

  • Component
    Atypical hemolytic uremic syndrome multigene analysis
    LP431375-7
    • Analyte
      Atypical hemolytic uremic syndrome multigene analysis
      LP431375-7
      • Component Numerator
        Atypical hemolytic uremic syndrome multigene analysis
        LP431375-7
        • Component Numerator Core
          Atypical hemolytic uremic syndrome multigene analysis
          LP431375-7
        • 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 2.72
Last Updated
Version 2.72 (ADD)
Order vs. Observation
Both

Language Variants Get Info

TagLanguageTranslation
cs-CZCzech (Czechia)Hemolyticko-uremický syndrom atypický multigenová analýza:Nález:Časový bod:Krev/tkáň:Dokument:Molekulární genetika
el-GRGreek (Greece)Πολυγονιδιακή ανάλυση του άτυπου αιμολυτικού ουραιμικού συνδρόμου:Εύρεση:Pt:Αίμα/Ιστός:Doc:Μοριακή γενετική
Synonyms: Doc MOLPATH Pt Αίμα Αίμα/Ιστός Εύρεση Ιστός Μοριακή γενετική Πολυγονιδιακή ανάλυση του άτυπου αιμολυτικού ουραιμικού συνδρόμου
es-ESSpanish (Spain)Análisis multigénico del síndrome urémico hemolítico atípico:Hallazgo:Punto temporal:Sangre o tejido:Doc:Genética molecular
fr-FRFrench (France)Analyse multigénique d'un syndrome hémolytique urémique atypique:Recherche:Ponctuel:Sang/Tissu:Document:Biologie moléculaire
it-ITItalian (Italy)Analisi multigenica della sindrome emolitico uremica atipica:Osservazione:Pt:Sangue/Tess:Doc:Molgen
Synonyms: Genetica molecolare Osservazione Patologia molecolare Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & Strisci
nl-NLDutch (Netherlands)multigen-analyse op atypisch hemolytisch-uremisch syndroom:bevinding:moment:bloed of weefsel:document:moleculair genetisch onderzoek
Synonyms: aHUS; atypish HUS; niet diarree-geassocieerd hemolytisch-uremisch syndroom molgen
pl-PLPolish (Poland)Analiza wielogenowa nietypowego zespołu hemolityczno-mocznicowego:stwierdzenie:punkt w czasie:krew lub tkanka:dokument:genetyka molekularna
Synonyms: Analiza wielogenowa w kierunku aHUS diagnostyka molekularna
zh-CNChinese (China)非典型溶血性尿毒综合征多基因分析:发现:时间点:全血/组织:文档型:分子遗传学类实验室方法
Synonyms: 不典型 不典型的 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 反应性 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 血;血液 非典型 非典型溶血性尿毒综合征（aHUS、非典型性溶血性尿毒综合征、非典型溶血尿毒综合征、非典型溶血性尿毒症综合征、非典型溶血尿毒症综合征）多基因分析 非典型的

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