NHS North West Genomics
2.0.12 - ci-build United Kingdom flag

NHS North West Genomics - Local Development build (v2.0.12) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions

Table of Contents

.. 0 Table of Contents
... 1 Home
... 2 Laboratory Testing Workflow (LTW)
... 3 Inter Laboratory Workflow (ILW)
... 4 Health Data API (HIE/EURDICE)
... 5 API Security
... 6 Resource Access [IPA/QEDm]
... 7 Message Exchange [LTW/MQ]
... 8 Document Exchange [MHD]
... 9 Patient Identity Matching (PDQm)
... 10 Authorisation [IUA]
... 11 HL7 v2 Standards
... 12 Testing
... 13 Support
... 14 Overview - Data Contracts
... 15 Architecture
... 16 Architecture - Enterprise Integration Patterns (EIP)
... 17 Artifacts Summary
.... 17.1 Automation Manager
.... 17.2 Clinical Document
.... 17.3 Intermediary
.... 17.4 Order Filler
.... 17.5 Order Placer
.... 17.6 Order Result Tracker
.... 17.7 Patient Identity Source
.... 17.8 Provider Information Source
.... 17.9 Requestor (ILW)
.... 17.10 Subcontractor (ILW)
.... 17.11 CapabilityStatement for NW Genomics Genomic Data Platform (EURIDICE Health Data API)
.... 17.12 CapabilityStatement for NW GMSA Regional Orchestration Engine for Genomics
.... 17.13 Process Message
.... 17.14 Message Definition - Acknowledgement
.... 17.15 Message Definition - Document and Document Notification
.... 17.16 Message Definition - Laboratory Order
.... 17.17 Message Definition - Unsolicited Observation
.... 17.18 assigner
.... 17.19 CBC panel - Blood by Automated count
.... 17.20 Comprehensive metabolic 2000 panel - Serum or Plasma
.... 17.21 Master HL7 genetic variant reporting panel
.... 17.22 North West Genomics Test Order
.... 17.23 North West Genomics Test Report
.... 17.24 Pedigree
.... 17.25 AuditEvent
.... 17.26 Binary
.... 17.27 Bundle - FHIR Document
.... 17.28 Bundle - FHIR Messaging
.... 17.29 Composition Genomic Report
.... 17.30 Condition
.... 17.31 Diagnostic Implication (Observation)
.... 17.32 Diagnostic Report
.... 17.33 Document Message (MessageHeader)
.... 17.34 DocumentReference
.... 17.35 Encounter
.... 17.36 Event Notification (MessageHeader)
.... 17.37 FamilyMemberHistory
.... 17.38 Genomic Observation
.... 17.39 Genomic Study (Observation Panel)
.... 17.40 Genomic Study (Procedure)
.... 17.41 Genotype (Observation)
.... 17.42 Hospital Spell
.... 17.43 Laboratory Analyte Result (Observation)
.... 17.44 Molecular Biomarker
.... 17.45 Observation
.... 17.46 Observation Order
.... 17.47 Observation Panel
.... 17.48 OperationOutcome
.... 17.49 Organization
.... 17.50 Patient
.... 17.51 Practitioner
.... 17.52 PractitionerRole
.... 17.53 Procedure
.... 17.54 Questionnaire
.... 17.55 QuestionnaireResponse
.... 17.56 RelatedPerson
.... 17.57 ServiceRequest
.... 17.58 Specimen
.... 17.59 Task
.... 17.60 Therapeutic Implication (Observation)
.... 17.61 Variant (Observation)
.... 17.62 Visit
.... 17.63 WorkOrder
.... 17.64 Attachment
.... 17.65 CodeableReference
.... 17.66 Correlation Identifier
.... 17.67 Genomics Pedigree Number
.... 17.68 GS1 Global Service Relation Number (GSRN)
.... 17.69 GS1 Serial Shipping Container Code (SSCC)
.... 17.70 GS1 Service Relation Instance Number (SRIN)
.... 17.71 Hospital Provider Spell Identifier
.... 17.72 Medical Record Number
.... 17.73 Medical Record Number
.... 17.74 NHS Identifier
.... 17.75 Order Group Number
.... 17.76 Order Identifier
.... 17.77 Organisation Code
.... 17.78 Organisation Site Identifier
.... 17.79 Practitioner Identifier
.... 17.80 Report Identifier
.... 17.81 Shipment Tracking Number
.... 17.82 Specimen Accession Number
.... 17.83 Visit Number
.... 17.84 ExtCodeableReference
.... 17.85 Admission Method
.... 17.86 Admission Source
.... 17.87 Discharge Destination
.... 17.88 Discharge Disposition
.... 17.89 DocumentEntry Class
.... 17.90 DocumentEntry mimeType
