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 |
@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 "covid19-underlying-neurolgic-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/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>"
];
fhir:ValueSet.url [ fhir:value "http://hl7.org/fhir/us/covid19library/ValueSet/covid19-underlying-neurolgic-condition-value-set"];
fhir:ValueSet.version [ fhir:value "1.0.0"];
fhir:ValueSet.name [ fhir:value "COVID19UnderlyingNeuroligicConditionsVS"];
fhir:ValueSet.title [ fhir:value "COVID-19 neurologic underlying condition reference set"];
fhir:ValueSet.status [ fhir:value "active"];
fhir:ValueSet.date [ fhir:value "2022-07-25T12:22:40+00:00"^^xsd:dateTime];
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fhir:ContactPoint.value [ fhir:value "https://www.hl7.org" ] ]
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fhir:ValueSet.description [ fhir:value "A set of codes that describe underlying conditions of a neurologic nature for COVID19."];
fhir:ValueSet.jurisdiction [
fhir:index 0;
fhir:CodeableConcept.coding [
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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"];
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fhir:index 0;
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fhir:index 0;
fhir:ValueSet.compose.include.concept.code [ fhir:value "26929004" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Alzheimer's disease (disorder)" ] ], [
fhir:index 1;
fhir:ValueSet.compose.include.concept.code [ fhir:value "86044005" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Amyotrophic lateral sclerosis (disorder)" ] ], [
fhir:index 2;
fhir:ValueSet.compose.include.concept.code [ fhir:value "89369001" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Anencephalus (disorder)" ] ], [
fhir:index 3;
fhir:ValueSet.compose.include.concept.code [ fhir:value "23560001" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Asperger's disorder (disorder)" ] ], [
fhir:index 4;
fhir:ValueSet.compose.include.concept.code [ fhir:value "406506008" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Attention deficit hyperactivity disorder (disorder)" ] ], [
fhir:index 5;
fhir:ValueSet.compose.include.concept.code [ fhir:value "35253001" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Attention deficit hyperactivity disorder, predominantly inattentive type (disorder)" ] ], [
fhir:index 6;
fhir:ValueSet.compose.include.concept.code [ fhir:value "408856003" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Autistic disorder (disorder)" ] ], [
fhir:index 7;
fhir:ValueSet.compose.include.concept.code [ fhir:value "387732009" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Becker muscular dystrophy (disorder)" ] ], [
fhir:index 8;
fhir:ValueSet.compose.include.concept.code [ fhir:value "230724001" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Cerebral amyloid angiopathy (disorder)" ] ], [
fhir:index 9;
fhir:ValueSet.compose.include.concept.code [ fhir:value "390936003" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)" ] ], [
fhir:index 10;
fhir:ValueSet.compose.include.concept.code [ fhir:value "128188000" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Cerebral palsy (disorder)" ] ], [
fhir:index 11;
fhir:ValueSet.compose.include.concept.code [ fhir:value "51500006" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Complete trisomy 18 syndrome (disorder)" ] ], [
fhir:index 12;
fhir:ValueSet.compose.include.concept.code [ fhir:value "41040004" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Complete trisomy 21 syndrome (disorder)" ] ], [
fhir:index 13;
fhir:ValueSet.compose.include.concept.code [ fhir:value "111501005" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Congenital hereditary muscular dystrophy (disorder)" ] ], [
fhir:index 14;
fhir:ValueSet.compose.include.concept.code [ fhir:value "32219008" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Craniorachischisis (disorder)" ] ], [
fhir:index 15;
fhir:ValueSet.compose.include.concept.code [ fhir:value "67434000" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Cytochrome-c oxidase deficiency (disorder)" ] ], [
fhir:index 16;
fhir:ValueSet.compose.include.concept.code [ fhir:value "124165006" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Deficiency of succinate dehydrogenase (disorder)" ] ], [
fhir:index 17;
fhir:ValueSet.compose.include.concept.code [ fhir:value "281004" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Dementia associated with alcoholism (disorder)" ] ], [
fhir:index 18;
fhir:ValueSet.compose.include.concept.code [ fhir:value "52448006" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Dementia (disorder)" ] ], [
fhir:index 19;
