Mappings for the fujitsu-observation-genomic-variant resource profile.
FujitsuObservationGenomicVariant |
Observation | < 363787002 |Observable entity| |
status | < 445584004 |Report by finality status| |
code | < 363787002 |Observable entity| OR < 386053000 |Evaluation procedure| |
value[x] | < 441742003 |Evaluation finding| |
value[x] (valueCodeableConcept) | < 441742003 |Evaluation finding| |
specimen | < 123038009 |Specimen| |
component | |
code | < 363787002 |Observable entity| OR
< 386053000 |Evaluation procedure| |
value[x] | 363714003 |Interprets| < 441742003 |Evaluation finding| |
interpretation | < 260245000 |Findings values| |
component (gene-studied) | |
code | < 363787002 |Observable entity| OR
< 386053000 |Evaluation procedure| |
value[x] | 363714003 |Interprets| < 441742003 |Evaluation finding| |
component (cytogenetic-location) | |
code | < 363787002 |Observable entity| OR
< 386053000 |Evaluation procedure| |
value[x] | 363714003 |Interprets| < 441742003 |Evaluation finding| |
component (genomic-hgvs) | |
code | < 363787002 |Observable entity| OR
< 386053000 |Evaluation procedure| |
value[x] | 363714003 |Interprets| < 441742003 |Evaluation finding| |
component (cytogenomic-nomenclature) | |
code | < 363787002 |Observable entity| OR
< 386053000 |Evaluation procedure| |
value[x] | 363714003 |Interprets| < 441742003 |Evaluation finding| |
component (coding-change-type) | |
code | < 363787002 |Observable entity| OR
< 386053000 |Evaluation procedure| |
value[x] | 363714003 |Interprets| < 441742003 |Evaluation finding| |
component (genomic-source-class) | |
code | < 363787002 |Observable entity| OR
< 386053000 |Evaluation procedure| |
value[x] | 363714003 |Interprets| < 441742003 |Evaluation finding| |
component (sample-allelic-frequency) | |
code | < 363787002 |Observable entity| OR
< 386053000 |Evaluation procedure| |
value[x] | 363714003 |Interprets| < 441742003 |Evaluation finding| |
component (allelic-state) | |
code | < 363787002 |Observable entity| OR
< 386053000 |Evaluation procedure| |
value[x] | 363714003 |Interprets| < 441742003 |Evaluation finding| |
component (variation-code) | |
code | < 363787002 |Observable entity| OR
< 386053000 |Evaluation procedure| |
value[x] | 363714003 |Interprets| < 441742003 |Evaluation finding| |
component (protein-hgvs) | |
code | < 363787002 |Observable entity| OR
< 386053000 |Evaluation procedure| |
value[x] | 363714003 |Interprets| < 441742003 |Evaluation finding| |
component (amino-acid-change-type) | |
code | < 363787002 |Observable entity| OR
< 386053000 |Evaluation procedure| |
value[x] | 363714003 |Interprets| < 441742003 |Evaluation finding| |
component (molecular-consequence) | |
code | < 363787002 |Observable entity| OR
< 386053000 |Evaluation procedure| |
value[x] | 363714003 |Interprets| < 441742003 |Evaluation finding| |
component (copy-number) | |
code | < 363787002 |Observable entity| OR
< 386053000 |Evaluation procedure| |
value[x] | 363714003 |Interprets| < 441742003 |Evaluation finding| |
FujitsuObservationGenomicVariant |
Observation | OBX |
identifier | OBX.21 For OBX segments from systems without OBX-21 support a combination of ORC/OBR and OBX must be negotiated between trading partners to uniquely identify the OBX segment. Depending on how V2 has been implemented each of these may be an option: 1) OBR-3 + OBX-3 + OBX-4 or 2) OBR-3 + OBR-4 + OBX-3 + OBX-4 or 2) some other way to uniquely ID the OBR/ORC + OBX-3 + OBX-4. |
status | OBX-11 |
category | |
category (labCategory) | |
coding | C*E.1-8, C*E.10-22 |
system | C*E.3 |
code | C*E.1 |
display | C*E.2 - but note this is not well followed |
text | C*E.9. But note many systems use C*E.2 for this |
code | OBX-3 |
coding | C*E.1-8, C*E.10-22 |
system | C*E.3 |
code | C*E.1 |
display | C*E.2 - but note this is not well followed |
text | C*E.9. But note many systems use C*E.2 for this |