.... 17.91 DocumentEntry Type
.... 17.92 Ethnicity
.... 17.93 Facility Type
.... 17.94 Genomic Cancer Test Directory
.... 17.95 Genomic Clinical Indication Codes
.... 17.96 Genomic Disorder Carrier
.... 17.97 Genomic Finding
.... 17.98 Genomic Finding Detected
.... 17.99 Genomic Rare and Inherited Disease Test Directory
.... 17.100 Genomic Test Codes
.... 17.101 Genomic Test Outcome Codes
.... 17.102 NW IdentifierType
.... 17.103 Order Category
.... 17.104 Organisation Cheshire and Merseyside ICS (QYG) NHS Trusts
.... 17.105 Organisation Greater Manchester ICS (QOP) NHS Trusts
.... 17.106 Organisation Lancashire and South Cumbria ICS (QE1) NHS Trusts
.... 17.107 Organisation North West Region NHS Trusts
.... 17.108 Patient Encounter Trigger
.... 17.109 Patient Identity Trigger
.... 17.110 Practitioner Identifiers
.... 17.111 Pregnancy
.... 17.112 Request Priority
.... 17.113 Service
.... 17.114 Specialty
.... 17.115 Specimen Body Site
.... 17.116 Specimen Tracking Events
.... 17.117 Specimen Type
.... 17.118 UK National Health Identifiers
.... 17.119 Yes/No
.... 17.120 Yes/No/Unknown
.... 17.121 CodeSystem for Analyser
.... 17.122 CodeSystem not defined or to be determined
.... 17.123 iGene Codes
.... 17.124 iGene Sample Sub Type
.... 17.125 iGene Test Codes
.... 17.126 MFT EPIC Question Ids
.... 17.127 NHS England Genomic Clinical Indication Code
.... 17.128 NHS England Genomic Test Code
.... 17.129 NHS England Genomic Test Outcome Code
.... 17.130 North West Genomics Test Code
.... 17.131 NW GMSA Codes
.... 17.132 Task Input/Output Parameter Type
.... 17.133 UK National Health Identifiers
.... 17.134 UK Professional License
.... 17.135 GMC Number
.... 17.136 GMP Number
.... 17.137 NHS Number
.... 17.138 ODS Code
.... 17.139 ODS Site Code
.... 17.140 LOINC to SNOMED UK edition
.... 17.141 Sample Body Site (SNOMED) to iGene Specimen Sub Type
.... 17.142 Sample Type (SNOMED) to iGene Specimen Type
.... 17.143 SNOMED LOINC edition to SNOMED UK edition
.... 17.144 Clinical and Genomic Workflow
.... 17.145 Collect Specimen - Biopsy Procedure for obtaining a specimen, part of a diagnostic pathway. Day case admission.
.... 17.146 Genomic Test Order Process including order entry and transmission of the order
.... 17.147 Genomic Test Report Process
.... 17.148 AuditEvent Mobile Query Existing Data [PCC-44]
.... 17.149 AuditEvent Placer Order Management [LAB-1] V2/FHIR/V2 Order
.... 17.150 Bundle 'Event Message' - Patient Update
.... 17.151 Bundle 'Message' - Genomics Order Reply
.... 17.152 Bundle 'Message' - Genomics Order Reply Acknowledgement
.... 17.153 Bundle 'Transaction' - Genomics Order Asynchronous Message Reply Acknowledgement
.... 17.154 Bundle - Conditions for a Patient QEDm
.... 17.155 Bundle - Form Search Results SDC
.... 17.156 Bundle - Genomic Diagnostic Implication for a Patient QEDm
.... 17.157 Bundle - Genomic Variant for a Patient QEDm
.... 17.158 Bundle - Genomic Variant Gene = NTHL1 QEDm
.... 17.159 Bundle - Patient Search Results by Medical Record Number PDQ
.... 17.160 Bundle - Patient Search Results by NHS Number PDQ
.... 17.161 Condition - Carcinoma
.... 17.162 Condition - Lynch Syndrome
.... 17.163 Consanguinity (type=CE)
.... 17.164 Example Document and Document Notification Message
.... 17.165 Example of a Message Acknowledgement
.... 17.166 Example of a Message Search
.... 17.167 FamilyMemberHistory - Ricky LEEDS
.... 17.168 FamilyMemberHistory - Sarah-Jane Nottingham
.... 17.169 FHIR RESTful POST ServiceRequest
.... 17.170 Genomic Report BRCA1 Variant Example
.... 17.171 Genomic Report Ovarian Carcinoma Diagnostic Implication Example
.... 17.172 Genomic Study (Panel) - Cystic Fibrosis
.... 17.173 Genomic Study (Panel) - Lynch Syndrome
.... 17.174 Laboratory Analyte Result BCRABL Invalid Example
.... 17.175 Laboratory Analyte Result BCRABL Valid Example
