Mappings for the Profile.
Genomics Report |
DiagnosticReport | |
extension | |
extension (related-artifact) | |
extension (recommended-action) | N/A (from other CG FHIR work) |
valueReference | N/A (from other CG FHIR work) |
extension (supportingInfo) | N/A (from other CG FHIR work) |
valueReference | N/A (from other CG FHIR work) |
result (obs-gen-panel) | TBD |
result (overall) | A.8 |
result (deletion-dup) | A.9 |
result (inh-dis-path) | TBD |
result (som-diagnostic) | TBD |
result (som-prognostic) | TBD |
result (som-predictive) | TBD |
result (med-metabolism) | TDB |
result (med-efficacy) | TDB |
result (med-high-risk) | TDB |
result (obs-cytogenetic-nomenclature) | TBD |
result (obs-genotype) | TBD |
result (obs-haplotype) | TBD |
result (obs-complex-variant) | TBD |
result (obs-described-variant) | TBD |
result (obs-region-studied) | TBD |
presentedForm | A.10 |
Genomics Report |
DiagnosticReport | ORU -> OBR |
identifier | OBR-51/ for globally unique filler ID - OBR-3 , For non-globally unique filler-id the flller/placer number must be combined with the universal service Id - OBR-2(if present)+OBR-3+OBR-4 |
basedOn | ORC? OBR-2/3? |
status | OBR-25 (not 1:1 mapping) |
category | OBR-24 |
code | OBR-4 (HL7 v2 doesn't provide an easy way to indicate both the ordered test and the performed panel) |
coding | C*E.1-8, C*E.10-22 |
coding (code) | C*E.1-8, C*E.10-22 |
system | C*E.3 |
version | C*E.7 |
code | C*E.1 |
display | C*E.2 - but note this is not well followed |
userSelected | Sometimes implied by being first |
text | C*E.9. But note many systems use C*E.2 for this |
subject | PID-3 (no HL7 v2 mapping for Group or Device) |
encounter | PV1-19 |
effective[x] | OBR-7 |
issued | OBR-22 |
performer | PRT-8 (where this PRT-4-Participation = "PO") |
resultsInterpreter | OBR-32, PRT-8 (where this PRT-4-Participation = "PI") |
specimen | SPM |
result | OBXs |
result (obs-gen-panel) | OBXs |
result (overall) | OBXs |
result (deletion-dup) | OBXs |
result (inh-dis-path) | OBXs |
result (som-diagnostic) | OBXs |
result (som-prognostic) | OBXs |
result (som-predictive) | OBXs |
result (med-metabolism) | OBXs |
result (med-efficacy) | OBXs |
result (med-high-risk) | OBXs |
result (obs-cytogenetic-nomenclature) | OBXs |
result (obs-genotype) | OBXs |
result (obs-haplotype) | OBXs |
result (obs-complex-variant) | OBXs |
result (obs-described-variant) | OBXs |
result (obs-region-studied) | OBXs |
media | OBX? |
conclusion | OBX |
conclusionCode | OBX |
presentedForm | OBX |
Genomics Report |
DiagnosticReport | Entity. Role, or Act |
text | Act.text? |
contained | N/A |
extension | |
extension (related-artifact) | |
extension (recommended-action) | |
id | n/a |
extension | n/a |
url | N/A |
valueReference | N/A |
extension (supportingInfo) | |
id | n/a |
extension | n/a |
url | N/A |
valueReference | N/A |
extension (risk) | |
id | n/a |
url | N/A |
valueReference | N/A |
modifierExtension | N/A |
identifier | id |
basedOn | outboundRelationship[typeCode=FLFS].target |
status | statusCode Note: final and amended are distinguished by whether observation is the subject of a ControlAct event of type "revise" |
category | inboundRelationship[typeCode=COMP].source[classCode=LIST, moodCode=EVN, code < LabService].code |
code | code |
id | n/a |
extension | n/a |
coding | union(., ./translation) |
coding (code) | union(., ./translation) |
id | n/a |
extension | n/a |
system | ./codeSystem |
version | ./codeSystemVersion |
code | ./code |
display | CV.displayName |
userSelected | CD.codingRationale |
text | ./originalText[mediaType/code="text/plain"]/data |
subject | participation[typeCode=SBJ] |
encounter | inboundRelationship[typeCode=COMP].source[classCode=ENC, moodCode=EVN] |
effective[x] | effectiveTime |
issued | participation[typeCode=VRF or AUT].time |
performer | .participation[typeCode=PRF] |
resultsInterpreter | .participation[typeCode=PRF] |
specimen | participation[typeCode=SBJ] |
result | outboundRelationship[typeCode=COMP].target |
result (obs-gen-panel) | outboundRelationship[typeCode=COMP].target |
result (overall) | outboundRelationship[typeCode=COMP].target |
result (deletion-dup) | outboundRelationship[typeCode=COMP].target |
result (inh-dis-path) | outboundRelationship[typeCode=COMP].target |
result (som-diagnostic) | outboundRelationship[typeCode=COMP].target |
result (som-prognostic) | outboundRelationship[typeCode=COMP].target |
result (som-predictive) | outboundRelationship[typeCode=COMP].target |
result (med-metabolism) | outboundRelationship[typeCode=COMP].target |
result (med-efficacy) | outboundRelationship[typeCode=COMP].target |
result (med-high-risk) | outboundRelationship[typeCode=COMP].target |
result (obs-cytogenetic-nomenclature) | outboundRelationship[typeCode=COMP].target |
result (obs-genotype) | outboundRelationship[typeCode=COMP].target |
result (obs-haplotype) | outboundRelationship[typeCode=COMP].target |
result (obs-complex-variant) | outboundRelationship[typeCode=COMP].target |
result (obs-described-variant) | outboundRelationship[typeCode=COMP].target |
result (obs-region-studied) | outboundRelationship[typeCode=COMP].target |
media | outboundRelationship[typeCode=COMP].target |
id | n/a |
extension | n/a |
modifierExtension | N/A |
comment | .inboundRelationship[typeCode=COMP].source[classCode=OBS, moodCode=EVN, code="annotation"].value |
link | .value.reference |
conclusion | inboundRelationship[typeCode="SPRT"].source[classCode=OBS, moodCode=EVN, code=LOINC:48767-8].value (type=ST) |
conclusionCode | inboundRelationship[typeCode=SPRT].source[classCode=OBS, moodCode=EVN, code=LOINC:54531-9].value (type=CD) |
presentedForm | text (type=ED) |