subject | PID-3 |
effective[x] | OBX-14, and/or OBX-19 after v2.4 (depends on who observation made) |
value[x] | OBX.2, OBX.5, OBX.6 |
value[x] (valueCodeableConcept) | OBX.2, OBX.5, OBX.6 |
dataAbsentReason | N/A |
method | OBX-17 |
specimen | SPM segment |
component | containment by OBX-4? |
code | OBX-3 |
value[x] | OBX.2, OBX.5, OBX.6 |
dataAbsentReason | N/A |
interpretation | OBX-8 |
referenceRange | OBX.7 |
component (gene-studied) | containment by OBX-4? |
code | OBX-3 |
coding | C*E.1-8, C*E.10-22 |
system | C*E.3 |
code | C*E.1 |
display | C*E.2 - but note this is not well followed |
text | C*E.9. But note many systems use C*E.2 for this |
value[x] | OBX.2, OBX.5, OBX.6 |
dataAbsentReason | N/A |
component (cytogenetic-location) | containment by OBX-4? |
code | OBX-3 |
coding | C*E.1-8, C*E.10-22 |
system | C*E.3 |
code | C*E.1 |
display | C*E.2 - but note this is not well followed |
text | C*E.9. But note many systems use C*E.2 for this |
value[x] | OBX.2, OBX.5, OBX.6 |
dataAbsentReason | N/A |
component (genomic-hgvs) | containment by OBX-4? |
code | OBX-3 |
coding | C*E.1-8, C*E.10-22 |
system | C*E.3 |
code | C*E.1 |
display | C*E.2 - but note this is not well followed |
text | C*E.9. But note many systems use C*E.2 for this |
value[x] | OBX.2, OBX.5, OBX.6 |
dataAbsentReason | N/A |
component (cytogenomic-nomenclature) | containment by OBX-4? |
code | OBX-3 |
coding | C*E.1-8, C*E.10-22 |
system | C*E.3 |
code | C*E.1 |
display | C*E.2 - but note this is not well followed |
text | C*E.9. But note many systems use C*E.2 for this |
value[x] | OBX.2, OBX.5, OBX.6 |
dataAbsentReason | N/A |
component (coding-change-type) | containment by OBX-4? |
code | OBX-3 |
coding | C*E.1-8, C*E.10-22 |
system | C*E.3 |
code | C*E.1 |
display | C*E.2 - but note this is not well followed |
text | C*E.9. But note many systems use C*E.2 for this |
value[x] | OBX.2, OBX.5, OBX.6 |
dataAbsentReason | N/A |
component (genomic-source-class) | containment by OBX-4? |
code | OBX-3 |
coding | C*E.1-8, C*E.10-22 |
system | C*E.3 |
code | C*E.1 |
display | C*E.2 - but note this is not well followed |
text | C*E.9. But note many systems use C*E.2 for this |
value[x] | OBX.2, OBX.5, OBX.6 |
dataAbsentReason | N/A |
component (sample-allelic-frequency) | containment by OBX-4? |
code | OBX-3 |
coding | C*E.1-8, C*E.10-22 |
system | C*E.3 |
code | C*E.1 |
display | C*E.2 - but note this is not well followed |
text | C*E.9. But note many systems use C*E.2 for this |
value[x] | OBX.2, OBX.5, OBX.6 |
value | SN.2 / CQ - N/A |
comparator | SN.1 / CQ.1 |
unit | (see OBX.6 etc.) / CQ.2 |
system | (see OBX.6 etc.) / CQ.2 |
code | (see OBX.6 etc.) / CQ.2 |
dataAbsentReason | N/A |
component (allelic-state) | containment by OBX-4? |
code | OBX-3 |
coding | C*E.1-8, C*E.10-22 |
system | C*E.3 |
code | C*E.1 |
display | C*E.2 - but note this is not well followed |
text | C*E.9. But note many systems use C*E.2 for this |
value[x] | OBX.2, OBX.5, OBX.6 |
dataAbsentReason | N/A |
component (variation-code) | containment by OBX-4? |
code | OBX-3 |
coding | C*E.1-8, C*E.10-22 |
system | C*E.3 |
code | C*E.1 |
display | C*E.2 - but note this is not well followed |
text | C*E.9. But note many systems use C*E.2 for this |
value[x] | OBX.2, OBX.5, OBX.6 |
dataAbsentReason | N/A |
component (protein-hgvs) | containment by OBX-4? |
code | OBX-3 |
coding | C*E.1-8, C*E.10-22 |
system | C*E.3 |
code | C*E.1 |
display | C*E.2 - but note this is not well followed |
text | C*E.9. But note many systems use C*E.2 for this |
value[x] | OBX.2, OBX.5, OBX.6 |
dataAbsentReason | N/A |
component (amino-acid-change-type) | containment by OBX-4? |
code | OBX-3 |
coding | C*E.1-8, C*E.10-22 |
system | C*E.3 |
code | C*E.1 |
display | C*E.2 - but note this is not well followed |
text | C*E.9. But note many systems use C*E.2 for this |
