COVID-19 FHIR Profile Library IG
0.14.0 - Informative Ballot
COVID-19 FHIR Profile Library IG
0.14.0 - Informative Ballot
This page is part of the Logica COVID-19 FHIR Profile Library IG (v0.14.0: Drafts Ballot 2) based on FHIR R4. The current version which supercedes this version is 1.0.0. For a full list of available versions, see the Directory of published versions 
<ValueSet xmlns="http://hl7.org/fhir">
<id value="covid19-underlying-neurolgic-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/26929004">26929004</a></td><td>Alzheimer's disease (disorder)</td></tr><tr><td><a href="http://snomed.info/id/86044005">86044005</a></td><td>Amyotrophic lateral sclerosis (disorder)</td></tr><tr><td><a href="http://snomed.info/id/89369001">89369001</a></td><td>Anencephalus (disorder)</td></tr><tr><td><a href="http://snomed.info/id/23560001">23560001</a></td><td>Asperger's disorder (disorder)</td></tr><tr><td><a href="http://snomed.info/id/406506008">406506008</a></td><td>Attention deficit hyperactivity disorder (disorder)</td></tr><tr><td><a href="http://snomed.info/id/35253001">35253001</a></td><td>Attention deficit hyperactivity disorder, predominantly inattentive type (disorder)</td></tr><tr><td><a href="http://snomed.info/id/408856003">408856003</a></td><td>Autistic disorder (disorder)</td></tr><tr><td><a href="http://snomed.info/id/387732009">387732009</a></td><td>Becker muscular dystrophy (disorder)</td></tr><tr><td><a href="http://snomed.info/id/230724001">230724001</a></td><td>Cerebral amyloid angiopathy (disorder)</td></tr><tr><td><a href="http://snomed.info/id/390936003">390936003</a></td><td>Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)</td></tr><tr><td><a href="http://snomed.info/id/128188000">128188000</a></td><td>Cerebral palsy (disorder)</td></tr><tr><td><a href="http://snomed.info/id/51500006">51500006</a></td><td>Complete trisomy 18 syndrome (disorder)</td></tr><tr><td><a href="http://snomed.info/id/41040004">41040004</a></td><td>Complete trisomy 21 syndrome (disorder)</td></tr><tr><td><a href="http://snomed.info/id/111501005">111501005</a></td><td>Congenital hereditary muscular dystrophy (disorder)</td></tr><tr><td><a href="http://snomed.info/id/32219008">32219008</a></td><td>Craniorachischisis (disorder)</td></tr><tr><td><a href="http://snomed.info/id/67434000">67434000</a></td><td>Cytochrome-c oxidase deficiency (disorder)</td></tr><tr><td><a href="http://snomed.info/id/124165006">124165006</a></td><td>Deficiency of succinate dehydrogenase (disorder)</td></tr><tr><td><a href="http://snomed.info/id/281004">281004</a></td><td>Dementia associated with alcoholism (disorder)</td></tr><tr><td><a href="http://snomed.info/id/52448006">52448006</a></td><td>Dementia (disorder)</td></tr><tr><td><a href="http://snomed.info/id/237995002">237995002</a></td><td>Depletion of mitochondrial deoxyribonucleic acid (disorder)</td></tr><tr><td><a href="http://snomed.info/id/248290002">248290002</a></td><td>Developmental delay (disorder)</td></tr><tr><td><a href="http://snomed.info/id/76670001">76670001</a></td><td>Duchenne muscular dystrophy (disorder)</td></tr><tr><td><a href="http://snomed.info/id/111508004">111508004</a></td><td>Emery-Dreifuss muscular dystrophy (disorder)</td></tr><tr><td><a href="http://snomed.info/id/55999004">55999004</a></td><td>Encephalocele (disorder)</td></tr><tr><td><a href="http://snomed.info/id/84757009">84757009</a></td><td>Epilepsy (disorder)</td></tr><tr><td><a href="http://snomed.info/id/399091004">399091004</a></td><td>Facioscapulohumeral muscular dystrophy (disorder)</td></tr><tr><td><a href="http://snomed.info/id/41497008">41497008</a></td><td>Febrile convulsion (finding)</td></tr><tr><td><a href="http://snomed.info/id/613003">613003</a></td><td>Fragile X syndrome (disorder)</td></tr><tr><td><a href="http://snomed.info/id/10394003">10394003</a></td><td>Friedreich's ataxia (disorder)</td></tr><tr><td><a href="http://snomed.info/id/230270009">230270009</a></td><td>Frontotemporal dementia (disorder)</td></tr><tr><td><a href="http://snomed.info/id/51928006">51928006</a></td><td>General paresis - neurosyphilis (disorder)</td></tr><tr><td><a href="http://snomed.info/id/88611000119100">88611000119100</a></td><td>History of traumatic brain injury (situation)</td></tr><tr><td><a