fhir:ValueSet.compose.include.concept.code [ fhir:value "237995002" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Depletion of mitochondrial deoxyribonucleic acid (disorder)" ] ], [
fhir:index 20;
fhir:ValueSet.compose.include.concept.code [ fhir:value "248290002" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Developmental delay (disorder)" ] ], [
fhir:index 21;
fhir:ValueSet.compose.include.concept.code [ fhir:value "76670001" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Duchenne muscular dystrophy (disorder)" ] ], [
fhir:index 22;
fhir:ValueSet.compose.include.concept.code [ fhir:value "111508004" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Emery-Dreifuss muscular dystrophy (disorder)" ] ], [
fhir:index 23;
fhir:ValueSet.compose.include.concept.code [ fhir:value "55999004" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Encephalocele (disorder)" ] ], [
fhir:index 24;
fhir:ValueSet.compose.include.concept.code [ fhir:value "84757009" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Epilepsy (disorder)" ] ], [
fhir:index 25;
fhir:ValueSet.compose.include.concept.code [ fhir:value "399091004" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Facioscapulohumeral muscular dystrophy (disorder)" ] ], [
fhir:index 26;
fhir:ValueSet.compose.include.concept.code [ fhir:value "41497008" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Febrile convulsion (finding)" ] ], [
fhir:index 27;
fhir:ValueSet.compose.include.concept.code [ fhir:value "613003" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Fragile X syndrome (disorder)" ] ], [
fhir:index 28;
fhir:ValueSet.compose.include.concept.code [ fhir:value "10394003" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Friedreich's ataxia (disorder)" ] ], [
fhir:index 29;
fhir:ValueSet.compose.include.concept.code [ fhir:value "230270009" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Frontotemporal dementia (disorder)" ] ], [
fhir:index 30;
fhir:ValueSet.compose.include.concept.code [ fhir:value "51928006" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "General paresis - neurosyphilis (disorder)" ] ], [
fhir:index 31;
fhir:ValueSet.compose.include.concept.code [ fhir:value "88611000119100" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "History of traumatic brain injury (situation)" ] ], [
fhir:index 32;
fhir:ValueSet.compose.include.concept.code [ fhir:value "386806002" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Impaired cognition (finding)" ] ], [
fhir:index 33;
fhir:ValueSet.compose.include.concept.code [ fhir:value "2438005" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Iniencephaly (disorder)" ] ], [
fhir:index 34;
fhir:ValueSet.compose.include.concept.code [ fhir:value "110359009" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Intellectual disability (disorder)" ] ], [
fhir:index 35;
fhir:ValueSet.compose.include.concept.code [ fhir:value "792004" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Jakob-Creutzfeldt disease (disorder)" ] ], [
fhir:index 36;
fhir:ValueSet.compose.include.concept.code [ fhir:value "39925003" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (disorder)" ] ], [
fhir:index 37;
fhir:ValueSet.compose.include.concept.code [ fhir:value "25792000" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Kearns-Sayre syndrome (disorder)" ] ], [
fhir:index 38;
fhir:ValueSet.compose.include.concept.code [ fhir:value "405773007" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Kyphoscoliosis deformity of spine (disorder)" ] ], [
fhir:index 39;
fhir:ValueSet.compose.include.concept.code [ fhir:value "414667000" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Meningomyelocele (disorder)" ] ], [
fhir:index 40;
fhir:ValueSet.compose.include.concept.code [ fhir:value "47437004" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Mental handicap (finding)" ] ], [
fhir:index 41;
fhir:ValueSet.compose.include.concept.code [ fhir:value "718214007" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder)" ] ], [
fhir:index 42;
fhir:ValueSet.compose.include.concept.code [ fhir:value "447292006" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Mitochondrial encephalomyopathy (disorder)" ] ], [
fhir:index 43;
fhir:ValueSet.compose.include.concept.code [ fhir:value "56267009" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Multi-infarct dementia (disorder)" ] ], [
fhir:index 44;
fhir:ValueSet.compose.include.concept.code [ fhir:value "24700007" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Multiple sclerosis (disorder)" ] ], [
fhir:index 45;
fhir:ValueSet.compose.include.concept.code [ fhir:value "240046001" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Muscular dystrophy with predominantly proximal limb girdle distribution (disorder)" ] ], [
fhir:index 46;