value[x] | OBX.2, OBX.5, OBX.6 |
dataAbsentReason | N/A |
component (molecular-consequence) | containment by OBX-4? |
code | OBX-3 |
coding | C*E.1-8, C*E.10-22 |
system | C*E.3 |
code | C*E.1 |
display | C*E.2 - but note this is not well followed |
text | C*E.9. But note many systems use C*E.2 for this |
value[x] | OBX.2, OBX.5, OBX.6 |
dataAbsentReason | N/A |
component (copy-number) | containment by OBX-4? |
code | OBX-3 |
coding | C*E.1-8, C*E.10-22 |
system | C*E.3 |
code | C*E.1 |
display | C*E.2 - but note this is not well followed |
text | C*E.9. But note many systems use C*E.2 for this |
value[x] | OBX.2, OBX.5, OBX.6 |
dataAbsentReason | N/A |
FujitsuObservationGenomicVariant |
Observation | Entity. Role, or Act, Observation[classCode=OBS, moodCode=EVN] |
text | Act.text? |
contained | N/A |
identifier | id |
status | status Amended & Final are differentiated by whether it is the subject of a ControlAct event with a type of "revise" |
category | .outboundRelationship[typeCode="COMP].target[classCode="LIST", moodCode="EVN"].code |
category (labCategory) | .outboundRelationship[typeCode="COMP].target[classCode="LIST", moodCode="EVN"].code |
coding | union(., ./translation) |
system | ./codeSystem |
code | ./code |
display | CV.displayName |
text | ./originalText[mediaType/code="text/plain"]/data |
code | code |
coding | union(., ./translation) |
system | ./codeSystem |
code | ./code |
display | CV.displayName |
text | ./originalText[mediaType/code="text/plain"]/data |
subject | participation[typeCode=RTGT] |
reference | N/A |
identifier | .identifier |
effective[x] | effectiveTime |
value[x] | value |
value[x] (valueCodeableConcept) | value |
dataAbsentReason | value.nullFlavor |
method | methodCode |
specimen | participation[typeCode=SPC].specimen |
reference | N/A |
identifier | .identifier |
component | outBoundRelationship[typeCode=COMP] |
id | n/a |
extension | n/a |
modifierExtension | N/A |
code | code |
value[x] | value |
dataAbsentReason | value.nullFlavor |
interpretation | interpretationCode |
referenceRange | outboundRelationship[typeCode=REFV]/target[classCode=OBS, moodCode=EVN] |
component (gene-studied) | outBoundRelationship[typeCode=COMP] |
id | n/a |
code | code |
coding | union(., ./translation) |
system | ./codeSystem |
code | ./code |
display | CV.displayName |
text | ./originalText[mediaType/code="text/plain"]/data |
value[x] | value |
dataAbsentReason | value.nullFlavor |
component (cytogenetic-location) | outBoundRelationship[typeCode=COMP] |
id | n/a |
code | code |
coding | union(., ./translation) |
system | ./codeSystem |
code | ./code |
display | CV.displayName |
text | ./originalText[mediaType/code="text/plain"]/data |
value[x] | value |
dataAbsentReason | value.nullFlavor |
component (genomic-hgvs) | outBoundRelationship[typeCode=COMP] |
id | n/a |
code | code |
coding | union(., ./translation) |
system | ./codeSystem |
code | ./code |
display | CV.displayName |
text | ./originalText[mediaType/code="text/plain"]/data |
value[x] | value |
dataAbsentReason | value.nullFlavor |
component (cytogenomic-nomenclature) | outBoundRelationship[typeCode=COMP] |
id | n/a |
code | code |
coding | union(., ./translation) |
system | ./codeSystem |
code | ./code |
display | CV.displayName |
text | ./originalText[mediaType/code="text/plain"]/data |
value[x] | value |
dataAbsentReason | value.nullFlavor |
component (coding-change-type) | outBoundRelationship[typeCode=COMP] |
id | n/a |
code | code |
coding | union(., ./translation) |
system | ./codeSystem |
code | ./code |
display | CV.displayName |
text | ./originalText[mediaType/code="text/plain"]/data |
value[x] | value |
dataAbsentReason | value.nullFlavor |
component (genomic-source-class) | outBoundRelationship[typeCode=COMP] |
id | n/a |
code | code |
coding | union(., ./translation) |
