{ "description": null, "compose": { "include": [ { "system": "http://snomed.info/sct", "concept": [ { "code": "10394003", "display": "Friedreich's ataxia (disorder)" }, { "code": "110359009", "display": "Intellectual disability (disorder)" }, { "code": "111501005", "display": "Congenital hereditary muscular dystrophy (disorder)" }, { "code": "111508004", "display": "Emery-Dreifuss muscular dystrophy (disorder)" }, { "code": "11538006", "display": "Quadriplegia (disorder)" }, { "code": "124165006", "display": "Deficiency of succinate dehydrogenase (disorder)" }, { "code": "127295002", "display": "Traumatic brain injury (disorder)" }, { "code": "128188000", "display": "Cerebral palsy (disorder)" }, { "code": "128613002", "display": "Seizure disorder (disorder)" }, { "code": "230270009", "display": "Frontotemporal dementia (disorder)" }, { "code": "230426003", "display": "Myoclonic epilepsy with ragged red fibers (disorder)" }, { "code": "230572002", "display": "Neuropathy due to diabetes mellitus (disorder)" }, { "code": "230724001", "display": "Cerebral amyloid angiopathy (disorder)" }, { "code": "23560001", "display": "Asperger's disorder (disorder)" }, { "code": "237985009", "display": "Pearson's syndrome (disorder)" }, { "code": "237995002", "display": "Depletion of mitochondrial deoxyribonucleic acid (disorder)" }, { "code": "240046001", "display": "Muscular dystrophy with predominantly proximal limb girdle distribution (disorder)" }, { "code": "2438005", "display": "Iniencephaly (disorder)" }, { "code": "24700007", "display": "Multiple sclerosis (disorder)" }, { "code": "248290002", "display": "Developmental delay (disorder)" }, { "code": "253098009", "display": "Neural tube defect (disorder)" }, { "code": "25792000", "display": "Kearns-Sayre syndrome (disorder)" }, { "code": "26929004", "display": "Alzheimer's disease (disorder)" }, { "code": "281004", "display": "Dementia associated with alcoholism (disorder)" }, { "code": "29426003", "display": "Paralytic syndrome (disorder)" }, { "code": "298382003", "display": "Scoliosis deformity of spine (disorder)" }, { "code": "302226006", "display": "Peripheral nerve disease (disorder)" }, { "code": "312991009", "display": "Senile dementia of the Lewy body type (disorder)" }, { "code": "32219008", "display": "Craniorachischisis (disorder)" }, { "code": "32798002", "display": "Parkinsonism (disorder)" }, { "code": "35253001", "display": "Attention deficit hyperactivity disorder, predominantly inattentive type (disorder)" }, { "code": "35919005", "display": "Pervasive developmental disorder (disorder)" }, { "code": "386033004", "display": "Neuropathy (disorder)" }, { "code": "386806002", "display": "Impaired cognition (finding)" }, { "code": "387732009", "display": "Becker muscular dystrophy (disorder)" }, { "code": "390936003", "display": "Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)" }, { "code": "399091004", "display": "Facioscapulohumeral muscular dystrophy (disorder)" }, { "code": "39925003", "display": "Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (disorder)" }, { "code": "405773007", "display": "Kyphoscoliosis deformity of spine (disorder)" }, { "code": "406506008", "display": "Attention deficit hyperactivity disorder (disorder)" }, { "code": "408856003", "display": "Autistic disorder (disorder)" }, { "code": "41040004", "display": "Complete trisomy 21 syndrome (disorder)" }, { "code": "414667000", "display": "Meningomyelocele (disorder)" }, { "code": "41497008", "display": "Febrile convulsion (finding)" }, { "code": "429998004", "display": "Vascular dementia (disorder)" }, { "code": "44695005", "display": "Paralysis (finding)" }, { "code": "447292006", "display": "Mitochondrial encephalomyopathy (disorder)" }, { "code": "46683007", "display": "Pyruvate dehydrogenase complex deficiency (disorder)" }, { "code": "47311000119103", "display": "Static encephalopathy (disorder)" }, { "code": "47437004", "display": "Mental handicap (finding)" }, { "code": "49049000", "display": "Parkinson's disease (disorder)" }, { "code": "51500006", "display": "Complete trisomy 18 syndrome (disorder)" }, { "code": "51928006", "display": "General paresis - neurosyphilis (disorder)" }, { "code": "52448006", "display": "Dementia (disorder)" }, { "code": "5335002", "display": "Phosphoenolpyruvate carboxykinase deficiency (disorder)" }, { "code": "55999004", "display": "Encephalocele (disorder)" }, { "code": "56267009", "display": "Multi-infarct dementia (disorder)" }, { "code": "613003", "display": "Fragile X syndrome (disorder)" }, { "code": "67434000", "display": "Cytochrome-c oxidase deficiency (disorder)" }, { "code": "67531005", "display": "Spina bifida (disorder)" }, { "code": "718214007", "display": "Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder)" }, { "code": "73297009", "display": "Muscular dystrophy (disorder)" }, { "code": "76670001", "display": "Duchenne muscular dystrophy (disorder)" }, { "code": "77956009", "display": "Steinert myotonic dystrophy syndrome (disorder)" }, { "code": "792004", "display": "Jakob-Creutzfeldt disease (disorder)" }, { "code": "84757009", "display": "Epilepsy (disorder)" }, { "code": "86044005", "display": "Amyotrophic lateral sclerosis (disorder)" }, { "code": "87694001", "display": "Pyruvate carboxylase deficiency (disorder)" }, { "code": "88611000119100", "display": "History of traumatic brain injury (situation)" }, { "code": "89369001", "display": "Anencephalus (disorder)" }, { "code": "91175000", "display": "Seizure (finding)" }, { "code": "91637004", "display": "Myasthenia gravis (disorder)" } ], "version": "http://snomed.info/sct/731000124108/version/20220301" } ] }, "_filename": "ValueSet-2.16.840.1.113762.1.4.1181.64.json", "package_name": "us.nlm.vsac", "date": "2020-09-03T01:00:25-04:00", "meta": { "versionId": "14", "lastUpdated": "2020-09-03T01:00:25.000-04:00" }, "publisher": "HSPC Steward", "name": "COVID19 neurologic underlying condition reference set", "type": null, "experimental": null, "resourceType": "ValueSet", "title": null, "package_version": "0.5.0", "status": "active", "id": "e625978e-1b89-42aa-9b15-f168be57e15d", "kind": null, "url": "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1181.64", "version": "20200903" }