Connectathon 11 Snapshot

This page is part of the FHIR Specification (v1.2.0: STU 3 Draft). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions

1.25.2.1.0 Value Set http://hl7.org/fhir/ValueSet/LOINC-53037-8-answerlist

This is a value set defined by the FHIR project.

Summary

Defining URL:

http://hl7.org/fhir/ValueSet/LOINC-53037-8-answerlist

Name:

LOINC 53037-8 answerlist

Definition:

LOINC answer list for Genetic disease sequence variation interpretation

OID:

2.16.840.1.113883.4.642.2.0 (for OID based terminology systems)

System URL:

http://hl7.org/fhir/LOINC-53037-8-answerlist

System OID:

2.16.840.1.113883.4.642.1.0

Source Resource

XML / JSON

This value set is not currently used

1.25.2.1.0.1 Content Logical Definition

This value set has an inline code system http://hl7.org/fhir/LOINC-53037-8-answerlist, which defines the following codes:

Code	Display	Definition
LA6668-3	Pathogenic	Pathogenic
LA6669-1	Presumed pathogenic	Presumed pathogenic
LA6682-4	Unknown significance	Unknown significance
LA6675-8	Benign	Benign
LA6674-1	Presumed benign	Presumed benign

See the full registry of value sets defined as part of FHIR.

Explanation of the columns that may appear on this page:

Level

A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies

Source

The source of the definition of the code (when the value set draws in codes defined elsewhere)

Code

The code (used as the code in the resource instance)

Display

The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application

Definition

An explanation of the meaning of the concept

Comments

Additional notes about how to use the code