href="http://snomed.info/id/386806002">386806002</a></td><td>Impaired cognition (finding)</td></tr><tr><td><a href="http://snomed.info/id/2438005">2438005</a></td><td>Iniencephaly (disorder)</td></tr><tr><td><a href="http://snomed.info/id/110359009">110359009</a></td><td>Intellectual disability (disorder)</td></tr><tr><td><a href="http://snomed.info/id/792004">792004</a></td><td>Jakob-Creutzfeldt disease (disorder)</td></tr><tr><td><a href="http://snomed.info/id/39925003">39925003</a></td><td>Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (disorder)</td></tr><tr><td><a href="http://snomed.info/id/25792000">25792000</a></td><td>Kearns-Sayre syndrome (disorder)</td></tr><tr><td><a href="http://snomed.info/id/405773007">405773007</a></td><td>Kyphoscoliosis deformity of spine (disorder)</td></tr><tr><td><a href="http://snomed.info/id/414667000">414667000</a></td><td>Meningomyelocele (disorder)</td></tr><tr><td><a href="http://snomed.info/id/47437004">47437004</a></td><td>Mental handicap (finding)</td></tr><tr><td><a href="http://snomed.info/id/718214007">718214007</a></td><td>Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder)</td></tr><tr><td><a href="http://snomed.info/id/447292006">447292006</a></td><td>Mitochondrial encephalomyopathy (disorder)</td></tr><tr><td><a href="http://snomed.info/id/56267009">56267009</a></td><td>Multi-infarct dementia (disorder)</td></tr><tr><td><a href="http://snomed.info/id/24700007">24700007</a></td><td>Multiple sclerosis (disorder)</td></tr><tr><td><a href="http://snomed.info/id/240046001">240046001</a></td><td>Muscular dystrophy with predominantly proximal limb girdle distribution (disorder)</td></tr><tr><td><a href="http://snomed.info/id/73297009">73297009</a></td><td>Muscular dystrophy (disorder)</td></tr><tr><td><a href="http://snomed.info/id/91637004">91637004</a></td><td>Myasthenia gravis (disorder)</td></tr><tr><td><a href="http://snomed.info/id/230426003">230426003</a></td><td>Myoclonic epilepsy with ragged red fibers (disorder)</td></tr><tr><td><a href="http://snomed.info/id/253098009">253098009</a></td><td>Neural tube defect (disorder)</td></tr><tr><td><a href="http://snomed.info/id/230572002">230572002</a></td><td>Neuropathy due to diabetes mellitus (disorder)</td></tr><tr><td><a href="http://snomed.info/id/386033004">386033004</a></td><td>Neuropathy (disorder)</td></tr><tr><td><a href="http://snomed.info/id/44695005">44695005</a></td><td>Paralysis (finding)</td></tr><tr><td><a href="http://snomed.info/id/29426003">29426003</a></td><td>Paralytic syndrome (disorder)</td></tr><tr><td><a href="http://snomed.info/id/32798002">32798002</a></td><td>Parkinsonism (disorder)</td></tr><tr><td><a href="http://snomed.info/id/49049000">49049000</a></td><td>Parkinson's disease (disorder)</td></tr><tr><td><a href="http://snomed.info/id/237985009">237985009</a></td><td>Pearson's syndrome (disorder)</td></tr><tr><td><a href="http://snomed.info/id/302226006">302226006</a></td><td>Peripheral nerve disease (disorder)</td></tr><tr><td><a href="http://snomed.info/id/35919005">35919005</a></td><td>Pervasive developmental disorder (disorder)</td></tr><tr><td><a href="http://snomed.info/id/5335002">5335002</a></td><td>Phosphoenolpyruvate carboxykinase deficiency (disorder)</td></tr><tr><td><a href="http://snomed.info/id/87694001">87694001</a></td><td>Pyruvate carboxylase deficiency (disorder)</td></tr><tr><td><a href="http://snomed.info/id/46683007">46683007</a></td><td>Pyruvate dehydrogenase complex deficiency (disorder)</td></tr><tr><td><a href="http://snomed.info/id/11538006">11538006</a></td><td>Quadriplegia (disorder)</td></tr><tr><td><a href="http://snomed.info/id/298382003">298382003</a></td><td>Scoliosis deformity of spine (disorder)</td></tr><tr><td><a href="http://snomed.info/id/91175000">91175000</a></td><td>Seizure (finding)</td></tr><tr><td><a href="http://snomed.info/id/128613002">128613002</a></td><td>Seizure disorder (disorder)</td></tr><tr><td><a href="http://snomed.info/id/312991009">312991009</a></td><td>Senile dementia of the Lewy body type (disorder)</td></tr><tr><td><a href="http://snomed.info/id/67531005">67531005</a></td><td>Spina bifida (disorder)</td></tr><tr><td><a href="http://snomed.info/id/47311000119103">47311000119103</a></td><td>Static encephalopathy (disorder)</td></tr><tr><td><a href="http://snomed.info/id/77956009">77956009</a></td><td>Steinert myotonic dystrophy syndrome (disorder)</td></tr><tr><td><a href="http://snomed.info/id/127295002">127295002</a></td><td>Traumatic brain injury (disorder)</td></tr><tr><td><a href="http://snomed.info/id/429998004">429998004</a></td><td>Vascular dementia (disorder)</td></tr></table></li></ul></div>
