{
  "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",
  "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"
      } ]
    } ]
  },
  "_filename": "ValueSet-elixhauser-neurological-movement-disorder-vs.json",
  "package_name": "hl7.fhir.us.mcode",
  "date": "2021-04-15T12:44:45+00:00",
  "publisher": "HL7 International Clinical Interoperability Council",
  "jurisdiction": [ {
    "coding": [ {
      "code": "US",
      "system": "urn:iso:std:iso:3166",
      "display": "United States of America"
    } ]
  } ],
  "name": "ElixhauserNeurologicalMovementDisorderVS",
  "type": null,
  "experimental": null,
  "resourceType": "ValueSet",
  "title": "Elixhauser Comorbid Condition Value Set for Neurological Movement Disorders",
  "package_version": "1.16.0",
  "status": "active",
  "id": "0cc2eddf-e3b7-409a-af2a-0407aac0a404",
  "kind": null,
  "url": "http://hl7.org/fhir/us/mcode/ValueSet/elixhauser-neurological-movement-disorder-vs",
  "version": "1.16.0",
  "contact": [ {
    "name": "HL7 International Clinical Interoperability Council",
    "telecom": [ {
      "value": "http://www.hl7.org/Special/committees/cic",
      "system": "url"
    }, {
      "value": "ciclist@lists.HL7.org",
      "system": "email"
    } ]
  } ]
}