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: Elixhauser Neurological Movement Disorder Value Set - TTL Representation

Active as of 2023-03-21

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@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:id [ fhir:v "elixhauser-neurological-movement-disorder-vs"] ; # 
  fhir:text [
fhir:status [ fhir:v "generated" ] ;
fhir:div "<div xmlns=\"http://www.w3.org/1999/xhtml\"><ul><li>Include these codes as defined in <a href=\"http://terminology.hl7.org/5.0.0/CodeSystem-icd10CM.html\"><code>http://hl7.org/fhir/sid/icd-10-cm</code></a><table class=\"none\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td>G08</td><td>Intracranial and intraspinal phlebitis and thrombophlebitis</td></tr><tr><td>G10</td><td>Huntington's disease</td></tr><tr><td>G11.0</td><td>Congenital nonprogressive ataxia</td></tr><tr><td>G11.1</td><td>Early-onset cerebellar ataxia</td></tr><tr><td>G11.10</td><td>Early-onset cerebellar ataxia, unspecified</td></tr><tr><td>G11.11</td><td>Friedreich ataxia</td></tr><tr><td>G11.19</td><td>Other early-onset cerebellar ataxia</td></tr><tr><td>G11.2</td><td>Late-onset cerebellar ataxia</td></tr><tr><td>G11.3</td><td>Cerebellar ataxia with defective DNA repair</td></tr><tr><td>G11.4</td><td>Hereditary spastic paraplegia</td></tr><tr><td>G11.8</td><td>Other hereditary ataxias</td></tr><tr><td>G11.9</td><td>Hereditary ataxia, unspecified</td></tr><tr><td>G12.0</td><td>Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]</td></tr><tr><td>G12.1</td><td>Other inherited spinal muscular atrophy</td></tr><tr><td>G12.20</td><td>Motor neuron disease, unspecified</td></tr><tr><td>G12.21</td><td>Amyotrophic lateral sclerosis</td></tr><tr><td>G12.22</td><td>Progressive bulbar palsy</td></tr><tr><td>G12.23</td><td>Primary lateral sclerosis</td></tr><tr><td>G12.24</td><td>Familial motor neuron disease</td></tr><tr><td>G12.25</td><td>Progressive spinal muscle atrophy</td></tr><tr><td>G12.29</td><td>Other motor neuron disease</td></tr><tr><td>G12.8</td><td>Other spinal muscular atrophies and related syndromes</td></tr><tr><td>G12.9</td><td>Spinal muscular atrophy, unspecified</td></tr><tr><td>G13.0</td><td>Paraneoplastic neuromyopathy and neuropathy</td></tr><tr><td>G13.1</td><td>Other systemic atrophy primarily affecting central nervous system in neoplastic disease</td></tr><tr><td>G13.2</td><td>Systemic atrophy primarily affecting the cnsl in myxedema</td></tr><tr><td>G13.8</td><td>Systemic atrophy aff cnsl in oth diseases classd elswhr</td></tr><tr><td>G20</td><td>Parkinson's disease</td></tr><tr><td>G21.0</td><td>Malignant neuroleptic syndrome</td></tr><tr><td>G21.11</td><td>Neuroleptic induced parkinsonism</td></tr><tr><td>G21.19</td><td>Other drug induced secondary parkinsonism</td></tr><tr><td>G21.2</td><td>Secondary parkinsonism due to other external agents</td></tr><tr><td>G21.3</td><td>Postencephalitic parkinsonism</td></tr><tr><td>G21.4</td><td>Vascular parkinsonism</td></tr><tr><td>G21.8</td><td>Other secondary parkinsonism</td></tr><tr><td>G21.9</td><td>Secondary