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Resource ValueSet/FHIR Server from package hl7.fhir.us.covid19library#current (63 ms)

Package hl7.fhir.us.covid19library
Type ValueSet
Id Id
FHIR Version R4
Source http://hl7.org/fhir/us/covid19library/https://build.fhir.org/ig/HL7/fhir-COVID19Library-ig/ValueSet-covid19-underlying-neurolgic-condition-value-set.html
Url http://hl7.org/fhir/us/covid19library/ValueSet/covid19-underlying-neurolgic-condition-value-set
Version 1.0.0
Status active
Date 2022-07-25T12:22:40+00:00
Name COVID19UnderlyingNeuroligicConditionsVS
Title COVID-19 neurologic underlying condition reference set
Experimental False
Realm us
Authority hl7
Description A set of codes that describe underlying conditions of a neurologic nature for COVID19.
Copyright This value set includes content from SNOMED CT, which is copyright © 2002+ International Health Terminology Standards Development Organisation (IHTSDO), and distributed by agreement between IHTSDO and HL7. Implementer use of SNOMED CT is not covered by this agreement

Resources that use this resource

StructureDefinition
covid19-underlying-condition-observation COVID-19 Underlying Medical Condition observation
underlying-neuroligic-medical-condition COVID-19 neurologic underlying condition

Resources that this resource uses

CodeSystem
http://snomed.info/sct SNOMED CT (all versions)
http://snomed.info/sct SNOMED codes used in this IG
http://snomed.info/sct SNOMED CT Canada Immunizations


Narrative

Note: links and images are rebased to the (stated) source

  • Include these codes as defined in http://snomed.info/sct
    CodeDisplay
    26929004Alzheimer's disease (disorder)
    86044005Amyotrophic lateral sclerosis (disorder)
    89369001Anencephalus (disorder)
    23560001Asperger's disorder (disorder)
    406506008Attention deficit hyperactivity disorder (disorder)
    35253001Attention deficit hyperactivity disorder, predominantly inattentive type (disorder)
    408856003Autistic disorder (disorder)
    387732009Becker muscular dystrophy (disorder)
    230724001Cerebral amyloid angiopathy (disorder)
    390936003Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)
    128188000Cerebral palsy (disorder)
    51500006Complete trisomy 18 syndrome (disorder)
    41040004Complete trisomy 21 syndrome (disorder)
    111501005Congenital hereditary muscular dystrophy (disorder)
    32219008Craniorachischisis (disorder)
    67434000Cytochrome-c oxidase deficiency (disorder)
    124165006Deficiency of succinate dehydrogenase (disorder)
    281004Dementia associated with alcoholism (disorder)
    52448006Dementia (disorder)
    237995002Depletion of mitochondrial deoxyribonucleic acid (disorder)
    248290002Developmental delay (disorder)
    76670001Duchenne muscular dystrophy (disorder)
    111508004Emery-Dreifuss muscular dystrophy (disorder)
    55999004Encephalocele (disorder)
    84757009Epilepsy (disorder)
    399091004Facioscapulohumeral muscular dystrophy (disorder)
    41497008Febrile convulsion (finding)
    613003Fragile X syndrome (disorder)
    10394003Friedreich's ataxia (disorder)
    230270009Frontotemporal dementia (disorder)
    51928006General paresis - neurosyphilis (disorder)
    88611000119100History of traumatic brain injury (situation)
    386806002Impaired cognition (finding)
    2438005Iniencephaly (disorder)
    110359009Intellectual disability (disorder)
    792004Jakob-Creutzfeldt disease (disorder)
    39925003Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (disorder)
    25792000Kearns-Sayre syndrome (disorder)
    405773007Kyphoscoliosis deformity of spine (disorder)
    414667000Meningomyelocele (disorder)
    47437004Mental handicap (finding)
    718214007Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder)
    447292006Mitochondrial encephalomyopathy (disorder)
    56267009Multi-infarct dementia (disorder)
    24700007Multiple sclerosis (disorder)
    240046001Muscular dystrophy with predominantly proximal limb girdle distribution (disorder)
    73297009Muscular dystrophy (disorder)
    91637004Myasthenia gravis (disorder)
    230426003Myoclonic epilepsy with ragged red fibers (disorder)
    253098009Neural tube defect (disorder)
    230572002Neuropathy due to diabetes mellitus (disorder)
    386033004Neuropathy (disorder)
    44695005Paralysis (finding)
    29426003Paralytic syndrome (disorder)
    32798002Parkinsonism (disorder)
    49049000Parkinson's disease (disorder)
    237985009Pearson's syndrome (disorder)
    302226006Peripheral nerve disease (disorder)
    35919005Pervasive developmental disorder (disorder)
    5335002Phosphoenolpyruvate carboxykinase deficiency (disorder)
    87694001Pyruvate carboxylase deficiency (disorder)
    46683007Pyruvate dehydrogenase complex deficiency (disorder)
    11538006Quadriplegia (disorder)
    298382003Scoliosis deformity of spine (disorder)
    91175000Seizure (finding)
    128613002Seizure disorder (disorder)
    312991009Senile dementia of the Lewy body type (disorder)
    67531005Spina bifida (disorder)
    47311000119103Static encephalopathy (disorder)
    77956009Steinert myotonic dystrophy syndrome (disorder)
    127295002Traumatic brain injury (disorder)
    429998004Vascular dementia (disorder)

