51968-6
Discrete variation analysis overall interpretation
Active
Term Description
Interpretation of all identified DNA Markers and/or Individual Alleles along with any known clinical information for the benefit of aiding clinicians in understanding the results overall. This is used for Symptomatic or Asymptomatic testing other than Carrier testing.
LOINC Names Get Info
- Fully-Specified Name
- Genetic disease analysis overall interpretation:
Imp: Pt: Bld/Tiss: Nom: Molgen - Long Common Name
- Discrete variation analysis overall interpretation
- Short Name
- Gene dis anl interp-Imp
- Display Name
- Genetic disease analysis overall interpretation Molgen (Bld/Tiss) [Interp]
- Consumer Name Alpha Get Info
- Genetic disease analysis overall interpretation, Blood or tissue specimen
Part Model Get Info
- Component
- Genetic disease analysis overall interpretation
LP66901-7
- Analyte
- Genetic disease analysis overall interpretation
LP66901-7
- Challenge
- NULL
- Adjustment
- NULL
- Count
- NULL
- Property
- Imp
LP6819-9
- Time
- Pt
LP6960-1
- Time Core
- Pt
LP6960-1
- Time Modifier
- NULL
- System
- Bld/Tiss
LP7061-7
- System Core
- Bld/Tiss
LP7061-7
- Super System
- NULL
- Scale
- Nom
LP7750-5
- Method
- Molgen
LP6404-0
Preferred Answer List: LL541-4
Source: Regenstrief LOINC| Answer | Code | Score | Answer ID |
|---|---|---|---|
| PositiveCopyright http://snomed.info/sct ID:10828004 Positive (qualifier value) | LA6576-8 | ||
| NegativeCopyright http://snomed.info/sct ID:260385009 Negative (qualifier value) | LA6577-6 | ||
| InconclusiveCopyright http://snomed.info/sct ID:419984006 Inconclusive (qualifier value) | LA9663-1 | ||
| Failure | LA9664-9 |
Basic Attributes
- Class
- HL7.GENETICS
- Type
- Laboratory
- First Released
- Version 2.24
- Last Updated
- Version 2.73 (MIN)
- Change Reason
- Updated LCN per CJM for HL7 CG IG
- Order vs. Observation
- Observation
- Common Test Rank Get Info
- 8725
Member of these Panels
| LOINC | Long Common Name |
|---|---|
| 55233-1 | Genetic analysis master panel |
| 51966-0 | Genetic disease DNA analysis panel |
| 81247-9 | Master HL7 genetic variant reporting panel |
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| cs-CZ | Czech (Czechia) | Genetické onemocnění analýza celková interpretace: |
| de-AT | German (Austria) | Synonyms: Befundinterpretation Humangenetik |
| el-GR | Greek (Greece) | Γενική ερμηνεία ανάλυσης γενετικής νόσου: Synonyms: HL7.GENETICS Imp Nom Pt Αίμα Αίμα/Ιστός Γενική ερμηνεία ανάλυσης γενετικής νόσου Γενική ερμηνεία ανάλυσης νόσου Ερμηνεία Ιστός Μοριακή γενετική |
| es-ES | Spanish (Spain) | Interpretación general del análisis en la enfermedad genética: |
| es-MX | Spanish (Mexico) | Interpretación general del análisis de enfermedades genéticas: |
| fr-FR | French (France) | Maladie génétique interprétation globale: |
| it-IT | Italian (Italy) | Malattia genetica, interpretazione generale analisi: Synonyms: Genetica molecolare Impressione/interpretazione di studio Interpretazione generale di analisi di malattia ge Punto nel tempo (episodio) Referto clinico di test genetico Sangue Sangue o Tessuto Tessuto & |
| pl-PL | Polish (Poland) | Ogólna interpretacja analizy chorób genetycznych: Synonyms: diagnostyka molekularna wynik kategorialny |
| pt-BR | Portuguese (Brazil) | Doenças genéticas análise total interpretação: Synonyms: Interp; |
| ru-RU | Russian (Russian Federation) | Генетические заболевания анализ общая интерпретация: Synonyms: Впечатление/интерпретация исследования Кровь Кровь или Ткань Номинальный; |
| tr-TR | Turkish (Turkey) | Genetik hastalık analizi tüm yorumu: |
| zh-CN | Chinese (China) | 遗传性疾病分析总体解释: Synonyms: HL7 遗传学 全血或组织; |
LOINC Terminology Service (API) using HL7® FHIR® Get Info
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Third Party Copyright
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LOINC Copyright
Copyright © Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://