Resource ValueSet/FHIR Server from package hl7.fhir.us.covid19library#current (94 ms)
| Package | hl7.fhir.us.covid19library |
| Type | ValueSet |
| Id | Id |
| FHIR Version | R4 |
| Source | http://hl7.org/fhir/us/covid19library/https://build.fhir.org/ig/HL7/fhir-COVID19Library-ig/ValueSet-covid19-underlying-neurolgic-condition-value-set.html |
| Url | http://hl7.org/fhir/us/covid19library/ValueSet/covid19-underlying-neurolgic-condition-value-set |
| Version | 1.0.0 |
| Status | active |
| Date | 2022-07-25T12:22:40+00:00 |
| Name | COVID19UnderlyingNeuroligicConditionsVS |
| Title | COVID-19 neurologic underlying condition reference set |
| Experimental | False |
| Realm | us |
| Authority | hl7 |
| Description | A set of codes that describe underlying conditions of a neurologic nature for COVID19. |
| Copyright | 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 |
Resources that use this resource
Resources that this resource uses
Narrative
Note: links and images are rebased to the (stated) source
- Include these codes as defined in
http://snomed.info/sct| Code | Display |
| 26929004 | Alzheimer's disease (disorder) |
| 86044005 | Amyotrophic lateral sclerosis (disorder) |
| 89369001 | Anencephalus (disorder) |
| 23560001 | Asperger's disorder (disorder) |
| 406506008 | Attention deficit hyperactivity disorder (disorder) |
| 35253001 | Attention deficit hyperactivity disorder, predominantly inattentive type (disorder) |
| 408856003 | Autistic disorder (disorder) |
| 387732009 | Becker muscular dystrophy (disorder) |
| 230724001 | Cerebral amyloid angiopathy (disorder) |
| 390936003 | Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) |
| 128188000 | Cerebral palsy (disorder) |
| 51500006 | Complete trisomy 18 syndrome (disorder) |
| 41040004 | Complete trisomy 21 syndrome (disorder) |
| 111501005 | Congenital hereditary muscular dystrophy (disorder) |
| 32219008 | Craniorachischisis (disorder) |
| 67434000 | Cytochrome-c oxidase deficiency (disorder) |
| 124165006 | Deficiency of succinate dehydrogenase (disorder) |
| 281004 | Dementia associated with alcoholism (disorder) |
| 52448006 | Dementia (disorder) |
| 237995002 | Depletion of mitochondrial deoxyribonucleic acid (disorder) |
| 248290002 | Developmental delay (disorder) |
| 76670001 | Duchenne muscular dystrophy (disorder) |
| 111508004 | Emery-Dreifuss muscular dystrophy (disorder) |
| 55999004 | Encephalocele (disorder) |
| 84757009 | Epilepsy (disorder) |
| 399091004 | Facioscapulohumeral muscular dystrophy (disorder) |
| 41497008 | Febrile convulsion (finding) |
| 613003 | Fragile X syndrome (disorder) |
| 10394003 | Friedreich's ataxia (disorder) |
| 230270009 | Frontotemporal dementia (disorder) |
| 51928006 | General paresis - neurosyphilis (disorder) |
| 88611000119100 | History of traumatic brain injury (situation) |
| 386806002 | Impaired cognition (finding) |
| 2438005 | Iniencephaly (disorder) |
| 110359009 | Intellectual disability (disorder) |
| 792004 | Jakob-Creutzfeldt disease (disorder) |
| 39925003 | Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (disorder) |
| 25792000 | Kearns-Sayre syndrome (disorder) |
| 405773007 | Kyphoscoliosis deformity of spine (disorder) |
| 414667000 | Meningomyelocele (disorder) |
| 47437004 | Mental handicap (finding) |
| 718214007 | Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder) |
| 447292006 | Mitochondrial encephalomyopathy (disorder) |
| 56267009 | Multi-infarct dementia (disorder) |
| 24700007 | Multiple sclerosis (disorder) |
| 240046001 | Muscular dystrophy with predominantly proximal limb girdle distribution (disorder) |
| 73297009 | Muscular dystrophy (disorder) |
| 91637004 | Myasthenia gravis (disorder) |
| 230426003 | Myoclonic epilepsy with ragged red fibers (disorder) |
| 253098009 | Neural tube defect (disorder) |
| 230572002 | Neuropathy due to diabetes mellitus (disorder) |
| 386033004 | Neuropathy (disorder) |
