| Package | nictiz.fhir.nl.stu3.geboortezorg |
| Type | ValueSet |
| Id | 2.16.840.1.113883.2.4.11.198--20161026164418 |
| FHIR Version | R3 |
| Source | https://simplifier.net/resolve?scope=nictiz.fhir.nl.stu3.geboortezorg@1.3.3-rc7&canonical=http://decor.nictiz.nl/fhir/ValueSet/2.16.840.1.113883.2.4.11.198--20161026164418 |
| URL | http://decor.nictiz.nl/fhir/ValueSet/2.16.840.1.113883.2.4.11.198--20161026164418 |
| Version | 2.3.0 |
| Status | active |
| Name | ChromosomaleAfwijkingen22 |
| Title | ChromosomaleAfwijkingen |
| Realm | nl |
| Description | ChromosomaleAfwijkingen |
| Copyright | This artefact includes content from SNOMED Clinical Terms® (SNOMED CT®) which is copyright of the International Health Terminology Standards Development Organisation (IHTSDO). Implementers of these artefacts must have the appropriate SNOMED CT Affiliate license - for more information contact http://www.snomed.org/snomed-ct/getsnomed-ct or info@snomed.org. <div data-source="inherited" style="border-top: 1px solid black">This artefact includes content from SNOMED Clinical Terms® (SNOMED CT®) which is copyright of the International Health Terminology Standards Development Organisation (IHTSDO). Implementers of these artefacts must have the appropriate SNOMED CT Affiliate license - for more information contact http://www.snomed.org/snomed-ct/getsnomed-ct or info@snomed.org.</div> |
No resources found
| CodeSystem | |
| sct | SNOMED CT (all versions) |
| sct | SNOMED codes used in this IG |
| sct | veri |
No narrative content found in resource
FHIR