FHIR Cross-Version Extensions package for FHIR R4 from FHIR R4B - Version 0.0.1-snapshot-2. See the Directory of published versions
| Official URL: http://hl7.org/fhir/4.3/ValueSet/R4B-sequence-referenceSeq-for-R4 | Version: 0.0.1-snapshot-2 | |||
| Standards status: Informative | Maturity Level: 1 | Responsible: Clinical Genomics | Computable Name: R4B_sequence_referenceSeq_for_R4 | |
| This cross-version ValueSet represents concepts from http://hl7.org/fhir/ValueSet/sequence-referenceSeq | 4.3.0 for use in FHIR R4. Concepts not present here have direct equivalent mappings crossing all versions from R4B to R4. |
References
This value set is not used here; it may be used elsewhere (e.g. specifications and/or implementations that use this content)
This value set includes codes based on the following rules:
http://www.ensembl.orghttp://www.ncbi.nlm.nih.gov/nuccore
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 |