Source

{
  "resourceType" : "ValueSet",
  "id" : "covid19-underlying-neurolgic-condition-value-set",
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><ul><li>Include these codes as defined in <a href=\"http://www.snomed.org/\"><code>http://snomed.info/sct</code></a><table class=\"none\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td><a href=\"http://snomed.info/id/26929004\">26929004</a></td><td>Alzheimer's disease (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/86044005\">86044005</a></td><td>Amyotrophic lateral sclerosis (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/89369001\">89369001</a></td><td>Anencephalus (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/23560001\">23560001</a></td><td>Asperger's disorder (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/406506008\">406506008</a></td><td>Attention deficit hyperactivity disorder (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/35253001\">35253001</a></td><td>Attention deficit hyperactivity disorder, predominantly inattentive type (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/408856003\">408856003</a></td><td>Autistic disorder (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/387732009\">387732009</a></td><td>Becker muscular dystrophy (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/230724001\">230724001</a></td><td>Cerebral amyloid angiopathy (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/390936003\">390936003</a></td><td>Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/128188000\">128188000</a></td><td>Cerebral palsy (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/51500006\">51500006</a></td><td>Complete trisomy 18 syndrome (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/41040004\">41040004</a></td><td>Complete trisomy 21 syndrome (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/111501005\">111501005</a></td><td>Congenital hereditary muscular dystrophy (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/32219008\">32219008</a></td><td>Craniorachischisis (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/67434000\">67434000</a></td><td>Cytochrome-c oxidase deficiency (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/124165006\">124165006</a></td><td>Deficiency of succinate dehydrogenase (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/281004\">281004</a></td><td>Dementia associated with alcoholism (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/52448006\">52448006</a></td><td>Dementia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/237995002\">237995002</a></td><td>Depletion of mitochondrial deoxyribonucleic acid (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/248290002\">248290002</a></td><td>Developmental delay (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/76670001\">76670001</a></td><td>Duchenne muscular dystrophy (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/111508004\">111508004</a></td><td>Emery-Dreifuss muscular dystrophy (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/55999004\">55999004</a></td><td>Encephalocele (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/84757009\">84757009</a></td><td>Epilepsy (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/399091004\">399091004</a></td><td>Facioscapulohumeral muscular dystrophy (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/41497008\">41497008</a></td><td>Febrile convulsion (finding)</td></tr><tr><td><a href=\"http://snomed.info/id/613003\">613003</a></td><td>Fragile X syndrome (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/10394003\">10394003</a></td><td>Friedreich's ataxia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/230270009\">230270009</a></td><td>Frontotemporal dementia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/51928006\">51928006</a></td><td>General paresis - neurosyphilis (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/88611000119100\">88611000119100</a></td><td>History of traumatic brain injury (situation)</td></tr><tr><td><a href=\"http://snomed.info/id/386806002\">386806002</a></td><td>Impaired cognition (finding)</td></tr><tr><td><a href=\"http://snomed.info/id/2438005\">2438005</a></td><td>Iniencephaly (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/110359009\">110359009</a></td><td>Intellectual disability (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/792004\">792004</a></td><td>Jakob-Creutzfeldt disease (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/39925003\">39925003</a></td><td>Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/25792000\">25792000</a></td><td>Kearns-Sayre syndrome (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/405773007\">405773007</a></td><td>Kyphoscoliosis deformity of spine (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/414667000\">414667000</a></td><td>Meningomyelocele (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/47437004\">47437004</a></td><td>Mental handicap (finding)</td></tr><tr><td><a href=\"http://snomed.info/id/718214007\">718214007</a></td><td>Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/447292006\">447292006</a></td><td>Mitochondrial encephalomyopathy (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/56267009\">56267009</a></td><td>Multi-infarct dementia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/24700007\">24700007</a></td><td>Multiple sclerosis (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/240046001\">240046001</a></td><td>Muscular dystrophy with predominantly proximal limb girdle distribution (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/73297009\">73297009</a></td><td>Muscular dystrophy (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/91637004\">91637004</a></td><td>Myasthenia gravis (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/230426003\">230426003</a></td><td>Myoclonic epilepsy with ragged red fibers (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/253098009\">253098009</a></td><td>Neural tube defect (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/230572002\">230572002</a></td><td>Neuropathy due to diabetes mellitus (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/386033004\">386033004</a></td><td>Neuropathy (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/44695005\">44695005</a></td><td>Paralysis (finding)</td></tr><tr><td><a href=\"http://snomed.info/id/29426003\">29426003</a></td><td>Paralytic syndrome (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/32798002\">32798002</a></td><td>Parkinsonism (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/49049000\">49049000</a></td><td>Parkinson's disease (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/237985009\">237985009</a></td><td>Pearson's syndrome (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/302226006\">302226006</a></td><td>Peripheral nerve disease (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/35919005\">35919005</a></td><td>Pervasive developmental disorder (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/5335002\">5335002</a></td><td>Phosphoenolpyruvate carboxykinase deficiency (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/87694001\">87694001</a></td><td>Pyruvate carboxylase deficiency (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/46683007\">46683007</a></td><td>Pyruvate dehydrogenase complex deficiency (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/11538006\">11538006</a></td><td>Quadriplegia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/298382003\">298382003</a></td><td>Scoliosis deformity of spine (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/91175000\">91175000</a></td><td>Seizure (finding)</td></tr><tr><td><a href=\"http://snomed.info/id/128613002\">128613002</a></td><td>Seizure disorder (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/312991009\">312991009</a></td><td>Senile dementia of the Lewy body type (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/67531005\">67531005</a></td><td>Spina bifida (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/47311000119103\">47311000119103</a></td><td>Static encephalopathy (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/77956009\">77956009</a></td><td>Steinert myotonic dystrophy syndrome (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/127295002\">127295002</a></td><td>Traumatic brain injury (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/429998004\">429998004</a></td><td>Vascular dementia (disorder)</td></tr></table></li></ul></div>"
  },
  "url" : "http://hl7.org/fhir/us/covid19library/ValueSet/covid19-underlying-neurolgic-condition-value-set",
  "version" : "1.0.0",
  "name" : "COVID19UnderlyingNeuroligicConditionsVS",
  "title" : "COVID-19 neurologic underlying condition reference set",
  "status" : "active",
  "date" : "2022-07-25T12:22:40+00:00",
  "publisher" : "HL7 International - Clinical Information Modeling Initiative",
  "contact" : [
    {
      "name" : "HL7 International - Clinical Information Modeling Initiative",
      "telecom" : [
        {
          "system" : "url",
          "value" : "http://hl7.org/Special/committees/cimi"
        }
      ]
    },
    {
      "name" : "Logica",
      "telecom" : [
        {
          "system" : "url",
          "value" : "https://www.logicahealth.org/"
        }
      ]
    },
    {
      "name" : "HL7",
      "telecom" : [
        {
          "system" : "url",
          "value" : "https://www.hl7.org"
        }
      ]
    }
  ],
  "description" : "A set of codes that describe underlying conditions of a neurologic nature for COVID19.",
  "jurisdiction" : [
    {
      "coding" : [
        {
          "system" : "urn:iso:std:iso:3166",
          "code" : "US",
          "display" : "United States of America"
        }
      ]
    }
  ],
  "copyright" : "This value set includes content from SNOMED CT, which is copyright © 2002+ International Health Terminology Standards Development Organisation (IHTSDO), and distributed by agreement between IHTSDO and HL7. Implementer use of SNOMED CT is not covered by this agreement",
  "compose" : {
    "include" : [
      {
        "system" : "http://snomed.info/sct",
        "concept" : [
          {
            "code" : "26929004",
            "display" : "Alzheimer's disease (disorder)"
          },
          {
            "code" : "86044005",
            "display" : "Amyotrophic lateral sclerosis (disorder)"
