Logica COVID-19 FHIR Profile Library IG
0.13.1 - ci-build
Logica COVID-19 FHIR Profile Library IG
0.13.1 - ci-build
Logica COVID-19 FHIR Profile Library IG - Local Development build (v0.13.1). See the Directory of published versions
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<ValueSet xmlns="http://hl7.org/fhir">
<id value="covid91-underlying-hemoglobinopathy-condition-value-set"/>
<text>
<status value="generated"/>
<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://browser.ihtsdotools.org/?perspective=full&conceptId1=68913001">68913001</a></td><td>Alpha thalassemia (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=36351005">36351005</a></td><td>Antithrombin III deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=306058006">306058006</a></td><td>Aplastic anemia (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=707147002">707147002</a></td><td>Asplenia (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=65959000">65959000</a></td><td>Beta thalassemia (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=64779008">64779008</a></td><td>Blood coagulation disorder (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=715559004">715559004</a></td><td>Combined deficiency of factor V and factor VIII (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=767712006">767712006</a></td><td>Factor IX deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=4320005">4320005</a></td><td>Factor V deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=307091009">307091009</a></td><td>Factor V Leiden mutation (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=37193007">37193007</a></td><td>Factor VII deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=76642003">76642003</a></td><td>Factor X deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=767713001">767713001</a></td><td>Factor XI deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=359727008">359727008</a></td><td>Fibrinogen deficiency (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=90935002">90935002</a></td><td>Hemophilia (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=41788008">41788008</a></td><td>Hereditary factor IX deficiency disease (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=28293008">28293008</a></td><td>Hereditary factor VIII deficiency disease (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=49762007">49762007</a></td><td>Hereditary factor XI deficiency disease (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=84828003">84828003</a></td><td>Leukopenia (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=109995007">109995007</a></td><td>Myelodysplastic syndrome (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=165517008">165517008</a></td><td>Neutropenia (finding)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=127034005">127034005</a></td><td>Pancytopenia (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=109992005">109992005</a></td><td>Polycythemia vera (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=76407009">76407009</a></td><td>Protein C deficiency disease (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=1563006">1563006</a></td><td>Protein S deficiency disease (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=440989002">440989002</a></td><td>Prothrombin G20210A mutation (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=127041004">127041004</a></td><td>Sickle cell-beta-thalassemia (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=127040003">127040003</a></td><td>Sickle cell-hemoglobin SS disease (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=417357006">417357006</a></td><td>Sickling disorder due to hemoglobin S (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=302215000">302215000</a></td><td>Thrombocytopenic disorder (disorder)</td></tr><tr><td><a href="http://browser.ihtsdotools.org/?perspective=full&conceptId1=128105004">128105004</a></td><td>von Willebrand disorder (disorder)</td></tr></table></li></ul></div>
</text>
<url
value="http://fhir.logicahealth.org/covid19/ValueSet/covid91-underlying-hemoglobinopathy-condition-value-set"/>
<version value="0.13.1"/>
<name value="COVID19UnderlyingHemoglobinopathyConditionVS"/>
<title value="COVID-19 hemoglobinopathy underlying condition reference set"/>
<status value="active"/>
<date value="2021-08-09T20:08:14+00:00"/>
<publisher value="Logica"/>
<contact>
<name value="Logica"/>
<telecom>
<system value="url"/>
<value value="https://www.logicahealth.org/"/>
</telecom>
</contact>
<description
value="A set of codes that describe underlying hemoglobinopathy conditions for COVID19"/>
<compose>
<include>
<system value="http://snomed.info/sct"/>
<concept>
<code value="68913001"/>
<display value="Alpha thalassemia (disorder)"/>
</concept>
<concept>
<code value="36351005"/>
<display value="Antithrombin III deficiency (disorder)"/>
</concept>
<concept>
<code value="306058006"/>
<display value="Aplastic anemia (disorder)"/>
</concept>
<concept>
<code value="707147002"/>
<display value="Asplenia (disorder)"/>
</concept>
<concept>
<code value="65959000"/>
<display value="Beta thalassemia (disorder)"/>
</concept>
<concept>
<code value="64779008"/>
<display value="Blood coagulation disorder (disorder)"/>
</concept>
<concept>
<code value="715559004"/>
<display
value="Combined deficiency of factor V and factor VIII (disorder)"/>
</concept>
<concept>
<code value="767712006"/>
<display value="Factor IX deficiency (disorder)"/>
</concept>
<concept>
<code value="4320005"/>
<display value="Factor V deficiency (disorder)"/>
</concept>
<concept>
<code value="307091009"/>
<display value="Factor V Leiden mutation (disorder)"/>
</concept>
<concept>
<code value="37193007"/>
<display value="Factor VII deficiency (disorder)"/>
</concept>
<concept>
<code value="76642003"/>
<display value="Factor X deficiency (disorder)"/>
</concept>
<concept>
<code value="767713001"/>
<display value="Factor XI deficiency (disorder)"/>
</concept>
<concept>
<code value="359727008"/>
<display value="Fibrinogen deficiency (disorder)"/>
</concept>
<concept>
<code value="90935002"/>
<display value="Hemophilia (disorder)"/>
</concept>
<concept>
<code value="41788008"/>
<display value="Hereditary factor IX deficiency disease (disorder)"/>
</concept>
<concept>
<code value="28293008"/>
<display value="Hereditary factor VIII deficiency disease (disorder)"/>
</concept>
<concept>
<code value="49762007"/>
<display value="Hereditary factor XI deficiency disease (disorder)"/>
</concept>
<concept>
<code value="84828003"/>
<display value="Leukopenia (disorder)"/>
</concept>
<concept>
<code value="109995007"/>
<display value="Myelodysplastic syndrome (disorder)"/>
</concept>
<concept>
<code value="165517008"/>
<display value="Neutropenia (finding)"/>
</concept>
<concept>
<code value="127034005"/>
<display value="Pancytopenia (disorder)"/>
</concept>
<concept>
<code value="109992005"/>
<display value="Polycythemia vera (disorder)"/>
</concept>
<concept>
<code value="76407009"/>
<display value="Protein C deficiency disease (disorder)"/>
</concept>
<concept>
<code value="1563006"/>
<display value="Protein S deficiency disease (disorder)"/>
</concept>
<concept>
<code value="440989002"/>
<display value="Prothrombin G20210A mutation (disorder)"/>
</concept>
<concept>
<code value="127041004"/>
<display value="Sickle cell-beta-thalassemia (disorder)"/>
</concept>
<concept>
<code value="127040003"/>
<display value="Sickle cell-hemoglobin SS disease (disorder)"/>
</concept>
<concept>
<code value="417357006"/>
<display value="Sickling disorder due to hemoglobin S (disorder)"/>
</concept>
<concept>
<code value="302215000"/>
<display value="Thrombocytopenic disorder (disorder)"/>
</concept>
<concept>
<code value="128105004"/>
<display value="von Willebrand disorder (disorder)"/>
</concept>
</include>
</compose>
</ValueSet>