parkinsonism, unspecified</td></tr><tr><td>G23.0</td><td>Hallervorden-Spatz disease</td></tr><tr><td>G23.1</td><td>Progressive supranuclear ophthalmoplegia</td></tr><tr><td>G23.2</td><td>Striatonigral degeneration</td></tr><tr><td>G23.8</td><td>Other specified degenerative diseases of basal ganglia</td></tr><tr><td>G23.9</td><td>Degenerative disease of basal ganglia, unspecified</td></tr><tr><td>G24.09</td><td>Other drug induced dystonia</td></tr><tr><td>G24.1</td><td>Genomic torsion dystonia</td></tr><tr><td>G24.2</td><td>Idiopathic nonfamilial dystonia</td></tr><tr><td>G24.8</td><td>Other dystonia</td></tr><tr><td>G25.4</td><td>Drug-induced chorea</td></tr><tr><td>G25.5</td><td>Other chorea</td></tr><tr><td>G25.70</td><td>Drug induced movement disorder, unspecified</td></tr><tr><td>G25.71</td><td>Drug induced akathisia</td></tr><tr><td>G25.79</td><td>Other drug induced movement disorders</td></tr><tr><td>G25.81</td><td>Restless legs syndrome</td></tr><tr><td>G25.82</td><td>Stiff-man syndrome</td></tr><tr><td>G25.83</td><td>Benign shuddering attacks</td></tr><tr><td>G25.89</td><td>Other specified extrapyramidal and movement disorders</td></tr><tr><td>G25.9</td><td>Extrapyramidal and movement disorder, unspecified</td></tr><tr><td>G26</td><td>Extrapyramidal and movement disord in diseases classd elswhr</td></tr><tr><td>G32.0</td><td>Subac comb degeneration of spinal cord in dis classd elswhr</td></tr><tr><td>G32.81</td><td>Cerebellar ataxia in diseases classified elsewhere</td></tr><tr><td>G32.89</td><td>Oth degeneratv disord of nervous sys in dis classd elswhr</td></tr><tr><td>G80.3</td><td>Athetoid cerebral palsy</td></tr></table></li></ul></div>"
  ] ; # 
  fhir:url [ fhir:v "http://hl7.org/fhir/us/mcode/ValueSet/elixhauser-neurological-movement-disorder-vs"^^xsd:anyURI] ; # 
  fhir:version [ fhir:v "2.1.0"] ; # 
  fhir:name [ fhir:v "ElixhauserNeurologicalMovementDisorderVS"] ; # 
  fhir:title [ fhir:v "Elixhauser Neurological Movement Disorder Value Set"] ; # 
  fhir:status [ fhir:v "active"] ; # 
  fhir:experimental [ fhir:v "false"^^xsd:boolean] ; # 
  fhir:date [ fhir:v "2023-03-21T04:50:14+11:00"^^xsd:dateTime] ; # 
  fhir:publisher [ fhir:v "HL7 International Clinical Interoperability Council"] ; # 
  fhir:contact ( [
fhir:name [ fhir:v "HL7 International Clinical Interoperability Council" ] ;
    ( fhir:telecom [
fhir:system [ fhir:v "url" ] ;
fhir:value [ fhir:v "http://www.hl7.org/Special/committees/cic" ]     ] [
fhir:system [ fhir:v "email" ] ;
fhir:value [ fhir:v "ciclist@lists.HL7.org" ]     ] )
  ] ) ; # 
  fhir:description [ fhir:v "Elixhauser Comorbid Condition Value Set for Neurological Movement Disorders. ICD-10 codes are drawn from https://www.hcup-us.ahrq.gov/toolssoftware/comorbidityicd10/comorbidity_icd10.jsp, version 2021.1"] ; # 
  fhir:jurisdiction ( [
    ( fhir:coding [
fhir:system [ fhir:v "urn:iso:std:iso:3166"^^xsd:anyURI ] ;
fhir:code [ fhir:v "US" ] ;
fhir:display [ fhir:v "United States of America" ]     ] )
  ] ) ; # 
  fhir:compose [
    ( fhir:include [
fhir:system [ fhir:v "http://hl7.org/fhir/sid/icd-10-cm"^^xsd:anyURI ] ;
      ( fhir:concept [
