11{
2- "resourceType" : " ServiceRequest" ,
3- "id" : " ServiceRequest-NonWGSTestOrderForm-Example" ,
4- "extension" : [
5- {
6- "url" : " https://fhir.hl7.org.uk/StructureDefinition/Extension-UKCore-Coverage" ,
7- "valueCodeableConcept" : {
8- "coding" : [
9- {
10- "system" : " https://fhir.hl7.org.uk/CodeSystem/UKCore-FundingCategory" ,
11- "code" : " nhs-england" ,
12- "display" : " NHS England"
13- }
14- ]
15- }
16- }
17- ],
18- "status" : " active" ,
19- "intent" : " order" ,
20- "category" : [
21- {
22- "coding" : [
23- {
24- "system" : " https://fhir.hl7.org.uk/CodeSystem/UKCore-GenomeSequencingCategory" ,
25- "code" : " rare-disease-non-wgs" ,
26- "display" : " Rare Disease - Non-WGS"
27- }
28- ]
29- },
30- {
31- "coding" : [
32- {
33- "system" : " https://fhir.nhs.uk/CodeSystem/reasonfortesting-genomics" ,
34- "code" : " diagnostic" ,
35- "display" : " Diagnostic"
36- }
37- ]
38- }
39- ],
40- "priority" : " routine" ,
41- "code" : {
42- "coding" : [
43- {
44- "system" : " https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory" ,
45- "code" : " R67.2" ,
46- "display" : " Monogenic hearing loss" ,
47- "version" : " 7"
48- }
49- ]
50- },
51- "subject" : {
52- "reference" : " Patient/Patient-MeirLieberman-Example" ,
53- "identifier" : {
54- "system" : " https://fhir.nhs.uk/Id/nhs-number" ,
55- "value" : " 9449307873"
56- }
57- },
58- "authoredOn" : " 2023-08-05" ,
59- "requester" : {
60- "reference" : " PractitionerRole/PractitionerRole-GeneSmithENT-Example"
61- },
62- "supportingInfo" : [
63- {
64- "reference" : " Condition/Condition-MonogenicHearingLoss-Example"
65- },
66- {
67- "reference" : " Observation/Observation-GenomicEthnicity-Example"
68- },
69- {
70- "reference" : " Observation/Observation-NoPregnancy-Example"
71- },
72- {
73- "reference" : " Observation/Observation-NoTransplant-Example"
74- },
75- {
76- "reference" : " Observation/Observation-NoTransfusion-Example"
77- },
78- {
79- "reference" : " Condition/Condition-HearingLoss-Example"
80- }
81- ],
82- "note" : [
83- {
84- "text" : " No family history of genomic testing"
85- },
86- {
87- "text" : " Free text for diagnosis/reason for referral, relevant information including family history, phenotypic details/ HPO Terms/Patient in need of test...example"
88- }
89- ]
2+ "resourceType" : " ServiceRequest" ,
3+ "id" : " ServiceRequest-NonWGSTestOrderForm-Example" ,
4+ "extension" : [
5+ {
6+ "url" : " https://fhir.hl7.org.uk/StructureDefinition/Extension-UKCore-Coverage" ,
7+ "valueCodeableConcept" : {
8+ "coding" : [
9+ {
10+ "system" : " https://fhir.hl7.org.uk/CodeSystem/UKCore-FundingCategory" ,
11+ "code" : " nhs-england" ,
12+ "display" : " NHS England"
13+ }
14+ ]
15+ }
16+ },
17+ {
18+ "url" : " http://hl7.org/fhir/StructureDefinition/servicerequest-order-callback-phone-number" ,
19+ "valueContactPoint" : {
20+ "system" : " phone" ,
21+ "value" : " +44 20 7946 0000" ,
22+ "use" : " work"
23+ }
24+ }
25+ ],
26+ "status" : " active" ,
27+ "intent" : " order" ,
28+ "category" : [
29+ {
30+ "coding" : [
31+ {
32+ "system" : " https://fhir.hl7.org.uk/CodeSystem/UKCore-GenomeSequencingCategory" ,
33+ "code" : " rare-disease-non-wgs" ,
34+ "display" : " Rare Disease - Non-WGS"
35+ }
36+ ]
37+ },
38+ {
39+ "coding" : [
40+ {
41+ "system" : " https://fhir.nhs.uk/CodeSystem/reasonfortesting-genomics" ,
42+ "code" : " diagnostic" ,
43+ "display" : " Diagnostic"
44+ }
45+ ]
46+ }
47+ ],
48+ "priority" : " routine" ,
49+ "code" : {
50+ "coding" : [
51+ {
52+ "system" : " https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory" ,
53+ "code" : " R67.2" ,
54+ "display" : " Monogenic hearing loss" ,
55+ "version" : " 7"
56+ }
57+ ]
58+ },
59+ "subject" : {
60+ "reference" : " Patient/Patient-MeirLieberman-Example" ,
61+ "identifier" : {
62+ "system" : " https://fhir.nhs.uk/Id/nhs-number" ,
63+ "value" : " 9449307873"
64+ }
65+ },
66+ "authoredOn" : " 2023-08-05" ,
67+ "requester" : {
68+ "reference" : " PractitionerRole/PractitionerRole-GeneSmithENT-Example"
69+ },
70+ "supportingInfo" : [
71+ {
72+ "reference" : " Condition/Condition-MonogenicHearingLoss-Example"
73+ },
74+ {
75+ "reference" : " Observation/Observation-GenomicEthnicity-Example"
76+ },
77+ {
78+ "reference" : " Observation/Observation-NoPregnancy-Example"
79+ },
80+ {
81+ "reference" : " Observation/Observation-NoTransplant-Example"
82+ },
83+ {
84+ "reference" : " Observation/Observation-NoTransfusion-Example"
85+ },
86+ {
87+ "reference" : " Condition/Condition-HearingLoss-Example"
88+ }
89+ ],
90+ "note" : [
91+ {
92+ "text" : " No family history of genomic testing"
93+ },
94+ {
95+ "text" : " Free text for diagnosis/reason for referral, relevant information including family history, phenotypic details/ HPO Terms/Patient in need of test...example"
96+ }
97+ ]
9098}
0 commit comments