| 44695005 | Paralysis (finding) |
| 29426003 | Paralytic syndrome (disorder) |
| 32798002 | Parkinsonism (disorder) |
| 49049000 | Parkinson's disease (disorder) |
| 237985009 | Pearson's syndrome (disorder) |
| 302226006 | Peripheral nerve disease (disorder) |
| 35919005 | Pervasive developmental disorder (disorder) |
| 5335002 | Phosphoenolpyruvate carboxykinase deficiency (disorder) |
| 87694001 | Pyruvate carboxylase deficiency (disorder) |
| 46683007 | Pyruvate dehydrogenase complex deficiency (disorder) |
| 11538006 | Quadriplegia (disorder) |
| 298382003 | Scoliosis deformity of spine (disorder) |
| 91175000 | Seizure (finding) |
| 128613002 | Seizure disorder (disorder) |
| 312991009 | Senile dementia of the Lewy body type (disorder) |
| 67531005 | Spina bifida (disorder) |
| 47311000119103 | Static encephalopathy (disorder) |
| 77956009 | Steinert myotonic dystrophy syndrome (disorder) |
| 127295002 | Traumatic brain injury (disorder) |
| 429998004 | Vascular dementia (disorder) |
Source
{
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"id" : "covid19-underlying-neurolgic-condition-value-set",
"text" : {
"status" : "generated",
"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>"
},
"url" : "http://hl7.org/fhir/us/covid19library/ValueSet/covid19-underlying-neurolgic-condition-value-set",
"version" : "1.0.0",
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"title" : "COVID-19 neurologic underlying condition reference set",
"status" : "active",
"date" : "2022-07-25T12:22:40+00:00",
"publisher" : "HL7 International - Clinical Information Modeling Initiative",
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},
{
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],
"description" : "A set of codes that describe underlying conditions of a neurologic nature for COVID19.",
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"coding" : [
{
"system" : "urn:iso:std:iso:3166",
"code" : "US",
"display" : "United States of America"
}
]
}
],
"copyright" : "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" : "http://snomed.info/sct",
"concept" : [
{
"code" : "26929004",
"display" : "Alzheimer's disease (disorder)"
},
{
"code" : "86044005",
"display" : "Amyotrophic lateral sclerosis (disorder)"
},
{
"code" : "89369001",
"display" : "Anencephalus (disorder)"
},
{
"code" : "23560001",
"display" : "Asperger's disorder (disorder)"
},
{
"code" : "406506008",
"display" : "Attention deficit hyperactivity disorder (disorder)"
},
{
"code" : "35253001",
"display" : "Attention deficit hyperactivity disorder, predominantly inattentive type (disorder)"
},
{
"code" : "408856003",
"display" : "Autistic disorder (disorder)"
},
{
"code" : "387732009",
"display" : "Becker muscular dystrophy (disorder)"
},
{
"code" : "230724001",
"display" : "Cerebral amyloid angiopathy (disorder)"
},
{
"code" : "390936003",
"display" : "Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)"
},
{
"code" : "128188000",
"display" : "Cerebral palsy (disorder)"
},
{
"code" : "51500006",
"display" : "Complete trisomy 18 syndrome (disorder)"
},
{
"code" : "41040004",
"display" : "Complete trisomy 21 syndrome (disorder)"
},
{
"code" : "111501005",
"display" : "Congenital hereditary muscular dystrophy (disorder)"
},
{
"code" : "32219008",
"display" : "Craniorachischisis (disorder)"
},
{
"code" : "67434000",
"display" : "Cytochrome-c oxidase deficiency (disorder)"
},
{
"code" : "124165006",
"display" : "Deficiency of succinate dehydrogenase (disorder)"
},
{
"code" : "281004",
"display" : "Dementia associated with alcoholism (disorder)"
},
{
"code" : "52448006",
"display" : "Dementia (disorder)"
},
{
"code" : "237995002",
"display" : "Depletion of mitochondrial deoxyribonucleic acid (disorder)"
},
{
"code" : "248290002",
"display" : "Developmental delay (disorder)"
},
{
"code" : "76670001",
"display" : "Duchenne muscular dystrophy (disorder)"
},
{
"code" : "111508004",
