minimal Common Oncology Data Elements (mCODE) Implementation Guide
2.0.0 - STU 2
minimal Common Oncology Data Elements (mCODE) Implementation Guide
2.0.0 - STU 2
This page is part of the HL7 FHIR Implementation Guide: minimal Common Oncology Data Elements (mCODE) Release 1 - US Realm | STU1 (v2.0.0: STU 2) based on FHIR R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions 
@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:Resource.id [ fhir:value "elixhauser-neurological-movement-disorder-vs"];
fhir:DomainResource.text [
fhir:Narrative.status [ fhir:value "generated" ];
fhir:Narrative.div "<div xmlns=\"http://www.w3.org/1999/xhtml\"><ul><li>Include these codes as defined in <a href=\"http://terminology.hl7.org/3.0.0/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:ValueSet.url [ fhir:value "http://hl7.org/fhir/us/mcode/ValueSet/elixhauser-neurological-movement-disorder-vs"];
fhir:ValueSet.version [ fhir:value "2.0.0"];
fhir:ValueSet.name [ fhir:value "ElixhauserNeurologicalMovementDisorderVS"];
fhir:ValueSet.title [ fhir:value "Elixhauser Neurological Movement Disorder Value Set"];
fhir:ValueSet.status [ fhir:value "active"];
fhir:ValueSet.date [ fhir:value "2022-01-18T03:17:40+00:00"^^xsd:dateTime];
fhir:ValueSet.publisher [ fhir:value "HL7 International Clinical Interoperability Council"];
fhir:ValueSet.contact [
fhir:index 0;
fhir:ContactDetail.name [ fhir:value "HL7 International Clinical Interoperability Council" ];
fhir:ContactDetail.telecom [
fhir:index 0;
fhir:ContactPoint.system [ fhir:value "url" ];
fhir:ContactPoint.value [ fhir:value "http://www.hl7.org/Special/committees/cic" ] ], [
fhir:index 1;
fhir:ContactPoint.system [ fhir:value "email" ];
fhir:ContactPoint.value [ fhir:value "ciclist@lists.HL7.org" ] ]
];
fhir:ValueSet.description [ fhir:value "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:ValueSet.jurisdiction [
fhir:index 0;
fhir:CodeableConcept.coding [
fhir:index 0;
fhir:Coding.system [ fhir:value "urn:iso:std:iso:3166" ];
fhir:Coding.code [ fhir:value "US" ];
fhir:Coding.display [ fhir:value "United States of America" ] ]
];
fhir:ValueSet.compose [
fhir:ValueSet.compose.include [
fhir:index 0;
fhir:ValueSet.compose.include.system [ fhir:value "http://hl7.org/fhir/sid/icd-10-cm" ];
fhir:ValueSet.compose.include.concept [
fhir:index 0;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G08" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Intracranial and intraspinal phlebitis and thrombophlebitis" ] ], [
fhir:index 1;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G10" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Huntington's disease" ] ], [
fhir:index 2;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G11.0" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Congenital nonprogressive ataxia" ] ], [
fhir:index 3;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G11.1" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Early-onset cerebellar ataxia" ] ], [
fhir:index 4;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G11.10" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Early-onset cerebellar ataxia, unspecified" ] ], [
fhir:index 5;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G11.11" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Friedreich ataxia" ] ], [
fhir:index 6;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G11.19" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Other early-onset cerebellar ataxia" ] ], [
fhir:index 7;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G11.2" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Late-onset cerebellar ataxia" ] ], [
fhir:index 8;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G11.3" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Cerebellar ataxia with defective DNA repair" ] ], [
fhir:index 9;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G11.4" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Hereditary spastic paraplegia" ] ], [
fhir:index 10;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G11.8" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Other hereditary ataxias" ] ], [
fhir:index 11;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G11.9" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Hereditary ataxia, unspecified" ] ], [
fhir:index 12;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G12.0" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]" ] ], [
fhir:index 13;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G12.1" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Other inherited spinal muscular atrophy" ] ], [
fhir:index 14;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G12.20" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Motor neuron disease, unspecified" ] ], [
fhir:index 15;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G12.21" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Amyotrophic lateral sclerosis" ] ], [
fhir:index 16;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G12.22" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Progressive bulbar palsy" ] ], [
fhir:index 17;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G12.23" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Primary lateral sclerosis" ] ], [
fhir:index 18;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G12.24" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Familial motor neuron disease" ] ], [
fhir:index 19;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G12.25" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Progressive spinal muscle atrophy" ] ], [
fhir:index 20;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G12.29" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Other motor neuron disease" ] ], [
fhir:index 21;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G12.8" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Other spinal muscular atrophies and related syndromes" ] ], [
fhir:index 22;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G12.9" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Spinal muscular atrophy, unspecified" ] ], [
fhir:index 23;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G13.0" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Paraneoplastic neuromyopathy and neuropathy" ] ], [
fhir:index 24;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G13.1" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Other systemic atrophy primarily affecting central nervous system in neoplastic disease" ] ], [
