COVID-19 FHIR Profile Library IG Informative Version
1.0.0 - Informative US

This page is part of the Logica COVID-19 FHIR Profile Library IG (v1.0.0: Informative - Informative) based on FHIR R4. This is the current published version. For a full list of available versions, see the Directory of published versions

: COVID-19 hemoglobinopathy underlying condition reference set - TTL Representation

Active as of 2022-07-25

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@prefix fhir: <http://hl7.org/fhir/> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

# - resource -------------------------------------------------------------------

 a fhir:ValueSet;
  fhir:nodeRole fhir:treeRoot;
  fhir:Resource.id [ fhir:value "covid91-underlying-hemoglobinopathy-condition-value-set"];
  fhir:DomainResource.text [
     fhir:Narrative.status [ fhir:value "generated" ];
     fhir:Narrative.div "<div xmlns=\"http://www.w3.org/1999/xhtml\"><ul><li>Include these codes as defined in <a href=\"http://www.snomed.org/\"><code>http://snomed.info/sct</code></a><table class=\"none\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td><a href=\"http://snomed.info/id/68913001\">68913001</a></td><td>Alpha thalassemia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/36351005\">36351005</a></td><td>Antithrombin III deficiency (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/306058006\">306058006</a></td><td>Aplastic anemia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/707147002\">707147002</a></td><td>Asplenia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/65959000\">65959000</a></td><td>Beta thalassemia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/64779008\">64779008</a></td><td>Blood coagulation disorder (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/715559004\">715559004</a></td><td>Combined deficiency of factor V and factor VIII (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/767712006\">767712006</a></td><td>Factor IX deficiency (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/4320005\">4320005</a></td><td>Factor V deficiency (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/307091009\">307091009</a></td><td>Factor V Leiden mutation (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/37193007\">37193007</a></td><td>Factor VII deficiency (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/76642003\">76642003</a></td><td>Factor X deficiency (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/767713001\">767713001</a></td><td>Factor XI deficiency (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/359727008\">359727008</a></td><td>Fibrinogen deficiency (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/90935002\">90935002</a></td><td>Hemophilia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/41788008\">41788008</a></td><td>Hereditary factor IX deficiency disease (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/28293008\">28293008</a></td><td>Hereditary factor VIII deficiency disease (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/49762007\">49762007</a></td><td>Hereditary factor XI deficiency disease (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/84828003\">84828003</a></td><td>Leukopenia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/109995007\">109995007</a></td><td>Myelodysplastic syndrome (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/165517008\">165517008</a></td><td>Neutropenia (finding)</td></tr><tr><td><a href=\"http://snomed.info/id/127034005\">127034005</a></td><td>Pancytopenia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/109992005\">109992005</a></td><td>Polycythemia vera (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/76407009\">76407009</a></td><td>Protein C deficiency disease (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/1563006\">1563006</a></td><td>Protein S deficiency disease (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/440989002\">440989002</a></td><td>Prothrombin G20210A mutation (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/127041004\">127041004</a></td><td>Sickle cell-beta-thalassemia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/127040003\">127040003</a></td><td>Sickle cell-hemoglobin SS disease (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/417357006\">417357006</a></td><td>Sickling disorder due to hemoglobin S (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/302215000\">302215000</a></td><td>Thrombocytopenic disorder (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/128105004\">128105004</a></td><td>von Willebrand disorder (disorder)</td></tr></table></li></ul></div>"
  ];
  fhir:ValueSet.url [ fhir:value "http://hl7.org/fhir/us/covid19library/ValueSet/covid91-underlying-hemoglobinopathy-condition-value-set"];
  fhir:ValueSet.version [ fhir:value "1.0.0"];
  fhir:ValueSet.name [ fhir:value "COVID19UnderlyingHemoglobinopathyConditionVS"];
  fhir:ValueSet.title [ fhir:value "COVID-19 hemoglobinopathy underlying condition reference set"];
  fhir:ValueSet.status [ fhir:value "active"];
  fhir:ValueSet.date [ fhir:value "2022-07-25T13:34:17+00:00"^^xsd:dateTime];
  fhir:ValueSet.publisher [ fhir:value "HL7 International - Clinical Information Modeling Initiative"];
  fhir:ValueSet.contact [
     fhir:index 0;
     fhir:ContactDetail.name [ fhir:value "HL7 International - Clinical Information Modeling Initiative" ];
     fhir:ContactDetail.telecom [
       fhir:index 0;
       fhir:ContactPoint.system [ fhir:value "url" ];
       fhir:ContactPoint.value [ fhir:value "http://hl7.org/Special/committees/cimi" ]     ]
  ], [
     fhir:index 1;
     fhir:ContactDetail.name [ fhir:value "Logica" ];
     fhir:ContactDetail.telecom [
       fhir:index 0;
       fhir:ContactPoint.system [ fhir:value "url" ];
       fhir:ContactPoint.value [ fhir:value "https://www.logicahealth.org/" ]     ]
  ], [
     fhir:index 2;
     fhir:ContactDetail.name [ fhir:value "HL7" ];
     fhir:ContactDetail.telecom [
       fhir:index 0;
       fhir:ContactPoint.system [ fhir:value "url" ];
       fhir:ContactPoint.value [ fhir:value "https://www.hl7.org" ]     ]
  ];
  fhir:ValueSet.description [ fhir:value "A set of codes that describe underlying hemoglobinopathy conditions for COVID19"];
  fhir:ValueSet.jurisdiction [
     fhir:index 0;
     fhir:CodeableConcept.coding [
       fhir:index 0;
       fhir:Coding.system [ fhir:value "urn:iso:std:iso:3166" ];
       fhir:Coding.code [ fhir:value "US" ];
       fhir:Coding.display [ fhir:value "United States of America" ]     ]