system | ./codeSystem |
code | ./code |
display | CV.displayName |
text | ./originalText[mediaType/code="text/plain"]/data |
value[x] | value |
dataAbsentReason | value.nullFlavor |
component (sample-allelic-frequency) | outBoundRelationship[typeCode=COMP] |
id | n/a |
code | code |
coding | union(., ./translation) |
system | ./codeSystem |
code | ./code |
display | CV.displayName |
text | ./originalText[mediaType/code="text/plain"]/data |
value[x] | value |
id | n/a |
extension | n/a |
value | PQ.value, CO.value, MO.value, IVL.high or IVL.low depending on the value |
comparator | IVL properties |
unit | PQ.unit |
system | CO.codeSystem, PQ.translation.codeSystem |
code | PQ.code, MO.currency, PQ.translation.code |
dataAbsentReason | value.nullFlavor |
component (allelic-state) | outBoundRelationship[typeCode=COMP] |
id | n/a |
code | code |
coding | union(., ./translation) |
system | ./codeSystem |
code | ./code |
display | CV.displayName |
text | ./originalText[mediaType/code="text/plain"]/data |
value[x] | value |
dataAbsentReason | value.nullFlavor |
component (variation-code) | outBoundRelationship[typeCode=COMP] |
id | n/a |
code | code |
coding | union(., ./translation) |
system | ./codeSystem |
code | ./code |
display | CV.displayName |
text | ./originalText[mediaType/code="text/plain"]/data |
value[x] | value |
dataAbsentReason | value.nullFlavor |
component (protein-hgvs) | outBoundRelationship[typeCode=COMP] |
id | n/a |
code | code |
coding | union(., ./translation) |
system | ./codeSystem |
code | ./code |
display | CV.displayName |
text | ./originalText[mediaType/code="text/plain"]/data |
value[x] | value |
dataAbsentReason | value.nullFlavor |
component (amino-acid-change-type) | outBoundRelationship[typeCode=COMP] |
id | n/a |
code | code |
coding | union(., ./translation) |
system | ./codeSystem |
code | ./code |
display | CV.displayName |
text | ./originalText[mediaType/code="text/plain"]/data |
value[x] | value |
dataAbsentReason | value.nullFlavor |
component (molecular-consequence) | outBoundRelationship[typeCode=COMP] |
id | n/a |
code | code |
coding | union(., ./translation) |
system | ./codeSystem |
code | ./code |
display | CV.displayName |
text | ./originalText[mediaType/code="text/plain"]/data |
value[x] | value |
dataAbsentReason | value.nullFlavor |
component (copy-number) | outBoundRelationship[typeCode=COMP] |
id | n/a |
code | code |
coding | union(., ./translation) |
system | ./codeSystem |
code | ./code |
display | CV.displayName |
text | ./originalText[mediaType/code="text/plain"]/data |
value[x] | value |
dataAbsentReason | value.nullFlavor |
FujitsuObservationGenomicVariant |
Observation | |
code | 116680003 |Is a| |
value[x] | 363714003 |Interprets| |
value[x] (valueCodeableConcept) | 363714003 |Interprets| |
specimen | 704319004 |Inherent in| |
component | |
value[x] | 363714003 |Interprets| |
interpretation | 363713009 |Has interpretation| |
component (gene-studied) | |
value[x] | 363714003 |Interprets| |
component (cytogenetic-location) | |
value[x] | 363714003 |Interprets| |
component (genomic-hgvs) | |
value[x] | 363714003 |Interprets| |
component (cytogenomic-nomenclature) | |
value[x] | 363714003 |Interprets| |
component (coding-change-type) | |
value[x] | 363714003 |Interprets| |
component (genomic-source-class) | |
value[x] | 363714003 |Interprets| |
component (sample-allelic-frequency) | |
value[x] | 363714003 |Interprets| |
component (allelic-state) | |
value[x] | 363714003 |Interprets| |
component (variation-code) | |
value[x] | 363714003 |Interprets| |
component (protein-hgvs) | |
value[x] | 363714003 |Interprets| |
component (amino-acid-change-type) | |
value[x] | 363714003 |Interprets| |
component (molecular-consequence) | |
value[x] | 363714003 |Interprets| |
component (copy-number) | |
value[x] | 363714003 |Interprets| |