 0 Table of Contents |
  1 Home |
  2 Business Analysis |
  3 Laboratory Testing Workflow (LTW) |
  4 Patient Administration (PAM) |
  5 Laboratory Specimen Barcode Labeling (LBL) |
  6 Healthcare Provider Directory (HPD) |
  7 Genomic Archiving and Communication System (GACS) |
  8 Health Document Sharing (MHDS) and Sharing Laboratory Reports (XD-LAB) |
  9 Placer Order Management [LAB-1] |
  10 Filler Order Management [LAB-2] |
  11 Order Results Management [LAB-3] |
  12 Work Order Management [LAB-4] |
  13 Test Results Management [LAB-5] |
  14 Query Existing Data [QEDm] |
  15 Mobile Access to Health Documents [MHD] |
  16 Patient Demographics Query for Mobile (PDQm) |
  17 Overview |
  18 HL7 v2 Standards |
  19 Architecture |
  20 Testing |
  21 Support |
  22 API Security |
  23 Deployment |
  24 Delivery Overview |
  25 OAuth2 |
  26 Workflow/Interaction Options |
  27 Genomic Report Sharing Options |
  28 Identifiers and Codes |
  29 Data Contracts and Issue Reporting |
  30 Care Services Discovery |
  31 Specimen Event Tracking (SET) |
  32 Inter Laboratory Workflow (ILW) |
  33 Simple |
  34 Digital Consent (IHE BPPC and PCF) |
  35 Design |
  36 Exchange |
  37 Artifacts Summary |
   37.1 Automation Manager |
   37.2 Clinical Document |
   37.3 Intermediary |
   37.4 Order Filler |
   37.5 Order Placer |
   37.6 Order Result Tracker |
   37.7 Patient Identity Source |
   37.8 Provider Information Source |
   37.9 Requestor (ILW) |
   37.10 Subcontractor (ILW) |
   37.11 CapabilityStatement for NW Genomics Genomic Data Repository (EURIDICE Health Data API) |
   37.12 CapabilityStatement for NW GMSA Regional Orchestration Engine for Genomics |
   37.13 Process Message |
   37.14 Message Definition - Laboratory Order |
   37.15 Message Definition - Patient Encounter |
   37.16 Message Definition - Patient Identity |
   37.17 Message Definition - Unsolicited Observation |
   37.18 assigner |
   37.19 CBC panel - Blood by Automated count |
   37.20 Comprehensive metabolic 2000 panel - Serum or Plasma |
   37.21 Master HL7 genetic variant reporting panel |
   37.22 North West Genomics Test Order |
   37.23 North West Genomics Test Order Future |
   37.24 North West Genomics Test Report |
   37.25 Pedigree |
   37.26 AuditEvent |
   37.27 Binary |
   37.28 Composition Genomic Report |
   37.29 Condition |
   37.30 Diagnostic Implication (Observation) |
   37.31 Diagnostic Report |
   37.32 Document Message (MessageHeader) |
   37.33 DocumentReference |
   37.34 Encounter |
   37.35 Event Notification (MessageHeader) |
   37.36 FamilyMemberHistory |
   37.37 Genomic Study (Observation Panel) |
   37.38 Genomic Study (Procedure) |
   37.39 Genotype (Observation) |
   37.40 Hospital Spell |
   37.41 Laboratory Analyte Result (Observation) |
   37.42 Observation |
   37.43 Observation Panel |
   37.44 OperationOutcome |
   37.45 Organization |
   37.46 Patient |
   37.47 Practitioner |
   37.48 PractitionerRole |
   37.49 Procedure |
   37.50 Questionnaire |
   37.51 QuestionnaireResponse |
   37.52 RelatedPerson |
   37.53 ServiceRequest |
   37.54 Specimen |
   37.55 Task |
   37.56 Therapeutic Implication (Observation) |
   37.57 Variant (Observation) |
   37.58 Visit |
   37.59 Attachment |
   37.60 CodeableReference |
   37.61 Correlation Identifier |
   37.62 Genomics Pedigree Number |
   37.63 GS1 Global Service Relation Number (GSRN) |
   37.64 GS1 Serial Shipping Container Code (SSCC) |
   37.65 GS1 Service Relation Instance Number (SRIN) |
   37.66 Hospital Provider Spell Identifier |
   37.67 Medical Record Number |
   37.68 NHS Identifier |
   37.69 Order Group Number |
   37.70 Order Identifier |
   37.71 Organisation Code |
   37.72 Organisation Site Identifier |
   37.73 Practitioner Identifier |
   37.74 Report Identifier |
   37.75 Shipment Tracking Number |
   37.76 Specimen Accession Number |
   37.77 Visit Number |
   37.78 ExtCodeableReference |
   37.79 Admission Method |
   37.80 Admission Source |
   37.81 Discharge Destination |
   37.82 Discharge Disposition |
   37.83 DocumentEntry Class |
   37.84 DocumentEntry mimeType |
   37.85 DocumentEntry Type |
   37.86 Ethnicity |
   37.87 Facility Type |
   37.88 Genomic Cancer Test Directory |
   37.89 Genomic Clinical Indication Codes |
   37.90 Genomic Disorder Carrier |
   37.91 Genomic Finding |
   37.92 Genomic Finding Detected |
   37.93 Genomic Rare and Inherited Disease Test Directory |
   37.94 Genomic Test Codes |
   37.95 Genomic Test Outcome Codes |
   37.96 NW IdentifierType |
   37.97 Order Category |
   37.98 Organisation Cheshire and Merseyside ICS (QYG) NHS Trusts |
   37.99 Organisation Greater Manchester ICS (QOP) NHS Trusts |
   37.100 Organisation Lancashire and South Cumbria ICS (QE1) NHS Trusts |
   37.101 Organisation North West Region NHS Trusts |
   37.102 Patient Encounter Trigger |
   37.103 Patient Identity Trigger |
   37.104 Practitioner Identifiers |
   37.105 Pregnancy |
   37.106 Request Priority |
   37.107 Service |
   37.108 Specialty |
   37.109 Specimen Body Site |
   37.110 Specimen Tracking Events |
   37.111 Specimen Type |
   37.112 UK National Health Identifiers |
   37.113 Yes/No |
   37.114 Yes/No/Unknown |
   37.115 iGene Codes |
   37.116 iGene Sample Sub Type |
   37.117 iGene Test Codes |
   37.118 MFT EPIC Question Ids |
   37.119 NHS England Genomic Clinical Indication Code |
   37.120 NHS England Genomic Test Code |
   37.121 NHS England Genomic Test Outcome Code |
   37.122 NW GMSA Codes |
   37.123 UK National Health Identifiers |
   37.124 UK Professional License |
   37.125 GMC Number |
   37.126 GMP Number |
   37.127 NHS Number |
   37.128 ODS Code |
   37.129 ODS Site Code |
   37.130 LOINC to SNOMED UK edition |
   37.131 Sample Body Site (SNOMED) to iGene Specimen Sub Type |
   37.132 Sample Type (SNOMED) to iGene Specimen Type |
   37.133 SNOMED LOINC edition to SNOMED UK edition |
   37.134 Clinical and Genomic Workflow |
   37.135 Collect Specimen - Biopsy Procedure for obtaining a specimen, part of a diagnostic pathway. Day case admission. |
   37.136 Genomic Test Order Process including order entry and transmission of the order |
   37.137 Genomic Test Report Process |
   37.138 AuditEvent Mobile Query Existing Data [PCC-44] |
   37.139 AuditEvent Placer Order Management [LAB-1] V2/FHIR/V2 Order |
   37.140 Bundle 'Event Message' - Patient Update |
   37.141 Bundle 'Message' - Genomics Order Reply |
   37.142 Bundle 'Message' - Genomics Order Reply Acknowledgement |
   37.143 Bundle 'Transaction' - Genomics Order Asynchronous Message Reply Acknowledgement |
   37.144 Bundle - Conditions for a Patient QEDm |
   37.145 Bundle - Form Search Results SDC |
   37.146 Bundle - Genomic Diagnostic Implication for a Patient QEDm |
   37.147 Bundle - Genomic Variant for a Patient QEDm |
   37.148 Bundle - Genomic Variant Gene = NTHL1 QEDm |
   37.149 Bundle - Patient Search Results by Medical Record Number PDQ |
   37.150 Bundle - Patient Search Results by NHS Number PDQ |
   37.151 Condition - Carcinoma |
   37.152 Condition - Lynch Syndrome |
   37.153 Consanguinity (type=CE) |
   37.154 FamilyMemberHistory - Ricky LEEDS |
   37.155 FamilyMemberHistory - Sarah-Jane Nottingham |
   37.156 FHIR RESTful POST ServiceRequest |
   37.157 Genomic Order Entry Optional Questions |
   37.158 Genomic Report BRCA1 Variant Example |
   37.159 Genomic Report Ovarian Carcinoma Diagnostic Implication Example |
   37.160 Genomic Study (Panel) - Cystic Fibrosis |
   37.161 Genomic Study (Panel) - Lynch Syndrome |
   37.162 Laboratory Analyte Result BCRABL Invalid Example |
   37.163 Laboratory Analyte Result BCRABL Valid Example |
   37.164 MCV - Mean corpuscular volume |
   37.165 Message Header - Genomic Order Reply fatal |
   37.166 Message Header - Genomic Order Reply fatal Acknowledgement |
   37.167 Message Header - Genomic Order Reply Transient |
   37.168 Message Header - Genomic Report |
   37.169 Message Header - Patient |
   37.170 Observation - Lynch Syndrome Mutation Finding |
   37.171 Order Tracking Number (type=ST) |
   37.172 Organization MANCHESTER UNIVERSITY NHS FOUNDATION TRUST |
   37.173 Organization North West GMSA |
   37.174 Output from a FHIR Validation |
   37.175 Parameters Expansion Profile |
   37.176 Patient - Birmingham |
   37.177 Patient - Bolton |
   37.178 Patient - Congleton |
   37.179 Patient - Fetus London |
   37.180 Patient - Lancaster |
   37.181 Patient - London |
   37.182 Patient - Ned Liverpool NHS Number: 9737383206 |
   37.183 Patient - Northwich |
   37.184 Patient - Nottingham |
   37.185 Patient - Rob Leeds NHS Number: 9737383222 |
   37.186 Patient - Sansa Manchester NHS Number: 9737383192 |
   37.187 Patient - Warrington |
   37.188 Patient - Wrexham |
   37.189 PractitionerRole Result INTERPRETER |
   37.190 Pregnancy Expected Delivery Date (type=DT) |
   37.191 Procedure - Liver Biopsy |
   37.192 RelatedPerson Birmingham-Lancaster |
   37.193 RelatedPerson Birmingham-London |
   37.194 RelatedPerson Lancaster-London |
   37.195 RelatedPerson London-Lancaster |
   37.196 RelatedPerson Mother Cersei London |
   37.197 RelatedPerson Wrexham-Lancaster |
   37.198 RelatedPerson Wrexham-London |
   37.199 Task Genomic Test Completed |
   37.200 Task Genomic Test Requested |
   37.201 Binary Genomic Record of Discussion Example |
   37.202 Bundle 'Message' - Genomics Order Reply |
   37.203 Bundle 'Message' - Genomics Order with Attachment |
   37.204 Bundle 'Message' - Genomics Order with Coded Entries |
   37.205 Bundle 'SearchSet' - Genomics Order |
   37.206 Document Reference Laboratory Order |
   37.207 Encounter 'episode/stay' Example |
   37.208 Message Header - Genomic Order |
   37.209 Message Header - Genomic Order Reply ok |
   37.210 Patient - OctaviaCHISLETT NHS Number: 9449305552 |
   37.211 PractitionerRole C3456789 Example |
   37.212 ServiceRequest Attachment Example |
   37.213 ServiceRequest Coded Entries Example |
   37.214 Specimen Example |
   37.215 Binary Genomic Report Example |
   37.216 Bundle 'Message' - Genomics Report |
   37.217 Diagnostic Report Example. |
   37.218 Document Reference Laboratory Report |
   37.219 Message Header - Genomic Report |
   37.220 DiagnosticImplication - Cystic Fibrosis Carrier |
   37.221 DiagnosticImplication - Lynch Syndrome |
   37.222 Genomic Study - Cystic Fibrosis |
   37.223 Genomic Study - Lynch Syndrome |
   37.224 Variant - CFTR |
   37.225 Variant - NTHL1 |
   37.226 748683741 |
   37.227 Bundle `Document` - Genetic Report |
   37.228 Composition - Genomics Report Octavia CHISLETT |
   37.229 EPIC-OBR-1 Example |
   37.230 EPIC-OBX-10 Example |
   37.231 EPIC-OBX-11 Example |
   37.232 EPIC-OBX-2 Example |
   37.233 EPIC-OBX-4 Example |
   37.234 EPIC-OBX-6 Example |
   37.235 EPIC-OBX-7 Example |
   37.236 EPIC-OBX-8 Example |
   37.237 Genomic Referral Category |
   37.238 High infection risk sample |
   37.239 Informed Consent |
   37.240 OBX Pregnancy |
   37.241 Supervising Clinician |
   37.242 Bundle-Bundle-NonWGSTestOrderForm-Reanalysis-Example |
   37.243 Bundle-NonWGSTestOrderForm-CancerSolidTumor-Example |
   37.244 Bundle-NonWGSTestOrderForm-FetalScenario-Example |
   37.245 NRL Genomic Report for Cersei LONDON (Test NHS Number 9737383230). Original order electronic from EPIC system |
   37.246 NRL Genomic Report for Tommen BIRMINGHAM (Test NHS Number 9737383249). Original order not electronic |
   37.247 837d78a0-30cd-478c-83a8-f83d16fc4443 |