  ];
  fhir:ValueSet.copyright [ fhir:value "This value set includes content from SNOMED CT, which is copyright © 2002+ International Health Terminology Standards Development Organisation (IHTSDO), and distributed by agreement between IHTSDO and HL7. Implementer use of SNOMED CT is not covered by this agreement"];
  fhir:ValueSet.compose [
     fhir:ValueSet.compose.include [
       fhir:index 0;
       fhir:ValueSet.compose.include.system [ fhir:value "http://snomed.info/sct" ];
       fhir:ValueSet.compose.include.concept [
         fhir:index 0;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "68913001" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Alpha thalassemia (disorder)" ]       ], [
         fhir:index 1;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "36351005" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Antithrombin III deficiency (disorder)" ]       ], [
         fhir:index 2;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "306058006" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Aplastic anemia (disorder)" ]       ], [
         fhir:index 3;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "707147002" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Asplenia (disorder)" ]       ], [
         fhir:index 4;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "65959000" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Beta thalassemia (disorder)" ]       ], [
         fhir:index 5;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "64779008" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Blood coagulation disorder (disorder)" ]       ], [
         fhir:index 6;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "715559004" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Combined deficiency of factor V and factor VIII (disorder)" ]       ], [
         fhir:index 7;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "767712006" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Factor IX deficiency (disorder)" ]       ], [
         fhir:index 8;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "4320005" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Factor V deficiency (disorder)" ]       ], [
         fhir:index 9;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "307091009" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Factor V Leiden mutation (disorder)" ]       ], [
         fhir:index 10;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "37193007" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Factor VII deficiency (disorder)" ]       ], [
         fhir:index 11;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "76642003" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Factor X deficiency (disorder)" ]       ], [
         fhir:index 12;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "767713001" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Factor XI deficiency (disorder)" ]       ], [
         fhir:index 13;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "359727008" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Fibrinogen deficiency (disorder)" ]       ], [
         fhir:index 14;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "90935002" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Hemophilia (disorder)" ]       ], [
         fhir:index 15;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "41788008" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Hereditary factor IX deficiency disease (disorder)" ]       ], [
         fhir:index 16;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "28293008" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Hereditary factor VIII deficiency disease (disorder)" ]       ], [
         fhir:index 17;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "49762007" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Hereditary factor XI deficiency disease (disorder)" ]       ], [
         fhir:index 18;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "84828003" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Leukopenia (disorder)" ]       ], [
         fhir:index 19;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "109995007" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Myelodysplastic syndrome (disorder)" ]       ], [
         fhir:index 20;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "165517008" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Neutropenia (finding)" ]       ], [
         fhir:index 21;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "127034005" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Pancytopenia (disorder)" ]       ], [
         fhir:index 22;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "109992005" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Polycythemia vera (disorder)" ]       ], [
         fhir:index 23;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "76407009" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Protein C deficiency disease (disorder)" ]       ], [
         fhir:index 24;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "1563006" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Protein S deficiency disease (disorder)" ]       ], [
         fhir:index 25;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "440989002" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Prothrombin G20210A mutation (disorder)" ]       ], [
         fhir:index 26;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "127041004" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Sickle cell-beta-thalassemia (disorder)" ]       ], [
         fhir:index 27;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "127040003" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Sickle cell-hemoglobin SS disease (disorder)" ]       ], [
         fhir:index 28;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "417357006" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Sickling disorder due to hemoglobin S (disorder)" ]       ], [
         fhir:index 29;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "302215000" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "Thrombocytopenic disorder (disorder)" ]       ], [
         fhir:index 30;
         fhir:ValueSet.compose.include.concept.code [ fhir:value "128105004" ];
         fhir:ValueSet.compose.include.concept.display [ fhir:value "von Willebrand disorder (disorder)" ]       ]     ]
  ].

# - ontology header ------------------------------------------------------------

 a owl:Ontology;
  owl:imports fhir:fhir.ttl.