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LOINC Names Get Info

Fully-Specified Name
Genetic variant clinical significance:Imp:Pt:Bld/Tiss:Nom:Molgen
Long Common Name
Genetic variant clinical significance [Interpretation] in Blood or Tissue by Molecular genetics method
Short Name
Genetic variant clin sig Bld/T-Imp
Display Name
Genetic variant clinical significance Molgen (Bld/Tiss) [Interp]
Consumer Name Alpha Get Info
Genetic variant clinical significance, Blood or tissue specimen

Part Model Get Info

  • Component
    Genetic variant clinical significance
    LP62054-9
    • Analyte
      Genetic variant clinical significance
      LP62054-9
      • Component Numerator
        Genetic variant clinical significance
        LP62054-9
        • Component Numerator Core
          Genetic variant clinical significance
          LP62054-9
        • 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/Tiss
    LP7061-7
    • System Core
      Bld/Tiss
      LP7061-7
    • Super System
      NULL
       
  • Scale
    Nom
    LP7750-5
  • Method
    Molgen
    LP6404-0

Normative Answer List: LL377-3

AnswerCodeScoreAnswer ID
PathogenicLA6668-3
Presumed PathogenicLA6669-1
Novel Presumed PathogenicLA6670-9
Novel Unknown SignificanceLA6671-7
Novel Presumed BenignLA6672-5
NovelLA6673-3
Presumed BenignLA6674-1
BenignLA6675-8
ResistantLA6676-6
ResponsiveLA6677-4
Novel Presumed Non-ResponsiveLA6678-2
Novel Presumed ResponsiveLA6679-0
UnclassifiedLA6680-8
PolymorphismLA6681-6
Unknown SignificanceLA6682-4

Basic Attributes

Class
MOLPATH.MISC
Type
Laboratory
First Released
Version 2.21
Last Updated
Version 2.73 (MIN)
Order vs. Observation
Observation
Common Test Rank Get Info
18483

Member of these Panels

LOINCLong Common Name
48014-5Sequence variation panel - Blood or Tissue by Molecular genetics method

Language Variants Get Info

TagLanguageTranslation
cs-CZCzech (Czechia)Genetická varianta klinický význam:Interpretace:Časový bod:Krev/tkáň:Nominální:Molekulární genetika
el-GRGreek (Greece)Κλινική σημασία γενετικής παραλλαγής:Imp:Pt:Αίμα/Ιστός:Nom:Μοριακή γενετική
Synonyms: Imp MISC MOLPATH MOLPATH.MISC Nom Pt Αίμα Αίμα/Ιστός Ιστός Κλινική σημασία γενετικής παραλλαγής Μοριακή γενετική
es-ESSpanish (Spain)Significado clínico de variante genética:Impresión/interpretación del estudio:Punto temporal:Sangre o tejido:Nom:Genética molecular
es-MXSpanish (Mexico)Importancia clínica de la variante genética:Impresión / interpretación del estudio:Punto temporal:Sangre o tejido:Nominal:Genética molecular
fr-FRFrench (France)Variant génétique signification clinique:Interprétation:Ponctuel:Sang/Tissu:Résultat nominal:Biologie moléculaire
it-ITItalian (Italy)Variante genetica, significato clinico:Imp:Pt:Sangue/Tess:Nom:Molgen
Synonyms: Genetica molecolare Impressione/interpretazione di studio Miscellanea Miscellanea geni Patologia molecolare Punto nel tempo (episodio) Sangue Sangue o Tessuto Significato clinico di variante genetica Tessuto & Strisci
nl-NLDutch (Netherlands)genetische variant klinische significantie:interpretatie:moment:bloed of weefsel:nominaal:moleculair genetisch onderzoek
Synonyms: molgen
pl-PLPolish (Poland)Wariant geneteczny klinicznie istotny:ocena:punkt w czasie:krew lub tkanka:skala nominalna:genetyka molekularna
Synonyms: diagnostyka molekularna Wariant genteczny o klinicznej istotności wynik kategorialny
pt-BRPortuguese (Brazil)Significado da variação genética clínica:Imp:Pt:Sg/Tecido:Nom:Genética molecular
Synonyms: ; Genetic variant clin sig; Variant Interpretation; Interp; Impression; Impressions; Point in time; Random; Bld/T; Tissue; Bld/T; Blood; WB; Whole blood; Nominal; PCR; Molecular genetics; Molecular pathology
ru-RURussian (Russian Federation)Генетический вариант клиническая значимость:Впчт:ТчкВрм:Кр/Тк:Ном:МолГен
Synonyms: Впечатление/интерпретация исследования Кровь Кровь или Ткань Номинальный;Именной Ткань и мазки Точка во времени;Момент
tr-TRTurkish (Turkey)Genetik varyant klinik anlamlılık:İzlnm:Zmlı:Kan/Dk:Snf:Molgen
zh-CNChinese (China)遗传变异临床意义:印象:时间点:全血/组织:名义型:分子遗传学类实验室方法
Synonyms: 全血或组织;血液/组织;血液或组织 分子病理学.杂项;分子病理学试验.杂项;分子病理学试验类.其他 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 分类型应答;分类型结果;名义性;名称型;名词型;名词性;标称性;没有自然次序的名义型或分类型应答 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 未作说明的组织;组织;组织 & 涂片 杂项;杂项类;杂项试验 血;血液 遗传变异（遗传性变异、基因变异、传性变型、遗传变异体、基因变异体）临床意义;变型解释;遗传性变型临床意义;遗传变异临床意义;遗传变异体临床意义

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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=47997-2