Onconova Implementation Guide
0.2.0 - ci-build
Onconova Implementation Guide - Local Development build (v0.2.0) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions
| Official URL: http://onconova.github.io/fhir/ValueSet/onconova-vs-dna-change-types | Version: 0.2.0 | |||
| Active as of 2026-03-18 | Computable Name: DNAChangeTypes | |||
Coding DNA change types due to a genomic variant. It constraints and expands the original LOINC Answer List LL380-7 to enforce Onconova-compatible codes
References
This value set includes codes based on the following rules:
http://sequenceontology.org version Not Stated (use latest from terminology server)| Code | Display |
| SO:1000002 | substitution |
| SO:1000032 | delins |
| SO:0000667 | insertion |
| SO:0000159 | deletion |
| SO:1000035 | duplication |
| SO:1000036 | inversion |
| SO:0002073 | no_sequence_alteration |
| SO:0002096 | short_tandem_repeat_variation |
| SO:0000199 | translocation |
| SO:0000453 | transposition |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl version Not Stated (use latest from terminology server)
| Code | Display |
| C17961 | DNA Methylation |
No Expansion for this valueset (Unknown Code System)
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 |
| System | 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 |