.... 17.176 MCV - Mean corpuscular volume
.... 17.177 Message Header - Genomic Order Reply fatal
.... 17.178 Message Header - Genomic Order Reply fatal Acknowledgement
.... 17.179 Message Header - Genomic Order Reply Transient
.... 17.180 Message Header - Genomic Report
.... 17.181 Message Header - Patient
.... 17.182 Observation - Lynch Syndrome Mutation Finding
.... 17.183 Order Tracking Number (type=ST)
.... 17.184 Organization MANCHESTER UNIVERSITY NHS FOUNDATION TRUST
.... 17.185 Organization North West GMSA
.... 17.186 Output from a FHIR Validation
.... 17.187 Parameters Expansion Profile
.... 17.188 Patient - Birmingham
.... 17.189 Patient - Bolton
.... 17.190 Patient - Congleton
.... 17.191 Patient - Fetus London
.... 17.192 Patient - Lancaster
.... 17.193 Patient - London
.... 17.194 Patient - Ned Liverpool NHS Number: 9737383206
.... 17.195 Patient - Northwich
.... 17.196 Patient - Nottingham
.... 17.197 Patient - Rob Leeds NHS Number: 9737383222
.... 17.198 Patient - Sansa Manchester NHS Number: 9737383192
.... 17.199 Patient - Warrington
.... 17.200 Patient - Wrexham
.... 17.201 PractitionerRole Result INTERPRETER
.... 17.202 Pregnancy Expected Delivery Date (type=DT)
.... 17.203 Procedure - Liver Biopsy
.... 17.204 RelatedPerson Birmingham-Lancaster
.... 17.205 RelatedPerson Birmingham-London
.... 17.206 RelatedPerson Lancaster-London
.... 17.207 RelatedPerson London-Lancaster
.... 17.208 RelatedPerson Mother Cersei London
.... 17.209 RelatedPerson Wrexham-Lancaster
.... 17.210 RelatedPerson Wrexham-London
.... 17.211 Task Genomic Test Completed
.... 17.212 Task Genomic Test Requested
.... 17.213 Binary Genomic Record of Discussion Example
.... 17.214 Bundle 'Message' - Genomics Order Reply
.... 17.215 Bundle 'Message' - Genomics Order with Attachment
.... 17.216 Bundle 'Message' - Genomics Order with Coded Entries
.... 17.217 Bundle 'SearchSet' - Genomics Order
.... 17.218 Document Reference Laboratory Order
.... 17.219 Encounter 'episode/stay' Example
.... 17.220 Message Header - Genomic Order
.... 17.221 Message Header - Genomic Order Reply ok
.... 17.222 Patient - OctaviaCHISLETT NHS Number: 9449305552
.... 17.223 PractitionerRole C3456789 Example
.... 17.224 ServiceRequest Attachment Example
.... 17.225 ServiceRequest Coded Entries Example
.... 17.226 Specimen Example
.... 17.227 Binary Genomic Report Example
.... 17.228 Bundle 'Message' - Genomics Report
.... 17.229 Diagnostic Report Example.
.... 17.230 Document Reference Laboratory Report
.... 17.231 Message Header - Genomic Report
.... 17.232 DiagnosticImplication - Cystic Fibrosis Carrier
.... 17.233 DiagnosticImplication - Lynch Syndrome
.... 17.234 Genomic Study - Cystic Fibrosis
.... 17.235 Genomic Study - Lynch Syndrome
.... 17.236 Variant - CFTR
.... 17.237 Variant - NTHL1
.... 17.238 748683741
.... 17.239 Bundle `Document` - Genomics Report
.... 17.240 Composition - Genomics Report Octavia CHISLETT
.... 17.241 EPIC-OBR-1 Example
.... 17.242 EPIC-OBX-10 Example
.... 17.243 EPIC-OBX-11 Example
.... 17.244 EPIC-OBX-2 Example
.... 17.245 EPIC-OBX-4 Example
.... 17.246 EPIC-OBX-6 Example
.... 17.247 EPIC-OBX-7 Example
.... 17.248 EPIC-OBX-8 Example
.... 17.249 Genomic Referral Category
.... 17.250 High infection risk sample
.... 17.251 Informed Consent
.... 17.252 OBX Pregnancy
.... 17.253 Supervising Clinician
.... 17.254 Bundle-Bundle-NonWGSTestOrderForm-Reanalysis-Example
.... 17.255 Bundle-NonWGSTestOrderForm-CancerSolidTumor-Example
.... 17.256 Bundle-NonWGSTestOrderForm-FetalScenario-Example
.... 17.257 NRL Genomic Report for Cersei LONDON (Test NHS Number 9737383230). Original order electronic from EPIC system
.... 17.258 NRL Genomic Report for Tommen BIRMINGHAM (Test NHS Number 9737383249). Original order not electronic
.... 17.259 837d78a0-30cd-478c-83a8-f83d16fc4443