minimal Common Oncology Data Elements (mCODE) Implementation Guide
1.16.0 - STU Release 2 (Ballot Version)
minimal Common Oncology Data Elements (mCODE) Implementation Guide
1.16.0 - STU Release 2 (Ballot Version)
This page is part of the HL7 FHIR Implementation Guide: minimal Common Oncology Data Elements (mCODE) Release 1 - US Realm | STU1 (v1.16.0: STU 2 Ballot 1) based on FHIR R4. The current version which supercedes this version is 2.0.0. For a full list of available versions, see the Directory of published versions 
{
"resourceType" : "ValueSet",
"id" : "elixhauser-neurological-movement-disorder-vs",
"text" : {
"status" : "generated",
"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><ul><li>Include these codes as defined in <a href=\"https://terminology.hl7.org/1.0.0//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>Genetic 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>"
},
"url" : "http://hl7.org/fhir/us/mcode/ValueSet/elixhauser-neurological-movement-disorder-vs",
"version" : "1.16.0",
"name" : "ElixhauserNeurologicalMovementDisorderVS",
"title" : "Elixhauser Comorbid Condition Value Set for Neurological Movement Disorders",
"status" : "active",
"date" : "2021-04-15T12:44:45+00:00",
"publisher" : "HL7 International Clinical Interoperability Council",
"contact" : [
{
"name" : "HL7 International Clinical Interoperability Council",
"telecom" : [
{
"system" : "url",
"value" : "http://www.hl7.org/Special/committees/cic"
},
{
"system" : "email",
"value" : "ciclist@lists.HL7.org"
}
]
}
],
"description" : "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",
"jurisdiction" : [
{
"coding" : [
{
"system" : "urn:iso:std:iso:3166",
"code" : "US",
"display" : "United States of America"
}
]
}
],
"compose" : {
"include" : [
{
"system" : "http://hl7.org/fhir/sid/icd-10-cm",
"concept" : [
{
"code" : "G08",
"display" : "Intracranial and intraspinal phlebitis and thrombophlebitis"
},
{
"code" : "G10",
"display" : "Huntington's disease"
},
{
"code" : "G11.0",
"display" : "Congenital nonprogressive ataxia"
},
{
"code" : "G11.1",
"display" : "Early-onset cerebellar ataxia"
},
{
"code" : "G11.10",
"display" : "Early-onset cerebellar ataxia, unspecified"
},
{
"code" : "G11.11",
"display" : "Friedreich ataxia"
},
{
"code" : "G11.19",
"display" : "Other early-onset cerebellar ataxia"
},
{
"code" : "G11.2",
"display" : "Late-onset cerebellar ataxia"
},
{
"code" : "G11.3",
"display" : "Cerebellar ataxia with defective DNA repair"
},
{
"code" : "G11.4",
"display" : "Hereditary spastic paraplegia"
},
{
"code" : "G11.8",
"display" : "Other hereditary ataxias"
},
{
"code" : "G11.9",
"display" : "Hereditary ataxia, unspecified"
},
{
"code" : "G12.0",
"display" : "Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]"
},
{
"code" : "G12.1",
"display" : "Other inherited spinal muscular atrophy"
},
{
"code" : "G12.20",
"display" : "Motor neuron disease, unspecified"
},
{
"code" : "G12.21",
"display" : "Amyotrophic lateral sclerosis"
},
{
"code" : "G12.22",
"display" : "Progressive bulbar palsy"
},
{
"code" : "G12.23",
"display" : "Primary lateral sclerosis"
},
{
"code" : "G12.24",
"display" : "Familial motor neuron disease"
},
{
"code" : "G12.25",
"display" : "Progressive spinal muscle atrophy"
},
{
"code" : "G12.29",
"display" : "Other motor neuron disease"
},
{
"code" : "G12.8",
"display" : "Other spinal muscular atrophies and related syndromes"
},
{
"code" : "G12.9",
"display" : "Spinal muscular atrophy, unspecified"
},
{
"code" : "G13.0",
"display" : "Paraneoplastic neuromyopathy and neuropathy"
},
{
"code" : "G13.1",
"display" : "Other systemic atrophy primarily affecting central nervous system in neoplastic disease"
},
{
"code" : "G13.2",
"display" : "Systemic atrophy primarily affecting the cnsl in myxedema"
},
{
"code" : "G13.8",
"display" : "Systemic atrophy aff cnsl in oth diseases classd elswhr"
},
{
"code" : "G20",
"display" : "Parkinson's disease"
},
{
"code" : "G21.0",
"display" : "Malignant neuroleptic syndrome"
},
{
"code" : "G21.11",
"display" : "Neuroleptic induced parkinsonism"
},
{
"code" : "G21.19",
"display" : "Other drug induced secondary parkinsonism"
},
{
"code" : "G21.2",
"display" : "Secondary parkinsonism due to other external agents"
},
{
"code" : "G21.3",
"display" : "Postencephalitic parkinsonism"
},
{
"code" : "G21.4",
"display" : "Vascular parkinsonism"
},
{
"code" : "G21.8",
"display" : "Other secondary parkinsonism"
},
{
"code" : "G21.9",
"display" : "Secondary parkinsonism, unspecified"
},
{
"code" : "G23.0",
"display" : "Hallervorden-Spatz disease"
},
{
"code" : "G23.1",
"display" : "Progressive supranuclear ophthalmoplegia"
},
{
"code" : "G23.2",
"display" : "Striatonigral degeneration"
},
{
"code" : "G23.8",
"display" : "Other specified degenerative diseases of basal ganglia"
},
{
"code" : "G23.9",
"display" : "Degenerative disease of basal ganglia, unspecified"
},
{
"code" : "G24.09",
"display" : "Other drug induced dystonia"
},
{
"code" : "G24.1",
"display" : "Genetic torsion dystonia"
},
{
"code" : "G24.2",
"display" : "Idiopathic nonfamilial dystonia"
},
{
"code" : "G24.8",
"display" : "Other dystonia"
},
{
"code" : "G25.4",
"display" : "Drug-induced chorea"
},
{
"code" : "G25.5",
"display" : "Other chorea"
},
{
"code" : "G25.70",
"display" : "Drug induced movement disorder, unspecified"
},
{
"code" : "G25.71",
"display" : "Drug induced akathisia"
},
{
"code" : "G25.79",
"display" : "Other drug induced movement disorders"
},
{
"code" : "G25.81",
"display" : "Restless legs syndrome"
},
{
"code" : "G25.82",
"display" : "Stiff-man syndrome"
},
{
"code" : "G25.83",
"display" : "Benign shuddering attacks"
},
{
"code" : "G25.89",
"display" : "Other specified extrapyramidal and movement disorders"
},
{
"code" : "G25.9",
"display" : "Extrapyramidal and movement disorder, unspecified"
},
{
"code" : "G26",
"display" : "Extrapyramidal and movement disord in diseases classd elswhr"
},
{
"code" : "G32.0",
"display" : "Subac comb degeneration of spinal cord in dis classd elswhr"
},
{
"code" : "G32.81",
"display" : "Cerebellar ataxia in diseases classified elsewhere"
},
{
"code" : "G32.89",
"display" : "Oth degeneratv disord of nervous sys in dis classd elswhr"
},
{
"code" : "G80.3",
"display" : "Athetoid cerebral palsy"
}
]
}
]
}
}
IG © 2019+ HL7 International Clinical Interoperability Council. Package hl7.fhir.us.mcode#1.16.0 based on FHIR 4.0.1. Generated 2021-04-15
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