Generated Thu Oct 26 00:18:15 UTC 2023, FHIR version 4.0.1 for hl7.fhir.us.mcode#3.0.0 (canonical = http://hl7.org/fhir/us/mcode (history)). See Full QA Report
Quality Checks | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Publisher Version: | IG Publisher Version: v1.5.0 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Publication Code: | mcode . PackageId = hl7.fhir.us.mcode, Canonical = http://hl7.org/fhir/us/mcode | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Realm Check for US: | Snomed: The IG specifies a different version (http://snomed.info/sct/900000000000207008/version/20230901) to the US edition of SNOMED CT version in the parameters ( | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Publication Request: |
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Supressed Messages: | 66 Suppressed Issues | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Dependency Checks: |
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Dependent IGs: | no references | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Global Profiles: | (none declared) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
HTA Analysis: | All OK | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
R5 Dependencies: | (none) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Draft Dependencies: |
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Modifier Extensions: | (none) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Previous Version Comparison: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
IPA Comparison: | n/a | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Summary: | errors = 17, warn = 0, info = 0, broken links = 0 |
Path | Severity | Message |
Bundle.entry[6].resource/*Observation/gx-genomic-variant-somatic-bap1-indel*/.component[2].value.ofType(CodeableConcept) (l405/c14) | error | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_004656.4:c.1768C>T) |
Bundle.entry[6].resource/*Observation/gx-genomic-variant-somatic-bap1-indel*/.component[3].value.ofType(CodeableConcept) (l424/c14) | error | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_004647.1:p.(Gln590Ter)) |
Bundle.entry[12].resource/*Observation/gx-genomic-variant-somatic-pof1b*/.component[4].value.ofType(CodeableConcept) (l1362/c14) | error | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_001307940.2:c.430C>T) |
Bundle.entry[12].resource/*Observation/gx-genomic-variant-somatic-pof1b*/.component[5].value.ofType(CodeableConcept) (l1381/c14) | error | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_001294869.1:p.(Pro144Ser)) |
Bundle.entry[13].resource/*Observation/gx-genomic-variant-somatic-polrmt*/.component[4].value.ofType(CodeableConcept) (l1571/c14) | error | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_005035.4:c.598G>A) |
Bundle.entry[13].resource/*Observation/gx-genomic-variant-somatic-polrmt*/.component[5].value.ofType(CodeableConcept) (l1590/c14) | error | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_005026.3:p.(Gly200Arg)) |
Path | Severity | Message |
Bundle.entry[7].resource/*Observation/genomic-variant-jenny-m*/.component[2].value.ofType(CodeableConcept) (l761/c14) | error | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NC_000016.10:g.23603471G>T) |
Path | Severity | Message |
Observation.component[2].value.ofType(CodeableConcept) (l75/c8) | error | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_005157.6(ABL1):c.1076T>G) |
Path | Severity | Message |
Observation.component[1].value.ofType(CodeableConcept) (l56/c8) | error | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NG_005905.2:g.126148_126152del) |
Path | Severity | Message |
Observation.component[2].value.ofType(CodeableConcept) (l76/c8) | error | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NC_000016.10:g.23603471G>T) |
Path | Severity | Message |
Observation.component[2].value.ofType(CodeableConcept) (l75/c8) | error | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_000455.5:c.725G>A) |
Path | Severity | Message |
Observation.component[2].value.ofType(CodeableConcept) (l80/c8) | error | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_004656.4:c.1768C>T) |
Observation.component[3].value.ofType(CodeableConcept) (l99/c8) | error | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_004647.1:p.(Gln590Ter)) |
Path | Severity | Message |
Observation.component[4].value.ofType(CodeableConcept) (l118/c8) | error | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_001307940.2:c.430C>T) |
Observation.component[5].value.ofType(CodeableConcept) (l137/c8) | error | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_001294869.1:p.(Pro144Ser)) |
Path | Severity | Message |
Observation.component[4].value.ofType(CodeableConcept) (l113/c8) | error | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_005035.4:c.598G>A) |
Observation.component[5].value.ofType(CodeableConcept) (l132/c8) | error | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_005026.3:p.(Gly200Arg)) |
Suppressed Messages (Warnings, hints, broken links)
DETAILS MESSAGES (THEY APPEAR TO BE FOR GROUPING PURPOSES ONLY)
IG Publisher Spurious Messages
Reference to condition-category code system is inherited from US Core and we can't change that
Reference to deprecated extension included for backwards compatibility.