fhir:ValueSet.compose.include.concept.code [ fhir:value "73297009" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Muscular dystrophy (disorder)" ] ], [
fhir:index 47;
fhir:ValueSet.compose.include.concept.code [ fhir:value "91637004" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Myasthenia gravis (disorder)" ] ], [
fhir:index 48;
fhir:ValueSet.compose.include.concept.code [ fhir:value "230426003" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Myoclonic epilepsy with ragged red fibers (disorder)" ] ], [
fhir:index 49;
fhir:ValueSet.compose.include.concept.code [ fhir:value "253098009" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Neural tube defect (disorder)" ] ], [
fhir:index 50;
fhir:ValueSet.compose.include.concept.code [ fhir:value "230572002" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Neuropathy due to diabetes mellitus (disorder)" ] ], [
fhir:index 51;
fhir:ValueSet.compose.include.concept.code [ fhir:value "386033004" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Neuropathy (disorder)" ] ], [
fhir:index 52;
fhir:ValueSet.compose.include.concept.code [ fhir:value "44695005" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Paralysis (finding)" ] ], [
fhir:index 53;
fhir:ValueSet.compose.include.concept.code [ fhir:value "29426003" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Paralytic syndrome (disorder)" ] ], [
fhir:index 54;
fhir:ValueSet.compose.include.concept.code [ fhir:value "32798002" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Parkinsonism (disorder)" ] ], [
fhir:index 55;
fhir:ValueSet.compose.include.concept.code [ fhir:value "49049000" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Parkinson's disease (disorder)" ] ], [
fhir:index 56;
fhir:ValueSet.compose.include.concept.code [ fhir:value "237985009" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Pearson's syndrome (disorder)" ] ], [
fhir:index 57;
fhir:ValueSet.compose.include.concept.code [ fhir:value "302226006" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Peripheral nerve disease (disorder)" ] ], [
fhir:index 58;
fhir:ValueSet.compose.include.concept.code [ fhir:value "35919005" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Pervasive developmental disorder (disorder)" ] ], [
fhir:index 59;
fhir:ValueSet.compose.include.concept.code [ fhir:value "5335002" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Phosphoenolpyruvate carboxykinase deficiency (disorder)" ] ], [
fhir:index 60;
fhir:ValueSet.compose.include.concept.code [ fhir:value "87694001" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Pyruvate carboxylase deficiency (disorder)" ] ], [
fhir:index 61;
fhir:ValueSet.compose.include.concept.code [ fhir:value "46683007" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Pyruvate dehydrogenase complex deficiency (disorder)" ] ], [
fhir:index 62;
fhir:ValueSet.compose.include.concept.code [ fhir:value "11538006" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Quadriplegia (disorder)" ] ], [
fhir:index 63;
fhir:ValueSet.compose.include.concept.code [ fhir:value "298382003" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Scoliosis deformity of spine (disorder)" ] ], [
fhir:index 64;
fhir:ValueSet.compose.include.concept.code [ fhir:value "91175000" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Seizure (finding)" ] ], [
fhir:index 65;
fhir:ValueSet.compose.include.concept.code [ fhir:value "128613002" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Seizure disorder (disorder)" ] ], [
fhir:index 66;
fhir:ValueSet.compose.include.concept.code [ fhir:value "312991009" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Senile dementia of the Lewy body type (disorder)" ] ], [
fhir:index 67;
fhir:ValueSet.compose.include.concept.code [ fhir:value "67531005" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Spina bifida (disorder)" ] ], [
fhir:index 68;
fhir:ValueSet.compose.include.concept.code [ fhir:value "47311000119103" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Static encephalopathy (disorder)" ] ], [
fhir:index 69;
fhir:ValueSet.compose.include.concept.code [ fhir:value "77956009" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Steinert myotonic dystrophy syndrome (disorder)" ] ], [
fhir:index 70;
fhir:ValueSet.compose.include.concept.code [ fhir:value "127295002" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Traumatic brain injury (disorder)" ] ], [
fhir:index 71;
fhir:ValueSet.compose.include.concept.code [ fhir:value "429998004" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Vascular dementia (disorder)" ] ] ]
].
# - ontology header ------------------------------------------------------------
a owl:Ontology;
owl:imports fhir:fhir.ttl.
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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