</text>
<url
value="http://hl7.org/fhir/us/covid19library/ValueSet/covid19-underlying-neurolgic-condition-value-set"/>
<version value="0.14.0"/>
<name value="COVID19UnderlyingNeuroligicConditionsVS"/>
<title value="COVID-19 neurologic underlying condition reference set"/>
<status value="active"/>
<date value="2021-12-08T02:47:19+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 conditions of a neurologic nature 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="26929004"/>
<display value="Alzheimer's disease (disorder)"/>
</concept>
<concept>
<code value="86044005"/>
<display value="Amyotrophic lateral sclerosis (disorder)"/>
</concept>
<concept>
<code value="89369001"/>
<display value="Anencephalus (disorder)"/>
</concept>
<concept>
<code value="23560001"/>
<display value="Asperger's disorder (disorder)"/>
</concept>
<concept>
<code value="406506008"/>
<display value="Attention deficit hyperactivity disorder (disorder)"/>
</concept>
<concept>
<code value="35253001"/>
<display
value="Attention deficit hyperactivity disorder, predominantly inattentive type (disorder)"/>
</concept>
<concept>
<code value="408856003"/>
<display value="Autistic disorder (disorder)"/>
</concept>
<concept>
<code value="387732009"/>
<display value="Becker muscular dystrophy (disorder)"/>
</concept>
<concept>
<code value="230724001"/>
<display value="Cerebral amyloid angiopathy (disorder)"/>
</concept>
<concept>
<code value="390936003"/>
<display
value="Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)"/>
</concept>
<concept>
<code value="128188000"/>
<display value="Cerebral palsy (disorder)"/>
</concept>
<concept>
<code value="51500006"/>
<display value="Complete trisomy 18 syndrome (disorder)"/>
</concept>
<concept>
<code value="41040004"/>
<display value="Complete trisomy 21 syndrome (disorder)"/>
</concept>
<concept>
<code value="111501005"/>
<display value="Congenital hereditary muscular dystrophy (disorder)"/>
</concept>
<concept>
<code value="32219008"/>
<display value="Craniorachischisis (disorder)"/>
</concept>
<concept>
<code value="67434000"/>
<display value="Cytochrome-c oxidase deficiency (disorder)"/>
</concept>
<concept>
<code value="124165006"/>
<display value="Deficiency of succinate dehydrogenase (disorder)"/>
</concept>
<concept>
<code value="281004"/>
<display value="Dementia associated with alcoholism (disorder)"/>
</concept>
<concept>
<code value="52448006"/>
<display value="Dementia (disorder)"/>
</concept>
<concept>
<code value="237995002"/>
<display
value="Depletion of mitochondrial deoxyribonucleic acid (disorder)"/>
</concept>
<concept>
<code value="248290002"/>
<display value="Developmental delay (disorder)"/>
</concept>
<concept>
<code value="76670001"/>
<display value="Duchenne muscular dystrophy (disorder)"/>
</concept>
<concept>
<code value="111508004"/>
<display value="Emery-Dreifuss muscular dystrophy (disorder)"/>
</concept>
<concept>
<code value="55999004"/>
<display value="Encephalocele (disorder)"/>
</concept>
<concept>
<code value="84757009"/>
<display value="Epilepsy (disorder)"/>
</concept>
<concept>
<code value="399091004"/>
<display value="Facioscapulohumeral muscular dystrophy (disorder)"/>
</concept>
<concept>
<code value="41497008"/>
<display value="Febrile convulsion (finding)"/>
</concept>
<concept>
<code value="613003"/>
<display value="Fragile X syndrome (disorder)"/>
</concept>
<concept>
<code value="10394003"/>
<display value="Friedreich's ataxia (disorder)"/>
</concept>
<concept>
<code value="230270009"/>
<display value="Frontotemporal dementia (disorder)"/>
</concept>
<concept>
<code value="51928006"/>
<display value="General paresis - neurosyphilis (disorder)"/>
</concept>
<concept>
<code value="88611000119100"/>
<display value="History of traumatic brain injury (situation)"/>
</concept>
<concept>
<code value="386806002"/>
