This page is part of the FHIR Specification v6.0.0-ballot1: Release 6 Ballot (1st Draft) (see Ballot Notes). The current version is 5.0.0. For a full list of available versions, see the Directory of published versions
Clinical Genomics Work Group | Maturity Level: N/A | Standards Status: Informative |
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Definition for Code SystemGenomicStudyType
@prefix fhir: <http://hl7.org/fhir/> . @prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> . # - resource ------------------------------------------------------------------- [] a fhir:CodeSystem ; fhir:id [ fhir:v "genomicstudy-type"] ; fhir:meta [ fhir:lastUpdated [ fhir:v "2023-12-17T23:12:07.602-05:00" ] ; fhir:profile ( [ fhir:v "http://hl7.org/fhir/StructureDefinition/shareablecodesystem" ] ) ] ; fhir:text [ fhir:status [ fhir:v "generated" ] ] ; fhir:extension ( [ fhir:url [ fhir:v "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg" ] ; fhir:value [ fhir:v "cg" ] ] [ fhir:url [ fhir:v "http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status" ] ; fhir:value [ fhir:v "trial-use" ] ] [ fhir:url [ fhir:v "http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm" ] ; fhir:value [ fhir:v "1" ] ] ) ; fhir:url [ fhir:v "http://hl7.org/fhir/genomicstudy-type"], [ fhir:v "http://hl7.org/fhir/genomicstudy-type"] ; fhir:identifier ( [ fhir:system [ fhir:v "urn:ietf:rfc:3986" ] ; fhir:value [ fhir:v "urn:oid:2.16.840.1.113883.4.642.4.1975" ] ] [ fhir:system [ fhir:v "urn:ietf:rfc:3986" ] ; fhir:value [ fhir:v "urn:oid:2.16.840.1.113883.4.642.4.1975" ] ] ) ; fhir:version [ fhir:v "6.0.0-ballot1"], [ fhir:v "6.0.0-ballot1"] ; fhir:name [ fhir:v "GenomicStudyType"], [ fhir:v "GenomicStudyType"] ; fhir:title [ fhir:v "Genomic Study Type"], [ fhir:v "Genomic Study Type"] ; fhir:status [ fhir:v "active"], [ fhir:v "active"] ; fhir:experimental [ fhir:v "true"], [ fhir:v "true"] ; fhir:date [ fhir:v "2022-08-17T16:19:24-05:00"], [ fhir:v "2022-08-17T16:19:24-05:00"] ; fhir:publisher [ fhir:v "HL7 (FHIR Project)"], [ fhir:v "HL7 (FHIR Project)"] ; fhir:contact ( [ fhir:telecom ( [ fhir:system [ fhir:v "url" ] ; fhir:value [ fhir:v "http://hl7.org/fhir" ] ] [ fhir:system [ fhir:v "email" ] ; fhir:value [ fhir:v "fhir@lists.hl7.org" ] ] ) ] [ fhir:telecom ( [ fhir:system [ fhir:v "url" ] ; fhir:value [ fhir:v "http://hl7.org/fhir" ] ] [ fhir:system [ fhir:v "email" ] ; fhir:value [ fhir:v "fhir@lists.hl7.org" ] ] ) ] ) ; fhir:description [ fhir:v "The type relevant to GenomicStudy."], [ fhir:v "The type relevant to GenomicStudy."] ; fhir:jurisdiction ( [ fhir:coding ( [ fhir:system [ fhir:v "http://unstats.un.org/unsd/methods/m49/m49.htm" ] ; fhir:code [ fhir:v "001" ] ; fhir:display [ fhir:v "World" ] ] ) ] [ fhir:coding ( [ fhir:system [ fhir:v "http://unstats.un.org/unsd/methods/m49/m49.htm" ] ; fhir:code [ fhir:v "001" ] ; fhir:display [ fhir:v "World" ] ] ) ] ) ; fhir:caseSensitive [ fhir:v "true"] ; fhir:valueSet [ fhir:v "http://hl7.org/fhir/ValueSet/genomicstudy-type"] ; fhir:content [ fhir:v "complete"] ; fhir:concept ( [ fhir:code [ fhir:v "alt-splc" ] ; fhir:display [ fhir:v "Alternative splicing detection" ] ; fhir:definition [ fhir:v "Identification of multiple different processed mRNA transcripts from the same DNA template" ] ] [ fhir:code [ fhir:v "chromatin" ] ; fhir:display [ fhir:v "Chromatin conformation" ] ; fhir:definition [ fhir:v "Analysis of the spacial organization of chromatin within a cell" ] ] [ fhir:code [ fhir:v "cnv" ] ; fhir:display [ fhir:v "CNV detection" ] ; fhir:definition [ fhir:v "Detection of a change in the number of copies of a defined region of genomic DNA sequence resulting in structural variation when compared to the reference sequence" ] ] [ fhir:code [ fhir:v "epi-alt-hist" ] ; fhir:display [ fhir:v "Epigenetic Alterations - histone modifications" ] ; fhir:definition [ fhir:v "Detection of biochemical modifications covalently bound to the N-terminal tail of a histone protein. These modifications may alter chromatin compaction and gene expression" ] ] [ fhir:code [ fhir:v "epi-alt-dna" ] ; fhir:display [ fhir:v "Epigenetic Alterations -DNA methylation" ] ; fhir:definition [ fhir:v "Detection of the presence of an additional methyl group on a DNA nucleobase, which may alter gene transcription" ] ] [ fhir:code [ fhir:v "fam-var-segr" ] ; fhir:display [ fhir:v "Familial variant segregation" ] ; fhir:definition [ fhir:v "Determining if a variant identified in an individual is present in other family members" ] ] [ fhir:code [ fhir:v "func-var" ] ; fhir:display [ fhir:v "Functional variation detection" ] ; fhir:definition [ fhir:v "Detection of sequence variants which may alter gene expression or gene product function when compared to the reference sequence" ] ] [ fhir:code [ fhir:v "gene-expression" ] ; fhir:display [ fhir:v "Gene expression profiling" ] ; fhir:definition [ fhir:v "Measurement and characterization of activity from all gene products" ] ] [ fhir:code [ fhir:v "post-trans-mod" ] ; fhir:display [ fhir:v "Post-translational Modification Identification" ] ; fhir:definition [ fhir:v "Detection of biochemical modifications covalently bound to the amino acid monomers of a processed protein" ] ] [ fhir:code [ fhir:v "snp" ] ; fhir:display [ fhir:v "SNP Detection" ] ; fhir:definition [ fhir:v "Determination of which nucleotide is base present at a known variable location of the genomic sequence" ] ] [ fhir:code [ fhir:v "str" ] ; fhir:display [ fhir:v "STR count" ] ; fhir:definition [ fhir:v "Quantification of the number of sequential microsatellite units in a repetitive sequence region" ] ] [ fhir:code [ fhir:v "struc-var" ] ; fhir:display [ fhir:v "Structural variation detection" ] ; fhir:definition [ fhir:v "Detection of deletions, insertions, or rearrangements of DNA segments compared to the reference sequence" ] ] ) . # -------------------------------------------------------------------------------------
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.
FHIR ®© HL7.org 2011+. FHIR R6 hl7.fhir.core#6.0.0-ballot1 generated on Mon, Dec 18, 2023 15:15+1100.
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