"display" : "Emery-Dreifuss muscular dystrophy (disorder)"
},
{
"code" : "55999004",
"display" : "Encephalocele (disorder)"
},
{
"code" : "84757009",
"display" : "Epilepsy (disorder)"
},
{
"code" : "399091004",
"display" : "Facioscapulohumeral muscular dystrophy (disorder)"
},
{
"code" : "41497008",
"display" : "Febrile convulsion (finding)"
},
{
"code" : "613003",
"display" : "Fragile X syndrome (disorder)"
},
{
"code" : "10394003",
"display" : "Friedreich's ataxia (disorder)"
},
{
"code" : "230270009",
"display" : "Frontotemporal dementia (disorder)"
},
{
"code" : "51928006",
"display" : "General paresis - neurosyphilis (disorder)"
},
{
"code" : "88611000119100",
"display" : "History of traumatic brain injury (situation)"
},
{
"code" : "386806002",
"display" : "Impaired cognition (finding)"
},
{
"code" : "2438005",
"display" : "Iniencephaly (disorder)"
},
{
"code" : "110359009",
"display" : "Intellectual disability (disorder)"
},
{
"code" : "792004",
"display" : "Jakob-Creutzfeldt disease (disorder)"
},
{
"code" : "39925003",
"display" : "Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (disorder)"
},
{
"code" : "25792000",
"display" : "Kearns-Sayre syndrome (disorder)"
},
{
"code" : "405773007",
"display" : "Kyphoscoliosis deformity of spine (disorder)"
},
{
"code" : "414667000",
"display" : "Meningomyelocele (disorder)"
},
{
"code" : "47437004",
"display" : "Mental handicap (finding)"
},
{
"code" : "718214007",
"display" : "Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder)"
},
{
"code" : "447292006",
"display" : "Mitochondrial encephalomyopathy (disorder)"
},
{
"code" : "56267009",
"display" : "Multi-infarct dementia (disorder)"
},
{
"code" : "24700007",
"display" : "Multiple sclerosis (disorder)"
},
{
"code" : "240046001",
"display" : "Muscular dystrophy with predominantly proximal limb girdle distribution (disorder)"
},
{
"code" : "73297009",
"display" : "Muscular dystrophy (disorder)"
},
{
"code" : "91637004",
"display" : "Myasthenia gravis (disorder)"
},
{
"code" : "230426003",
"display" : "Myoclonic epilepsy with ragged red fibers (disorder)"
},
{
"code" : "253098009",
"display" : "Neural tube defect (disorder)"
},
{
"code" : "230572002",
"display" : "Neuropathy due to diabetes mellitus (disorder)"
},
{
"code" : "386033004",
"display" : "Neuropathy (disorder)"
},
{
"code" : "44695005",
"display" : "Paralysis (finding)"
},
{
"code" : "29426003",
"display" : "Paralytic syndrome (disorder)"
},
{
"code" : "32798002",
"display" : "Parkinsonism (disorder)"
},
{
"code" : "49049000",
"display" : "Parkinson's disease (disorder)"
},
{
"code" : "237985009",
"display" : "Pearson's syndrome (disorder)"
},
{
"code" : "302226006",
"display" : "Peripheral nerve disease (disorder)"
},
{
"code" : "35919005",
"display" : "Pervasive developmental disorder (disorder)"
},
{
"code" : "5335002",
"display" : "Phosphoenolpyruvate carboxykinase deficiency (disorder)"
},
{
"code" : "87694001",
"display" : "Pyruvate carboxylase deficiency (disorder)"
},
{
"code" : "46683007",
"display" : "Pyruvate dehydrogenase complex deficiency (disorder)"
},
{
"code" : "11538006",
"display" : "Quadriplegia (disorder)"
},
{
"code" : "298382003",
"display" : "Scoliosis deformity of spine (disorder)"
},
{
"code" : "91175000",
"display" : "Seizure (finding)"
},
{
"code" : "128613002",
"display" : "Seizure disorder (disorder)"
},
{
"code" : "312991009",
"display" : "Senile dementia of the Lewy body type (disorder)"
},
{
"code" : "67531005",
"display" : "Spina bifida (disorder)"
},
{
"code" : "47311000119103",
"display" : "Static encephalopathy (disorder)"
},
{
"code" : "77956009",
"display" : "Steinert myotonic dystrophy syndrome (disorder)"
},
{
"code" : "127295002",
"display" : "Traumatic brain injury (disorder)"
},
{
"code" : "429998004",
"display" : "Vascular dementia (disorder)"
}
]
}
]
}
}
XIG built as of ??metadata-date??. Found ??metadata-resources?? resources in ??metadata-packages?? packages.
FHIR