Prescription Search Support, published by HL7 Belgium. This guide is not an authorized publication; it is the continuous build for version 1.0.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/hl7-be/pss/ and changes regularly. See the Directory of published versions
Generated Narrative: QuestionnaireResponse antimicroguidance-request
LinkID | Text | Definition | Answer |
---|---|---|---|
![]() ![]() | Questionnaire:None specified | ||
![]() ![]() ![]() | |||
![]() ![]() ![]() ![]() | Indication | SNOMED CT (all versions) 921000172108: Acute keelpijn (version = http://snomed.info/sct/11000172109 ) | |
![]() ![]() ![]() ![]() | false | ||
![]() ![]() ![]() ![]() | true | ||
![]() ![]() ![]() ![]() | |||
![]() ![]() ![]() ![]() ![]() | false | ||
![]() ![]() ![]() ![]() ![]() | |||
![]() ![]() ![]() ![]() ![]() ![]() | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() | true | ||
![]() ![]() ![]() ![]() ![]() ![]() | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() | SNOMED CT (all versions) 763597000: Hereditary ataxia (disorder) (version = http://snomed.info/sct/11000172109 ) | ||
![]() ![]() ![]() ![]() ![]() ![]() ![]() | false | ||
![]() ![]() ![]() ![]() ![]() ![]() | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() | false | ||
![]() ![]() ![]() ![]() ![]() ![]() | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() | false | ||
![]() ![]() ![]() ![]() ![]() ![]() | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() | false | ||
![]() ![]() ![]() ![]() | false | ||
![]() ![]() ![]() ![]() | false | ||