COVID-19 FHIR Profile Library IG Informative Version
1.0.0 - Informative
COVID-19 FHIR Profile Library IG Informative Version
1.0.0 - Informative
COVID-19 FHIR Profile Library IG Informative Version, published by HL7 International - Clinical Information Modeling Initiative. This is not an authorized publication; it is the continuous build for version 1.0.0). This version is based on the current content of https://github.com/HL7/fhir-COVID19Library-ig/ and changes regularly. See the Directory of published versions
| Active as of 2022-07-25 |
<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://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>
</text>
<url
value="http://hl7.org/fhir/us/covid19library/ValueSet/covid91-underlying-hemoglobinopathy-condition-value-set"/>
<version value="1.0.0"/>
<name value="COVID19UnderlyingHemoglobinopathyConditionVS"/>
<title value="COVID-19 hemoglobinopathy underlying condition reference set"/>
<status value="active"/>
<date value="2022-07-25T12:22:40+00:00"/>
<publisher
value="HL7 International - Clinical Information Modeling Initiative"/>
<contact>
<name value="HL7 International - Clinical Information Modeling Initiative"/>
<telecom>
<system value="url"/>
<value value="http://hl7.org/Special/committees/cimi"/>
</telecom>
</contact>
<contact>
<name value="Logica"/>
<telecom>
<system value="url"/>
<value value="https://www.logicahealth.org/"/>
</telecom>
</contact>
<contact>
<name value="HL7"/>
<telecom>
<system value="url"/>
<value value="https://www.hl7.org"/>
</telecom>
</contact>
<description
value="A set of codes that describe underlying hemoglobinopathy conditions for COVID19"/>
<jurisdiction>
<coding>
<system value="urn:iso:std:iso:3166"/>
<code value="US"/>
<display value="United States of America"/>
</coding>
</jurisdiction>
<copyright
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"/>
<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>
IG © 2021+ HL7 International - Clinical Information Modeling Initiative. Package hl7.fhir.us.covid19library#1.0.0 based on FHIR 4.0.1. Generated 2022-07-25
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