ÚNICAS Rare Diseases HL7 FHIR Implementation Guide
0.0.1 - draft
ÚNICAS Rare Diseases HL7 FHIR Implementation Guide - Local Development build (v0.0.1) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions
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"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><a name=\"Condition_UNICAS-ejemploConditionDiagnostico-00\"> </a><p class=\"res-header-id\"><b>Generated Narrative: Condition UNICAS-ejemploConditionDiagnostico-00</b></p><a name=\"UNICAS-ejemploConditionDiagnostico-00\"> </a><a name=\"hcUNICAS-ejemploConditionDiagnostico-00\"> </a><div style=\"display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%\"><p style=\"margin-bottom: 0px\"/><p style=\"margin-bottom: 0px\">Profile: <a href=\"StructureDefinition-UNICASConditionDiagnostico.html\">Condition Diagnóstico ÚNICAS</a></p></div><p><b>identifier</b>: <code>urn:regcess:0908005177</code>/id-interno-diagnostico-ejemplo-00</p><p><b>clinicalStatus</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/condition-clinical active}\">Active</span></p><p><b>category</b>: <span title=\"Codes:{http://snomed.info/sct/900000001000122104 8319008}\">diagnóstico primario</span>, <span title=\"Codes:{http://snomed.info/sct/900000001000122104 60022001}\">diagnóstico en sospecha</span></p><p><b>code</b>: <span title=\"Codes:{http://snomed.info/sct/900000001000122104 613003}, {urn:oid:2.16.724.4.21.5.29 Q99.2}, {urn:oid:2.16.724.4.21.5.22 908}, {urn:oid:2.16.724.4.21.5.31 300624}\">Síndrome X-frágil</span></p><p><b>subject</b>: Maria Puig Grau (Identifier: código de identificación personal en el Sistema Nacional de Salud/BBBBBBBBQR648597)</p><p><b>encounter</b>: Identifier: <code>urn:regcess:0908005177</code>/id-interno-interacionClinica-ejemplo-00</p><p><b>onset</b>: 2025-03-24 12:00:00+0000</p><h3>Participants</h3><table class=\"grid\"><tr><td style=\"display: none\">-</td><td><b>Actor</b></td></tr><tr><td style=\"display: none\">*</td><td>Eva Alabart (Identifier: documento nacional de identidad/0000001X)</td></tr></table><h3>Evidences</h3><table class=\"grid\"><tr><td style=\"display: none\">-</td><td><b>Concept</b></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:{http://snomed.info/sct/900000001000122104 2095221000122101}, {http://snomed.info/sct/900000001000122104 2095291000122104}\">ejemplo comentario sobre el grado de sospecha</span></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:{http://snomed.info/sct/900000001000122104 2095231000122103}, {http://snomed.info/sct/900000001000122104 31874001}\">ejemplo comentario sobre el criterio de diagnóstico clínico</span></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:{http://snomed.info/sct/900000001000122104 2095241000122106}, {http://snomed.info/sct/900000001000122104 64100000}\">ejemplo comentario sobre el criterio de prueba genética</span></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:{http://snomed.info/sct/900000001000122104 criterio de prueba bioquímica}, {http://snomed.info/sct/900000001000122104 64100000}\">ejemplo comentario sobre el criterio de prueba bioquímica</span></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:{http://snomed.info/sct/900000001000122104 2095271000122100}, {http://snomed.info/sct/900000001000122104 64100000}\">ejemplo comentario sobre el criterio de prueba hematológica</span></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:{http://snomed.info/sct/900000001000122104 2095261000122105}, {http://snomed.info/sct/900000001000122104 64100000}\">ejemplo comentario sobre el criterio de prueba inmunológica</span></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:{http://snomed.info/sct/900000001000122104 2095281000122102}, {http://snomed.info/sct/900000001000122104 64100000}\">ejemplo comentario sobre el criterio de prueba de imagen</span></td></tr></table><p><b>note</b>: </p><blockquote><div><p>ejemplo comentario general sobre el diagnóstico</p>\n</div></blockquote></div>"
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"display" : "síndrome del cromosoma X frágil"
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{
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"code" : "300624",
"display" : "Fragile X syndrome"
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"text" : "Síndrome X-frágil"
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"code" : "64100000",
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