Reference to work group extension value set containing "CIC" code
SUPPRESS INFORMATION MESSAGES "DOES NOT MATCH ANY KNOWN SLICE" DUE TO TERMINOLOGY LIMITATIONS
SUPPRESS US CORE COMPLIANCE WARNINGS. For STU2, exceptions to US Core parent profiles was approved by Cross-Group Projects Work Group on 1/28/2021 Floyd Eisenberg/Brett Marquard: 28-0-1. See https://jira.hl7.org/browse/FHIR-30707. For STU3, exceptions to US Core parent profiles was approved by the Cross-Group Projects Work Group on 2/9/2023 Saul Kravitz/Floyd Eisenberg: 23-0-2. See https://jira.hl7.org/browse/FHIR-40383. A variance for an additional Observation added in STU3 was approved by the Cross-Group Projects Work Group on 8/10/23. See https://jira.hl7.org/browse/FHIR-41710.
TG263 is a proprietary codesystem used in Radiotherapy. The whole point of conceptmaps is to make it easy to transition to the ValueSets used in this IG. The codesystem identifers TRX, IJE and MRE are not proper codesystem URIs. Work is underway to define proper URIs that will be included in future versions of this IG.
This is a publisher induced issue. The extension in question is introduced by the publisher, not sushi. See https://chat.fhir.org/#narrow/stream/179252-IG-creation/topic/New.20ConceptMap.20Warning.20--.20induced.20by.20IG.20Publisher
UNSUPPORTED TERMINOLOGY
Use of UCUM inherited from Genomics IG (nothing we can do about it)
Value Set Too Large to Validate
Errors sorted by type
C:\temp\hl7.fhir.us.mcode#3.0.0-milestone\fsh-generated\resources\Bundle-gx-genomic-bundle-adam-anyperson.json | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_004656.4:c.1768C>T) |
C:\temp\hl7.fhir.us.mcode#3.0.0-milestone\fsh-generated\resources\Bundle-gx-genomic-bundle-adam-anyperson.json | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_004647.1:p.(Gln590Ter)) |
C:\temp\hl7.fhir.us.mcode#3.0.0-milestone\fsh-generated\resources\Bundle-gx-genomic-bundle-adam-anyperson.json | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_001307940.2:c.430C>T) |
C:\temp\hl7.fhir.us.mcode#3.0.0-milestone\fsh-generated\resources\Bundle-gx-genomic-bundle-adam-anyperson.json | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_001294869.1:p.(Pro144Ser)) |
C:\temp\hl7.fhir.us.mcode#3.0.0-milestone\fsh-generated\resources\Bundle-gx-genomic-bundle-adam-anyperson.json | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_005035.4:c.598G>A) |
C:\temp\hl7.fhir.us.mcode#3.0.0-milestone\fsh-generated\resources\Bundle-gx-genomic-bundle-adam-anyperson.json | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_005026.3:p.(Gly200Arg)) |
C:\temp\hl7.fhir.us.mcode#3.0.0-milestone\fsh-generated\resources\Bundle-mcode-patient-bundle-jenny-m.json | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NC_000016.10:g.23603471G>T) |
C:\temp\hl7.fhir.us.mcode#3.0.0-milestone\fsh-generated\resources\Observation-genomic-variant-fusion.json | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_005157.6(ABL1):c.1076T>G) |
C:\temp\hl7.fhir.us.mcode#3.0.0-milestone\fsh-generated\resources\Observation-genomic-variant-germline-deletion.json | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NG_005905.2:g.126148_126152del) |
C:\temp\hl7.fhir.us.mcode#3.0.0-milestone\fsh-generated\resources\Observation-genomic-variant-jenny-m.json | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NC_000016.10:g.23603471G>T) |
C:\temp\hl7.fhir.us.mcode#3.0.0-milestone\fsh-generated\resources\Observation-genomic-variant-somatic-single-nucleotide.json | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_000455.5:c.725G>A) |
C:\temp\hl7.fhir.us.mcode#3.0.0-milestone\fsh-generated\resources\Observation-gx-genomic-variant-somatic-bap1-indel.json | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_004656.4:c.1768C>T) |
C:\temp\hl7.fhir.us.mcode#3.0.0-milestone\fsh-generated\resources\Observation-gx-genomic-variant-somatic-bap1-indel.json | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_004647.1:p.(Gln590Ter)) |
C:\temp\hl7.fhir.us.mcode#3.0.0-milestone\fsh-generated\resources\Observation-gx-genomic-variant-somatic-pof1b.json | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_001307940.2:c.430C>T) |
C:\temp\hl7.fhir.us.mcode#3.0.0-milestone\fsh-generated\resources\Observation-gx-genomic-variant-somatic-pof1b.json | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_001294869.1:p.(Pro144Ser)) |
C:\temp\hl7.fhir.us.mcode#3.0.0-milestone\fsh-generated\resources\Observation-gx-genomic-variant-somatic-polrmt.json | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_005035.4:c.598G>A) |
C:\temp\hl7.fhir.us.mcode#3.0.0-milestone\fsh-generated\resources\Observation-gx-genomic-variant-somatic-polrmt.json | None of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_005026.3:p.(Gly200Arg)) |