81259-4
Associated phenotype
Trial
Status Information
- Status
- TRIAL
Term Description
The possible phenotype associated with the genetic variant found in this study.
Source: Regenstrief LOINC
Fully-Specified Name
- Component
- Associated phenotype
- Property
- Find
- Time
- Pt
- System
- ^Patient
- Scale
- Nom
- Method
Additional Names
- Short Name
- Prob assoc phenotype
- Display Name
- Associated phenotype
- Consumer Name Alpha Get Info
- Associated phenotype
Basic Attributes
- Class
- MOLPATH
- Type
- Laboratory
- First Released
- Version 2.56
- Last Updated
- Version 2.71
- Order vs. Observation
- Observation
Member of these Panels
LOINC | Long Common Name |
---|---|
81247-9 | Master HL7 genetic variant reporting panel |
Language Variants Get Info
Tag | Language | Translation |
---|---|---|
es-ES | Spanish (Spain) | Fenotipo asociado probable: |
es-MX | Spanish (Mexico) | Fenotipo asociado: |
fr-FR | French (France) | Phénotype associé: |
it-IT | Italian (Italy) | Probabile fenotipo associato: Synonyms: Osservazione Patologia molecolare paziente Punto nel tempo (episodio) |
zh-CN | Chinese (China) | 关联表型: Synonyms: 关联(相关、 |
LOINC Terminology Service (API) using HL7® FHIR® Get Info
Requests to this service require a free LOINC username and password. Below is a sample of the possible capabilities. See the LOINC Terminology Service documentation for more information.
- CodeSystem lookup
- https:
//fhir.loinc.org/CodeSystem/$lookup?system=http: //loinc.org&code=81259-4
LOINC Copyright
Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright