|   0 Table of Contents | 
|    1 Home | 
|    2 Laboratory Testing Workflow (LTW) | 
|    3 Patient Administration (PAM) | 
|    4 Healthcare Provider Directory (HPD) | 
|    5 Health Information Exchange (HIE) | 
|    6 Placer Order Management [LAB-1] | 
|    7 Filler Order Management [LAB-2] | 
|    8 Order Results Management [LAB-3] | 
|    9 Work Order Management [LAB-4] | 
|    10 Test Results Management [LAB-5] | 
|    11 Query Existing Data [QEDm] | 
|    12 Mobile Access to Health Documents [MHD] | 
|    13 Overview | 
|    14 HL7 v2 Artefacts | 
|    15 Architecture | 
|    16 Testing | 
|    17 Support | 
|    18 Authorisation (OAuth2) | 
|    19 Deployment | 
|    20 OAuth2 | 
|    21 Workflow Options | 
|    22 Identifiers and Codes | 
|    23 Domain Archetypes Introduction | 
|    24 Care Services Discovery | 
|    25 Artifacts Summary | 
|     25.1 Automation Manager | 
|     25.2 Clinical Document | 
|     25.3 Intermediary | 
|     25.4 Order Filler | 
|     25.5 Order Placer | 
|     25.6 Order Result Tracker | 
|     25.7 Patient Identity Source | 
|     25.8 Provider Information Source | 
|     25.9 CapabilityStatement for NW GMSA Clinical Data Repository | 
|     25.10 CapabilityStatement for NW GMSA Regional Integration Engine for Genomics | 
|     25.11 Process Message | 
|     25.12 Message Definition - Laboratory Order | 
|     25.13 Message Definition - Patient Encounter | 
|     25.14 Message Definition - Patient Identity | 
|     25.15 Message Definition - Unsolicited Observation | 
|     25.16 assigner | 
|     25.17 CBC panel - Blood by Automated count | 
|     25.18 Comprehensive metabolic 2000 panel - Serum or Plasma | 
|     25.19 Master HL7 genetic variant reporting panel | 
|     25.20 North West Genomics Test Order | 
|     25.21 North West Genomics Test Order Future | 
|     25.22 North West Genomics Test Report | 
|     25.23 Pedigree | 
|     25.24 Binary | 
|     25.25 Composition | 
|     25.26 Composition Genomic Report | 
|     25.27 Condition | 
|     25.28 Diagnostic Report | 
|     25.29 DocumentReference | 
|     25.30 Encounter | 
|     25.31 MessageHeader | 
|     25.32 Observation | 
|     25.33 Observation Diagnostic Implication | 
|     25.34 Observation Genotype | 
|     25.35 Observation Panel | 
|     25.36 Observation Therapeutic Implication | 
|     25.37 Observation Variant | 
|     25.38 OperationOutcome | 
|     25.39 Organization | 
|     25.40 Patient | 
|     25.41 Practitioner | 
|     25.42 PractitionerRole | 
|     25.43 Procedure Genomic Study | 
|     25.44 Questionnaire | 
|     25.45 QuestionnaireResponse | 
|     25.46 ServiceRequest | 
|     25.47 Specimen | 
|     25.48 Task | 
|     25.49 Accession Number | 
|     25.50 Attachment | 
|     25.51 CodeableReference | 
|     25.52 Correlation Identifier | 
|     25.53 Filler Order Number | 
|     25.54 Genomics Pedigree Number | 
|     25.55 Hospital Provider Spell Identifier | 
|     25.56 Medical Record Number | 
|     25.57 NHS Number | 
|     25.58 Organisation Code | 
|     25.59 Organisation Site Identifier | 
|     25.60 Placer Group Number | 
|     25.61 Placer Order Number | 
|     25.62 Practitioner Identifier | 
|     25.63 Report Number | 
|     25.64 Shipment Tracking Number | 
|     25.65 DiagnosticReport procedure | 
|     25.66 ExtCodeableReference | 
|     25.67 Admission Method | 
|     25.68 Admission Source | 
|     25.69 Discharge Destination | 
|     25.70 Discharge Disposition | 
|     25.71 DocumentEntry Class | 
|     25.72 DocumentEntry mimeType | 
|     25.73 DocumentEntry Type | 
|     25.74 Ethnicity | 
|     25.75 Facility Type | 
|     25.76 Genomic Cancer Test Directory | 
|     25.77 Genomic Clinical Indication Codes | 
|     25.78 Genomic Disorder Carrier | 
|     25.79 Genomic Finding | 
|     25.80 Genomic Finding Detected | 
|     25.81 Genomic Rare and Inherited Disease Test Directory | 
|     25.82 Genomic Test Codes | 
|     25.83 Genomic Test Outcome Codes | 
|     25.84 NW IdentifierType | 
|     25.85 Order Category | 
|     25.86 Patient Encounter Trigger | 
|     25.87 Patient Identity Trigger | 
|     25.88 Practitioner Identifiers | 
|     25.89 Request Priority | 
|     25.90 Service | 
|     25.91 Specialty | 
|     25.92 Specimen Type | 
|     25.93 Yes/No | 
|     25.94 Yes/No/Unknown | 
|     25.95 MFT EPIC Question Ids | 
|     25.96 NHS England Genomic Clinical Indication Code | 
|     25.97 NHS England Genomic Test Code | 
|     25.98 NHS England Genomic Test Outcome Code | 
|     25.99 NW GMSA Codes | 
|     25.100 UK Professional License | 
|     25.101 GMC Number | 
|     25.102 GMP Number | 
|     25.103 NHS Number | 
|     25.104 ODS Code | 
|     25.105 ODS Site Code | 
|     25.106 LOINC to SNOMED UK edition | 
|     25.107 SNOMED LOINC edition to SNOMED UK edition | 
|     25.108 Clinical and Genomic Workflow | 
|     25.109 Collect Specimen - Biopsy Procedure for obtaining a specimen, part of a diagnostic pathway. Day case admission. | 
|     25.110 Genomic Test Order Process including order entry and transmission of the order | 
|     25.111 Genomic Test Report Process | 
|     25.112 Bundle 'Event Message' - Patient Update | 
|     25.113 Bundle 'Message' - Genomics Order Reply | 
|     25.114 Bundle 'Message' - Genomics Order Reply Acknowledgement | 
|     25.115 Bundle 'Transaction' - Genomics Order Asynchronous Message Reply Acknowledgement | 
|     25.116 Bundle - Conditions for a Patient QEDm | 
|     25.117 Bundle - Form Search Results SDC | 
|     25.118 Bundle - Genomic Diagnostic Implication for a Patient QEDm | 
|     25.119 Bundle - Genomic Variant for a Patient QEDm | 
|     25.120 Bundle - Genomic Variant Gene =  NTHL1 QEDm | 
|     25.121 Bundle - Patient Search Results by Medical Record Number PDQ | 
|     25.122 Bundle - Patient Search Results by NHS Number PDQ | 
|     25.123 Condition - Carcinoma | 
|     25.124 Condition - Lynch Syndrome | 
|     25.125 Consanguinity (type=CE) | 
|     25.126 FamilyMemberHistory - Ricky LEEDS | 
|     25.127 FamilyMemberHistory - Sarah-Jane Nottingham | 
|     25.128 Genomic Order Entry Optional Questions | 
|     25.129 Genomic Report BRCA1 Variant Example | 
|     25.130 Genomic Report Ovarian Carcinoma Diagnostic Implication Example | 
|     25.131 MCV - Mean corpuscular volume | 
|     25.132 Message Header - Genomic Order Reply fatal | 
|     25.133 Message Header - Genomic Order Reply fatal Acknowledgement | 
|     25.134 Message Header - Genomic Order Reply Transient | 
|     25.135 Message Header - Genomic Report | 
|     25.136 Message Header - Patient | 
|     25.137 Observation - Lynch Syndrome Mutation Finding | 
|     25.138 Order Tracking Number (type=ST) | 
|     25.139 Organization MANCHESTER UNIVERSITY NHS FOUNDATION TRUST | 
|     25.140 Organization North West GMSA | 
|     25.141 Output from a FHIR Validation | 
|     25.142 Parameters Expansion Profile | 
|     25.143 Patient - Liam Manchester NHS Number: 9012345678 | 
|     25.144 Patient - Paul Liverpool NHS Number: 9876543210 | 
|     25.145 Patient - Ricky Leeds NHS Number: 9321087654 | 
|     25.146 PractitionerRole Result INTERPRETER | 
|     25.147 Pregnancy Expected Delivery Date (type=DT) | 
|     25.148 Procedure - Liver Biopsy | 
|     25.149 Task Genomic Test Completed | 
|     25.150 Task Genomic Test Requested | 
|     25.151 Binary Genomic Record of Discussion Example | 
|     25.152 Bundle 'Message' - Genomics Order Reply | 
|     25.153 Bundle 'Message' - Genomics Order with Attachment | 
|     25.154 Bundle 'Message' - Genomics Order with Coded Entries | 
|     25.155 Bundle 'SearchSet' - Genomics Order | 
|     25.156 Document Reference Laboratory Order | 
|     25.157 Encounter 'episode/stay' Example | 
|     25.158 Message Header - Genomic Order | 
|     25.159 Message Header - Genomic Order Reply ok | 
|     25.160 Patient - OctaviaCHISLETT NHS Number: 9449305552 | 
|     25.161 PractitionerRole C3456789 Example | 
|     25.162 ServiceRequest Attachment Example | 
|     25.163 ServiceRequest Coded Entries Example | 
|     25.164 Specimen Example | 
|     25.165 Binary Genomic Report Example | 
|     25.166 Bundle 'Message' - Genomics Report | 
|     25.167 Diagnostic Report Example. | 
|     25.168 Document Reference Laboratory Report | 
|     25.169 Message Header - Genomic Report | 
|     25.170 DiagnosticImplication - Cystic Fibrosis Carrier | 
|     25.171 DiagnosticImplication - Lynch Syndrome | 
|     25.172 Genomic Study - Cystic Fibrosis | 
|     25.173 Genomic Study - Lynch Syndrome | 
|     25.174 Variant - CFTR | 
|     25.175 Variant - NTHL1 | 
|     25.176 Bundle `Document` - Genetic Report | 
|     25.177 Composition - Genomics Report Octavia CHISLETT | 
|     25.178 EPIC-OBR-1 Example | 
|     25.179 EPIC-OBX-10 Example | 
|     25.180 EPIC-OBX-11 Example | 
|     25.181 EPIC-OBX-2 Example | 
|     25.182 EPIC-OBX-4 Example | 
|     25.183 EPIC-OBX-6 Example | 
|     25.184 EPIC-OBX-7 Example | 
|     25.185 EPIC-OBX-8 Example | 
|     25.186 Genomic Referral Category | 
|     25.187 High infection risk sample | 
|     25.188 Informed Consent | 
|     25.189 OBX Pregnancy | 
|     25.190 Supervising Clinician | 
|     25.191 Bundle-Bundle-NonWGSTestOrderForm-Reanalysis-Example | 
|     25.192 Bundle-NonWGSTestOrderForm-CancerSolidTumor-Example | 
|     25.193 Bundle-NonWGSTestOrderForm-FetalScenario-Example | 
|     25.194 837d78a0-30cd-478c-83a8-f83d16fc4443 |