fhir:code [ fhir:v "G08" ] ;
fhir:display [ fhir:v "Intracranial and intraspinal phlebitis and thrombophlebitis" ]       ] [
fhir:code [ fhir:v "G10" ] ;
fhir:display [ fhir:v "Huntington's disease" ]       ] [
fhir:code [ fhir:v "G11.0" ] ;
fhir:display [ fhir:v "Congenital nonprogressive ataxia" ]       ] [
fhir:code [ fhir:v "G11.1" ] ;
fhir:display [ fhir:v "Early-onset cerebellar ataxia" ]       ] [
fhir:code [ fhir:v "G11.10" ] ;
fhir:display [ fhir:v "Early-onset cerebellar ataxia, unspecified" ]       ] [
fhir:code [ fhir:v "G11.11" ] ;
fhir:display [ fhir:v "Friedreich ataxia" ]       ] [
fhir:code [ fhir:v "G11.19" ] ;
fhir:display [ fhir:v "Other early-onset cerebellar ataxia" ]       ] [
fhir:code [ fhir:v "G11.2" ] ;
fhir:display [ fhir:v "Late-onset cerebellar ataxia" ]       ] [
fhir:code [ fhir:v "G11.3" ] ;
fhir:display [ fhir:v "Cerebellar ataxia with defective DNA repair" ]       ] [
fhir:code [ fhir:v "G11.4" ] ;
fhir:display [ fhir:v "Hereditary spastic paraplegia" ]       ] [
fhir:code [ fhir:v "G11.8" ] ;
fhir:display [ fhir:v "Other hereditary ataxias" ]       ] [
fhir:code [ fhir:v "G11.9" ] ;
fhir:display [ fhir:v "Hereditary ataxia, unspecified" ]       ] [
fhir:code [ fhir:v "G12.0" ] ;
fhir:display [ fhir:v "Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]" ]       ] [
fhir:code [ fhir:v "G12.1" ] ;
fhir:display [ fhir:v "Other inherited spinal muscular atrophy" ]       ] [
fhir:code [ fhir:v "G12.20" ] ;
fhir:display [ fhir:v "Motor neuron disease, unspecified" ]       ] [
fhir:code [ fhir:v "G12.21" ] ;
fhir:display [ fhir:v "Amyotrophic lateral sclerosis" ]       ] [
fhir:code [ fhir:v "G12.22" ] ;
fhir:display [ fhir:v "Progressive bulbar palsy" ]       ] [
fhir:code [ fhir:v "G12.23" ] ;
fhir:display [ fhir:v "Primary lateral sclerosis" ]       ] [
fhir:code [ fhir:v "G12.24" ] ;
fhir:display [ fhir:v "Familial motor neuron disease" ]       ] [
fhir:code [ fhir:v "G12.25" ] ;
fhir:display [ fhir:v "Progressive spinal muscle atrophy" ]       ] [
fhir:code [ fhir:v "G12.29" ] ;
fhir:display [ fhir:v "Other motor neuron disease" ]       ] [
fhir:code [ fhir:v "G12.8" ] ;
fhir:display [ fhir:v "Other spinal muscular atrophies and related syndromes" ]       ] [
fhir:code [ fhir:v "G12.9" ] ;
fhir:display [ fhir:v "Spinal muscular atrophy, unspecified" ]       ] [
fhir:code [ fhir:v "G13.0" ] ;
fhir:display [ fhir:v "Paraneoplastic neuromyopathy and neuropathy" ]       ] [
fhir:code [ fhir:v "G13.1" ] ;
fhir:display [ fhir:v "Other systemic atrophy primarily affecting central nervous system in neoplastic disease" ]       ] [
fhir:code [ fhir:v "G13.2" ] ;
fhir:display [ fhir:v "Systemic atrophy primarily affecting the cnsl in myxedema" ]       ] [
fhir:code [ fhir:v "G13.8" ] ;
fhir:display [ fhir:v "Systemic atrophy aff cnsl in oth diseases classd elswhr" ]       ] [
fhir:code [ fhir:v "G20" ] ;
fhir:display [ fhir:v "Parkinson's disease" ]       ] [
fhir:code [ fhir:v "G21.0" ] ;
fhir:display [ fhir:v "Malignant neuroleptic syndrome" ]       ] [
fhir:code [ fhir:v "G21.11" ] ;
fhir:display [ fhir:v "Neuroleptic induced parkinsonism" ]       ] [
