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Term Description

Multigene analysis for both syndromic and non-syndromic forms of hearing loss. Genetic forms of hearing loss may be classified as autosomal dominant, recessive, X-linked or mitochondrial. Determining the cause of hearing loss, whether it is acquired or genetic, is useful for diagnosis, prognosis, and determining treatment options for the patient.[NCBI Books: NBK1434]

LOINC Names Get Info

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

Part Model Get Info

  • Component
    Hearing loss multigene analysis
    LP431382-3
    • Analyte
      Hearing loss multigene analysis
      LP431382-3
      • Component Numerator
        Hearing loss multigene analysis
        LP431382-3
        • Component Numerator Core
          Hearing loss multigene analysis
          LP431382-3
        • 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)Ztráta sluchu multigenová analýza:Nález:Časový bod:Krev/tkáň:Dokument:Molekulární genetika
el-GRGreek (Greece)Πολυγονιδιακή ανάλυση απώλειας ακοής:Εύρεση:Pt:Αίμα/Ιστός:Doc:Μοριακή γενετική
Synonyms: Doc MOLPATH Pt Αίμα Αίμα/Ιστός Απώλεια ακοής Εύρεση Ιστός Μοριακή γενετική Πολυγονιδιακή ανάλυση απώλειας ακοής
es-ESSpanish (Spain)Análisis multigénico de pérdida auditiva:Hallazgo:Punto temporal:Sangre o tejido:Doc:Genética molecular
fr-FRFrench (France)Analyse multigénique d'une perte auditive:Recherche:Ponctuel:Sang/Tissu:Document:Biologie moléculaire
it-ITItalian (Italy)Perdita di udito, analisi multigenica:Osservazione:Pt:Sangue/Tess:Doc:Molgen
Synonyms: Analisi multigenica perdita di udito Genetica molecolare Osservazione Patologia molecolare Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & Strisci
nl-NLDutch (Netherlands)multigen-analyse op gehoorverlies:bevinding:moment:bloed of weefsel:document:moleculair genetisch onderzoek
Synonyms: molgen
pl-PLPolish (Poland)Analiza wielogenowa niedosłuchu:stwierdzenie:punkt w czasie:krew lub tkanka:dokument:genetyka molekularna
Synonyms: Analiza wielogenowa w kierunku niedosłuchu diagnostyka molekularna
zh-CNChinese (China)听力减退多基因分析: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 听力减退（听力损失、听力丧失、失聪）多基因分析 听力损害;听力丧失;听觉损耗 听觉 时刻;随机;随意;瞬间 未作说明的组织;组织;组织 & 涂片 血;血液

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https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=99972-2