ValueSet-2.16.840.1.113762.1.4.1181.64

Sourceus.nlm.vsac#0.11.0:null (v4.0.1)
resourceTypeValueSet
id2.16.840.1.113762.1.4.1181.64
canonicalhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1181.64
version20200903
statusactive
publisherHSPC Steward
nameCOVID19NeurologicUnderlyingConditionReferenceSet
titleCOVID19 neurologic underlying condition reference set
date2020-09-03T01:00:25-04:00
experimentalfalse
Usages(none)

This value set contains 71 concepts

Code System Display
   10394003 http://snomed.info/sct Friedreich's ataxia (disorder)
   110359009 http://snomed.info/sct Intellectual disability (disorder)
   111501005 http://snomed.info/sct Congenital hereditary muscular dystrophy (disorder)
   111508004 http://snomed.info/sct Emery-Dreifuss muscular dystrophy (disorder)
   11538006 http://snomed.info/sct Quadriplegia (disorder)
   124165006 http://snomed.info/sct Deficiency of succinate dehydrogenase (disorder)
   127295002 http://snomed.info/sct Traumatic brain injury (disorder)
   128188000 http://snomed.info/sct Cerebral palsy (disorder)
   128613002 http://snomed.info/sct Seizure disorder (disorder)
   230270009 http://snomed.info/sct Frontotemporal dementia (disorder)
   230426003 http://snomed.info/sct Myoclonic epilepsy with ragged red fibers (disorder)
   230572002 http://snomed.info/sct Neuropathy due to diabetes mellitus (disorder)
   230724001 http://snomed.info/sct Cerebral amyloid angiopathy (disorder)
   23560001 http://snomed.info/sct Asperger's disorder (disorder)
   237985009 http://snomed.info/sct Pearson's syndrome (disorder)
   237995002 http://snomed.info/sct Depletion of mitochondrial deoxyribonucleic acid (disorder)
   240046001 http://snomed.info/sct Muscular dystrophy with predominantly proximal limb girdle distribution (disorder)
   2438005 http://snomed.info/sct Iniencephaly (disorder)
   24700007 http://snomed.info/sct Multiple sclerosis (disorder)
   248290002 http://snomed.info/sct Developmental delay (disorder)
   253098009 http://snomed.info/sct Neural tube defect (disorder)
   25792000 http://snomed.info/sct Kearns-Sayre syndrome (disorder)
   26929004 http://snomed.info/sct Alzheimer's disease (disorder)
   281004 http://snomed.info/sct Dementia associated with alcoholism (disorder)
   29426003 http://snomed.info/sct Paralytic syndrome (disorder)
   298382003 http://snomed.info/sct Scoliosis deformity of spine (disorder)
   302226006 http://snomed.info/sct Peripheral nerve disease (disorder)
   312991009 http://snomed.info/sct Senile dementia of the Lewy body type (disorder)
   32219008 http://snomed.info/sct Craniorachischisis (disorder)
   32798002 http://snomed.info/sct Parkinsonism (disorder)
   35253001 http://snomed.info/sct Attention deficit hyperactivity disorder, predominantly inattentive type (disorder)
   35919005 http://snomed.info/sct Pervasive developmental disorder (disorder)
   386033004 http://snomed.info/sct Neuropathy (disorder)
   386806002 http://snomed.info/sct Impaired cognition (finding)
   387732009 http://snomed.info/sct Becker muscular dystrophy (disorder)
   390936003 http://snomed.info/sct Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)
   399091004 http://snomed.info/sct Facioscapulohumeral muscular dystrophy (disorder)
   39925003 http://snomed.info/sct Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (disorder)
   405773007 http://snomed.info/sct Kyphoscoliosis deformity of spine (disorder)
   406506008 http://snomed.info/sct Attention deficit hyperactivity disorder (disorder)
   408856003 http://snomed.info/sct Autistic disorder (disorder)
   41040004 http://snomed.info/sct Complete trisomy 21 syndrome (disorder)
   414667000 http://snomed.info/sct Meningomyelocele (disorder)
   41497008 http://snomed.info/sct Febrile convulsion (finding)
   429998004 http://snomed.info/sct Vascular dementia (disorder)
   44695005 http://snomed.info/sct Paralysis (finding)
   447292006 http://snomed.info/sct Mitochondrial encephalomyopathy (disorder)
   46683007 http://snomed.info/sct Pyruvate dehydrogenase complex deficiency (disorder)
   47311000119103 http://snomed.info/sct Static encephalopathy (disorder)
   49049000 http://snomed.info/sct Parkinson's disease (disorder)
   51500006 http://snomed.info/sct Complete trisomy 18 syndrome (disorder)
   51928006 http://snomed.info/sct General paresis - neurosyphilis (disorder)
   52448006 http://snomed.info/sct Dementia (disorder)
   5335002 http://snomed.info/sct Phosphoenolpyruvate carboxykinase deficiency (disorder)
   55999004 http://snomed.info/sct Encephalocele (disorder)
   56267009 http://snomed.info/sct Multi-infarct dementia (disorder)
   613003 http://snomed.info/sct Fragile X syndrome (disorder)
   67434000 http://snomed.info/sct Cytochrome-c oxidase deficiency (disorder)
   67531005 http://snomed.info/sct Spina bifida (disorder)
   718214007 http://snomed.info/sct Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder)
   73297009 http://snomed.info/sct Muscular dystrophy (disorder)
   76670001 http://snomed.info/sct Duchenne muscular dystrophy (disorder)
   77956009 http://snomed.info/sct Steinert myotonic dystrophy syndrome (disorder)
   792004 http://snomed.info/sct Jakob-Creutzfeldt disease (disorder)
   84757009 http://snomed.info/sct Epilepsy (disorder)
   86044005 http://snomed.info/sct Amyotrophic lateral sclerosis (disorder)
   87694001 http://snomed.info/sct Pyruvate carboxylase deficiency (disorder)
   88611000119100 http://snomed.info/sct History of traumatic brain injury (situation)
   89369001 http://snomed.info/sct Anencephalus (disorder)
   91175000 http://snomed.info/sct Seizure (finding)
   91637004 http://snomed.info/sct Myasthenia gravis (disorder)

Produced 08 Sep 2023