<display value="Impaired cognition (finding)"/>
</concept>
<concept>
<code value="2438005"/>
<display value="Iniencephaly (disorder)"/>
</concept>
<concept>
<code value="110359009"/>
<display value="Intellectual disability (disorder)"/>
</concept>
<concept>
<code value="792004"/>
<display value="Jakob-Creutzfeldt disease (disorder)"/>
</concept>
<concept>
<code value="39925003"/>
<display
value="Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (disorder)"/>
</concept>
<concept>
<code value="25792000"/>
<display value="Kearns-Sayre syndrome (disorder)"/>
</concept>
<concept>
<code value="405773007"/>
<display value="Kyphoscoliosis deformity of spine (disorder)"/>
</concept>
<concept>
<code value="414667000"/>
<display value="Meningomyelocele (disorder)"/>
</concept>
<concept>
<code value="47437004"/>
<display value="Mental handicap (finding)"/>
</concept>
<concept>
<code value="718214007"/>
<display
value="Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder)"/>
</concept>
<concept>
<code value="447292006"/>
<display value="Mitochondrial encephalomyopathy (disorder)"/>
</concept>
<concept>
<code value="56267009"/>
<display value="Multi-infarct dementia (disorder)"/>
</concept>
<concept>
<code value="24700007"/>
<display value="Multiple sclerosis (disorder)"/>
</concept>
<concept>
<code value="240046001"/>
<display
value="Muscular dystrophy with predominantly proximal limb girdle distribution (disorder)"/>
</concept>
<concept>
<code value="73297009"/>
<display value="Muscular dystrophy (disorder)"/>
</concept>
<concept>
<code value="91637004"/>
<display value="Myasthenia gravis (disorder)"/>
</concept>
<concept>
<code value="230426003"/>
<display value="Myoclonic epilepsy with ragged red fibers (disorder)"/>
</concept>
<concept>
<code value="253098009"/>
<display value="Neural tube defect (disorder)"/>
</concept>
<concept>
<code value="230572002"/>
<display value="Neuropathy due to diabetes mellitus (disorder)"/>
</concept>
<concept>
<code value="386033004"/>
<display value="Neuropathy (disorder)"/>
</concept>
<concept>
<code value="44695005"/>
<display value="Paralysis (finding)"/>
</concept>
<concept>
<code value="29426003"/>
<display value="Paralytic syndrome (disorder)"/>
</concept>
<concept>
<code value="32798002"/>
<display value="Parkinsonism (disorder)"/>
</concept>
<concept>
<code value="49049000"/>
<display value="Parkinson's disease (disorder)"/>
</concept>
<concept>
<code value="237985009"/>
<display value="Pearson's syndrome (disorder)"/>
</concept>
<concept>
<code value="302226006"/>
<display value="Peripheral nerve disease (disorder)"/>
</concept>
<concept>
<code value="35919005"/>
<display value="Pervasive developmental disorder (disorder)"/>
</concept>
<concept>
<code value="5335002"/>
<display value="Phosphoenolpyruvate carboxykinase deficiency (disorder)"/>
</concept>
<concept>
<code value="87694001"/>
<display value="Pyruvate carboxylase deficiency (disorder)"/>
</concept>
<concept>
<code value="46683007"/>
<display value="Pyruvate dehydrogenase complex deficiency (disorder)"/>
</concept>
<concept>
<code value="11538006"/>
<display value="Quadriplegia (disorder)"/>
</concept>
<concept>
<code value="298382003"/>
<display value="Scoliosis deformity of spine (disorder)"/>
</concept>
<concept>
<code value="91175000"/>
<display value="Seizure (finding)"/>
</concept>
<concept>
<code value="128613002"/>
<display value="Seizure disorder (disorder)"/>
</concept>
<concept>
<code value="312991009"/>
<display value="Senile dementia of the Lewy body type (disorder)"/>
</concept>
<concept>
<code value="67531005"/>
<display value="Spina bifida (disorder)"/>
</concept>
<concept>
<code value="47311000119103"/>
<display value="Static encephalopathy (disorder)"/>
</concept>
<concept>
<code value="77956009"/>
<display value="Steinert myotonic dystrophy syndrome (disorder)"/>
</concept>
<concept>
<code value="127295002"/>
<display value="Traumatic brain injury (disorder)"/>
</concept>
<concept>
<code value="429998004"/>
<display value="Vascular dementia (disorder)"/>
</concept>
</include>
</compose>
</ValueSet>
IG © 2021+ HL7 International - Clinical Information Modeling Initiative. Package hl7.fhir.us.covid19library#0.14.0 based on FHIR 4.0.1. Generated 2021-12-08
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