FHIR IG Statistics: ValueSet/covid19-underlying-neurolgic-condition-value-set
Package | hl7.fhir.us.covid19library |
Type | ValueSet |
Id | covid19-underlying-neurolgic-condition-value-set |
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 |
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
CodeSystem |
sct | SNOMED CT (all versions) |
sct | SNOMED codes used in this IG |
sct | veri |
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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"text": {
"status": "generated",
"div": "<!-- snip (see above) -->"
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"url": "http://hl7.org/fhir/us/covid19library/ValueSet/covid19-underlying-neurolgic-condition-value-set",
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"name": "COVID19UnderlyingNeuroligicConditionsVS",
"title": "COVID-19 neurologic underlying condition reference set",
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"date": "2022-07-25T12:22:40+00:00",
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"jurisdiction": [
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"code": "US",
"display": "United States of America"
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],
"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)"
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}