fhir:code [ fhir:v "G21.19" ] ;
fhir:display [ fhir:v "Other drug induced secondary parkinsonism" ]       ] [
fhir:code [ fhir:v "G21.2" ] ;
fhir:display [ fhir:v "Secondary parkinsonism due to other external agents" ]       ] [
fhir:code [ fhir:v "G21.3" ] ;
fhir:display [ fhir:v "Postencephalitic parkinsonism" ]       ] [
fhir:code [ fhir:v "G21.4" ] ;
fhir:display [ fhir:v "Vascular parkinsonism" ]       ] [
fhir:code [ fhir:v "G21.8" ] ;
fhir:display [ fhir:v "Other secondary parkinsonism" ]       ] [
fhir:code [ fhir:v "G21.9" ] ;
fhir:display [ fhir:v "Secondary parkinsonism, unspecified" ]       ] [
fhir:code [ fhir:v "G23.0" ] ;
fhir:display [ fhir:v "Hallervorden-Spatz disease" ]       ] [
fhir:code [ fhir:v "G23.1" ] ;
fhir:display [ fhir:v "Progressive supranuclear ophthalmoplegia" ]       ] [
fhir:code [ fhir:v "G23.2" ] ;
fhir:display [ fhir:v "Striatonigral degeneration" ]       ] [
fhir:code [ fhir:v "G23.8" ] ;
fhir:display [ fhir:v "Other specified degenerative diseases of basal ganglia" ]       ] [
fhir:code [ fhir:v "G23.9" ] ;
fhir:display [ fhir:v "Degenerative disease of basal ganglia, unspecified" ]       ] [
fhir:code [ fhir:v "G24.09" ] ;
fhir:display [ fhir:v "Other drug induced dystonia" ]       ] [
fhir:code [ fhir:v "G24.1" ] ;
fhir:display [ fhir:v "Genomic torsion dystonia" ]       ] [
fhir:code [ fhir:v "G24.2" ] ;
fhir:display [ fhir:v "Idiopathic nonfamilial dystonia" ]       ] [
fhir:code [ fhir:v "G24.8" ] ;
fhir:display [ fhir:v "Other dystonia" ]       ] [
fhir:code [ fhir:v "G25.4" ] ;
fhir:display [ fhir:v "Drug-induced chorea" ]       ] [
fhir:code [ fhir:v "G25.5" ] ;
fhir:display [ fhir:v "Other chorea" ]       ] [
fhir:code [ fhir:v "G25.70" ] ;
fhir:display [ fhir:v "Drug induced movement disorder, unspecified" ]       ] [
fhir:code [ fhir:v "G25.71" ] ;
fhir:display [ fhir:v "Drug induced akathisia" ]       ] [
fhir:code [ fhir:v "G25.79" ] ;
fhir:display [ fhir:v "Other drug induced movement disorders" ]       ] [
fhir:code [ fhir:v "G25.81" ] ;
fhir:display [ fhir:v "Restless legs syndrome" ]       ] [
fhir:code [ fhir:v "G25.82" ] ;
fhir:display [ fhir:v "Stiff-man syndrome" ]       ] [
fhir:code [ fhir:v "G25.83" ] ;
fhir:display [ fhir:v "Benign shuddering attacks" ]       ] [
fhir:code [ fhir:v "G25.89" ] ;
fhir:display [ fhir:v "Other specified extrapyramidal and movement disorders" ]       ] [
fhir:code [ fhir:v "G25.9" ] ;
fhir:display [ fhir:v "Extrapyramidal and movement disorder, unspecified" ]       ] [
fhir:code [ fhir:v "G26" ] ;
fhir:display [ fhir:v "Extrapyramidal and movement disord in diseases classd elswhr" ]       ] [
fhir:code [ fhir:v "G32.0" ] ;
fhir:display [ fhir:v "Subac comb degeneration of spinal cord in dis classd elswhr" ]       ] [
fhir:code [ fhir:v "G32.81" ] ;
fhir:display [ fhir:v "Cerebellar ataxia in diseases classified elsewhere" ]       ] [
fhir:code [ fhir:v "G32.89" ] ;
fhir:display [ fhir:v "Oth degeneratv disord of nervous sys in dis classd elswhr" ]       ] [
fhir:code [ fhir:v "G80.3" ] ;
fhir:display [ fhir:v "Athetoid cerebral palsy" ]       ] )     ] )
  ] . #