47997-2
Genetic variant clinical significance [Interpretation] in Blood or Tissue by Molecular genetics method
Active
Fully-Specified Name
- Component
- Genetic variant clinical significance
- Property
- Imp
- Time
- Pt
- System
- Bld/Tiss
- Scale
- Nom
- Method
- Molgen
Additional Names
- 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
Normative Answer List: LL377-3
Answer | Code | Score | Answer ID |
---|---|---|---|
Pathogenic | LA6668-3 | ||
Presumed Pathogenic | LA6669-1 | ||
Novel Presumed Pathogenic | LA6670-9 | ||
Novel Unknown Significance | LA6671-7 | ||
Novel Presumed Benign | LA6672-5 | ||
Novel | LA6673-3 | ||
Presumed Benign | LA6674-1 | ||
Benign | LA6675-8 | ||
Resistant | LA6676-6 | ||
Responsive | LA6677-4 | ||
Novel Presumed Non-Responsive | LA6678-2 | ||
Novel Presumed Responsive | LA6679-0 | ||
Unclassified | LA6680-8 | ||
Polymorphism | LA6681-6 | ||
Unknown Significance | LA6682-4 |
Basic Attributes
- Class
- MOLPATH.MISC
- Type
- Laboratory
- First Released
- Version 2.21
- Last Updated
- Version 2.73
- Order vs. Observation
- Observation
- Common Test Rank Get Info
- 18483
Member of these Panels
LOINC | Long Common Name |
---|---|
48014-5 | Sequence variation panel - Blood or Tissue by Molecular genetics method |
Language Variants Get Info
Tag | Language | Translation |
---|---|---|
es-ES | Spanish (Spain) | Significado clínico de variante genética: |
es-MX | Spanish (Mexico) | Importancia clínica de la variante genética: |
fr-FR | French (France) | Variant génétique signification clinique: |
it-IT | Italian (Italy) | Variante genetica, significato clinico: 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 & |
nl-NL | Dutch (Netherlands) | genetische variant klinische significantie: Synonyms: molgen |
pt-BR | Portuguese (Brazil) | Significado da variação genética clínica: Synonyms: ; |
ru-RU | Russian (Russian Federation) | Генетический вариант клиническая значимость: Synonyms: Впечатление/интерпретация исследования Кровь Кровь или Ткань Номинальный; |
tr-TR | Turkish (Turkey) | Genetik varyant klinik anlamlılık: |
zh-CN | Chinese (China) | 遗传变异临床意义: Synonyms: 全血或组织; |
LOINC Terminology Service (API) using HL7® FHIR® Get Info
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- CodeSystem lookup
- https:
//fhir.loinc.org/CodeSystem/$lookup?system=http: //loinc.org&code=47997-2
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