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Status Information

Status
DISCOURAGED
Comment
We discourage the use of this term (though it is allowed) because it combines independent tests for independent disorders. We recommend reporting the interpretation of screening results for biotinidase deficiency, cystic fibrosis and right/left ear hearing loss separately using 46761-3, 46769-6, 54109-4 and 54108-6, respectively.
Map-ToLong Common NameMapping Guidance
46761-3Biotinidase deficiency newborn screen interpretation
46769-6Cystic fibrosis newborn screen interpretation
54108-6Newborn hearing screen of Ear - left
54109-4Newborn hearing screen of Ear - right

LOINC Names Get Info

Fully-Specified Name
Genetic disorders:Imp:Pt:Bld.dot:Ord:
Long Common Name
Genetic.Disorders newborn screen interpretation
Short Name
Genetic.Disorders DBS-Imp
Display Name
Genetic.Disorders Ql (DBS) [Interp]
Consumer Name Alpha Get Info
Genetic.Disorders, Dried blood spot

Part Model Get Info

  • Component
    Genetic disorders
    LP56740-1
    • Analyte
      Genetic disorders
      LP56740-1
      • Component Numerator
        Genetic disorders
        LP56740-1
        • Component Numerator Core
          Genetic disorders
          LP56740-1
        • Component Numerator Core Suffix
          NULL
           
      • Component Denominator
        NULL
         
        • Component Denominator Core
          NULL
           
        • Component Denominator Core Suffix
          NULL
           
    • Challenge
      NULL
       
    • Adjustment
      NULL
       
    • Count
      NULL
       
  • Property
    Imp
    LP6819-9
  • Time
    Pt
    LP6960-1
  • System
    Bld.dot
    LP21304-8
    • System Core
      Bld.dot
      LP21304-8
    • Super System
      NULL
       
  • Scale
    Ord
    LP7751-3
  • Method
    NULL
     

Basic Attributes

Class
CHEM
Type
Laboratory
First Released
Version 2.19
Last Updated
Version 2.73 (MIN)
Order vs. Observation
Observation
Common Test Rank Get Info
9307

Language Variants Get Info

TagLanguageTranslation
cs-CZCzech (Czechia)Genetické.poruchy:Interpretace:Časový bod:Suchá krevní kapka (DBS):Ordinální:
el-GRGreek (Greece)Γενετικές διαταραχές:Imp:Pt:Bld.dot:Ord:
Synonyms: Bld.dot CHEM Imp Ord Pt Αίμα Γενετικές διαταραχές
es-ESSpanish (Spain)Trastornos genéticos:Impresión/interpretación del estudio:Punto temporal:gota de sangre (papel de filtro):Ord:
es-MXSpanish (Mexico)Desordenes genéticos:Impresión / interpretación del estudio:Punto temporal:DBS:Ordinal:
fr-CAFrench (Canada)Troubles génétiques:Impression:Temps ponctuel:Sang sur papier filtre:Ordinal:
fr-BEFrench (Belgium)Troubles génétiques:Impression/interprétation d'étude:Temps ponctuel:Sang sur papier filtre:Ordinal:
Synonyms: Maladies génétiques
it-ITItalian (Italy)Disturbi genetici:Imp:Pt:Sangue.su carta da filtro:Ord:
Synonyms: Chimica Disturbi.Genetici Impressione/interpretazione di studio Punto nel tempo (episodio) Sangue Spot sangue secco
nl-NLDutch (Netherlands)genetische aandoeningen:interpretatie:moment:gedroogde bloedspot:ordinaal:
pl-PLPolish (Poland)Zaburzenia genetyczne:ocena:punkt w czasie:sucha kropla krwi:uporządkowany:
pt-BRPortuguese (Brazil)Doenças genéticas:Imp:Pt:SgPapel:Ord:
Synonyms: Interpretation; Interp; Impression; Impressions; Point in time; Random; DBS; Filter paper; FP; Dried blood spot; Blood; WB; Whole blood; Ql; Ordinal; QL; Qualitative; Qual; Screen; Chemistry
tr-TRTurkish (Turkey)Genetik bozukluklar:İzlnm:Zmlı:Kan.nokta:Srl:
zh-CNChinese (China)遗传性疾病:印象:时间点:全血.斑点:序数型:
Synonyms: 依次型;分类顺序型;定性的;序数型（或称等级型）;性质上的;有序型;有序性分类应答;有序性分类结果;秩次型;等级型;筛查;顺序型 全血斑点(滤纸);滤纸;血液.斑点;血液斑点(滤纸) 化学;化学检验项目;化学检验项目类;化学类;化学试验;非刺激耐受型化学检验项目;非刺激耐受型化学检验项目类;非刺激耐受型化学试验;非刺激耐受型化学试验类 印象是一种诊断陈述，始终是对其他某种观察指标的解释或抽象（一系列检验项目结果、一幅图像或者整个某位病人），而且几乎总是由某位专业人员产生。;检查印象;检查印象/解释;检查的印象/解释;检查解释;解释;阐释 时刻;随机;随意;瞬间 血;血液 遗传性.疾病;遗传性.障碍;遗传性疾病类;遗传性障碍;遗传性障碍类;遗传病

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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=46738-1