Generated Tue Apr 09 14:01:31 UTC 2024 for hl7.fhir.uv.genomics-reporting
| id | published | ballot | current |
| hl7.fhir.us.mcode | 2.0.0 | 2.0.0 |
Derived profiles
| Variant | Genomic Variant Profile |
| ClinVar Evidence Level Example Codes | (not used) |
| Coded Annotation Type Codes | (not used) |
| Genomic Study Change Type CodeSystem | (not used) |
| Genomic Study Data Format CodeSystem | (not used) |
| Genomic Study Method Type CodeSystem | (not used) |
| Genomic Study Status CodeSystem | (not used) |
| Genomic Study Type CodeSystem | (not used) |
| Molecular Biomarker Ontology Codes | (not used) |
| PharmGKB Evidence Level Example Codes | (not used) |
| Sequence Phase Relationship Codes | (not used) |
| To Be Determined Codes | (not used) |
| Variant Confidence Status Codes | (not used) |
| Coded Annotation Types | (not used) |
| Condition Inheritance Patterns | (not used) |
| DNA Change Type | (not used) |
| Evidence Level Examples | (not used) |
| Functional Effect Value Set | (not used) |
| Genetic Therapeutic Implications | (not used) |
| Genomic Study Change Type ValueSet | (not used) |
| Genomic Study Data Format ValueSet | (not used) |
| Genomic Study Method Type ValueSet | (not used) |
| Genomic Study Status ValueSet | (not used) |
| Genomic Study Type ValueSet | (not used) |
| HUGO Gene Nomenclature Committee Gene Names (HGNC) | (not used) |
| Human Genome Variation Society (HGVS) Nomenclature | (not used) |
| High Low codes | (not used) |
| Molecular Biomarker Categories | (not used) |
| Molecular Biomarker Codes | (not used) |
| Molecular Consequence Value Set | (not used) |
| Sequence Phase Relationships | (not used) |
| To Be Determined Value Set | (not used) |
| Variant Confidence Status | (not used) |
| Coded Annotation | (not used) |
| Diagnostic Implication | (not used) |
| Genomic Finding | (not used) |
| Followup Recommendation | (not used) |
| Genomic Base | (not used) |
| Genomic Data File | (not used) |
| Genomic Report | (not used) |
| Genomic Study | (not used) |
| Genomic Study Analysis | (not used) |
| Genotype | (not used) |
| Haplotype | (not used) |
| Genomic Implication | (not used) |
| Medication Recommendation | (not used) |
| Molecular Biomarker | (not used) |
| Molecular Consequence | (not used) |
| Sequence Phase Relationship | (not used) |
| Therapeutic Implication | (not used) |
| Variant | Constrained In Genomic Variant Profile (hl7.fhir.us.mcode) |
| Annotation Code | (not used) |
| Genomic Report Note | (not used) |
| Genomic Risk Assessment | (not used) |
| Genomic Study Analysis Change Type | (not used) |
| Genomic Study Analysis Device | (not used) |
| Genomic Study Analysis Extension | (not used) |
| Genomic Study Analysis Focus | (not used) |
| Genomic Study Analysis Genome Build | (not used) |
| Genomic Study Analysis Input | (not used) |
| Genomic Study Analysis Method Type | (not used) |
| Genomic Study Analysis Metrics | (not used) |
| Genomic Study Analysis Output | (not used) |
| Genomic Study Analysis Protocol Performed | (not used) |
| Genomic Study Analysis Regions | (not used) |
| Genomic Study Analysis Specimen | (not used) |
| Genomic Study Analysis Title | (not used) |
| Genomic Study Reference | (not used) |
| Genomic Study Referrer Extension | (not used) |
| Medication Assessed reference to a FHIR resource | (not used) |
| Recommended Action | (not used) |
| Related Artifact for Observation component | (not used) |
| Repeat Motif Order | (not used) |
| Therapy Assessed reference to a FHIR resource | (not used) |