fhir:index 25;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G13.2" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Systemic atrophy primarily affecting the cnsl in myxedema" ] ], [
fhir:index 26;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G13.8" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Systemic atrophy aff cnsl in oth diseases classd elswhr" ] ], [
fhir:index 27;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G20" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Parkinson's disease" ] ], [
fhir:index 28;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G21.0" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Malignant neuroleptic syndrome" ] ], [
fhir:index 29;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G21.11" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Neuroleptic induced parkinsonism" ] ], [
fhir:index 30;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G21.19" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Other drug induced secondary parkinsonism" ] ], [
fhir:index 31;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G21.2" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Secondary parkinsonism due to other external agents" ] ], [
fhir:index 32;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G21.3" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Postencephalitic parkinsonism" ] ], [
fhir:index 33;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G21.4" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Vascular parkinsonism" ] ], [
fhir:index 34;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G21.8" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Other secondary parkinsonism" ] ], [
fhir:index 35;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G21.9" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Secondary parkinsonism, unspecified" ] ], [
fhir:index 36;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G23.0" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Hallervorden-Spatz disease" ] ], [
fhir:index 37;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G23.1" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Progressive supranuclear ophthalmoplegia" ] ], [
fhir:index 38;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G23.2" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Striatonigral degeneration" ] ], [
fhir:index 39;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G23.8" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Other specified degenerative diseases of basal ganglia" ] ], [
fhir:index 40;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G23.9" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Degenerative disease of basal ganglia, unspecified" ] ], [
fhir:index 41;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G24.09" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Other drug induced dystonia" ] ], [
fhir:index 42;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G24.1" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Genomic torsion dystonia" ] ], [
fhir:index 43;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G24.2" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Idiopathic nonfamilial dystonia" ] ], [
fhir:index 44;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G24.8" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Other dystonia" ] ], [
fhir:index 45;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G25.4" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Drug-induced chorea" ] ], [
fhir:index 46;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G25.5" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Other chorea" ] ], [
fhir:index 47;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G25.70" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Drug induced movement disorder, unspecified" ] ], [
fhir:index 48;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G25.71" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Drug induced akathisia" ] ], [
fhir:index 49;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G25.79" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Other drug induced movement disorders" ] ], [
fhir:index 50;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G25.81" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Restless legs syndrome" ] ], [
fhir:index 51;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G25.82" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Stiff-man syndrome" ] ], [
fhir:index 52;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G25.83" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Benign shuddering attacks" ] ], [
fhir:index 53;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G25.89" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Other specified extrapyramidal and movement disorders" ] ], [
fhir:index 54;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G25.9" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Extrapyramidal and movement disorder, unspecified" ] ], [
fhir:index 55;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G26" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Extrapyramidal and movement disord in diseases classd elswhr" ] ], [
fhir:index 56;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G32.0" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Subac comb degeneration of spinal cord in dis classd elswhr" ] ], [
fhir:index 57;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G32.81" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Cerebellar ataxia in diseases classified elsewhere" ] ], [
fhir:index 58;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G32.89" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Oth degeneratv disord of nervous sys in dis classd elswhr" ] ], [
fhir:index 59;
fhir:ValueSet.compose.include.concept.code [ fhir:value "G80.3" ];
fhir:ValueSet.compose.include.concept.display [ fhir:value "Athetoid cerebral palsy" ] ] ]
].
# - ontology header ------------------------------------------------------------
a owl:Ontology;
owl:imports fhir:fhir.ttl.
IG © 2019+ HL7 International Clinical Interoperability Council. Package hl7.fhir.us.mcode#2.0.0 based on FHIR 4.0.1. Generated 2022-01-18
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