          },
          {
            "code" : "89369001",
            "display" : "Anencephalus (disorder)"
          },
          {
            "code" : "23560001",
            "display" : "Asperger's disorder (disorder)"
          },
          {
            "code" : "406506008",
            "display" : "Attention deficit hyperactivity disorder (disorder)"
          },
          {
            "code" : "35253001",
            "display" : "Attention deficit hyperactivity disorder, predominantly inattentive type (disorder)"
          },
          {
            "code" : "408856003",
            "display" : "Autistic disorder (disorder)"
          },
          {
            "code" : "387732009",
            "display" : "Becker muscular dystrophy (disorder)"
          },
          {
            "code" : "230724001",
            "display" : "Cerebral amyloid angiopathy (disorder)"
          },
          {
            "code" : "390936003",
            "display" : "Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)"
          },
          {
            "code" : "128188000",
            "display" : "Cerebral palsy (disorder)"
          },
          {
            "code" : "51500006",
            "display" : "Complete trisomy 18 syndrome (disorder)"
          },
          {
            "code" : "41040004",
            "display" : "Complete trisomy 21 syndrome (disorder)"
          },
          {
            "code" : "111501005",
            "display" : "Congenital hereditary muscular dystrophy (disorder)"
          },
          {
            "code" : "32219008",
            "display" : "Craniorachischisis (disorder)"
          },
          {
            "code" : "67434000",
            "display" : "Cytochrome-c oxidase deficiency (disorder)"
          },
          {
            "code" : "124165006",
            "display" : "Deficiency of succinate dehydrogenase (disorder)"
          },
          {
            "code" : "281004",
            "display" : "Dementia associated with alcoholism (disorder)"
          },
          {
            "code" : "52448006",
            "display" : "Dementia (disorder)"
          },
          {
            "code" : "237995002",
            "display" : "Depletion of mitochondrial deoxyribonucleic acid (disorder)"
          },
          {
            "code" : "248290002",
            "display" : "Developmental delay (disorder)"
          },
          {
            "code" : "76670001",
            "display" : "Duchenne muscular dystrophy (disorder)"
          },
          {
            "code" : "111508004",
            "display" : "Emery-Dreifuss muscular dystrophy (disorder)"
          },
          {
            "code" : "55999004",
            "display" : "Encephalocele (disorder)"
          },
          {
            "code" : "84757009",
            "display" : "Epilepsy (disorder)"
          },
          {
            "code" : "399091004",
            "display" : "Facioscapulohumeral muscular dystrophy (disorder)"
          },
          {
            "code" : "41497008",
            "display" : "Febrile convulsion (finding)"
          },
          {
            "code" : "613003",
            "display" : "Fragile X syndrome (disorder)"
          },
          {
            "code" : "10394003",
            "display" : "Friedreich's ataxia (disorder)"
          },
          {
            "code" : "230270009",
            "display" : "Frontotemporal dementia (disorder)"
          },
          {
            "code" : "51928006",
            "display" : "General paresis - neurosyphilis (disorder)"
          },
          {
            "code" : "88611000119100",
            "display" : "History of traumatic brain injury (situation)"
          },
          {
            "code" : "386806002",
            "display" : "Impaired cognition (finding)"
          },
          {
            "code" : "2438005",
            "display" : "Iniencephaly (disorder)"
          },
          {
            "code" : "110359009",
            "display" : "Intellectual disability (disorder)"
          },
          {
            "code" : "792004",
            "display" : "Jakob-Creutzfeldt disease (disorder)"
          },
          {
            "code" : "39925003",
            "display" : "Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (disorder)"
          },
          {
            "code" : "25792000",
            "display" : "Kearns-Sayre syndrome (disorder)"
          },
          {
            "code" : "405773007",
            "display" : "Kyphoscoliosis deformity of spine (disorder)"
          },
          {
            "code" : "414667000",
            "display" : "Meningomyelocele (disorder)"
          },
          {
            "code" : "47437004",
            "display" : "Mental handicap (finding)"
          },
          {
            "code" : "718214007",
            "display" : "Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder)"
          },
          {
            "code" : "447292006",
            "display" : "Mitochondrial encephalomyopathy (disorder)"
          },
          {
            "code" : "56267009",
            "display" : "Multi-infarct dementia (disorder)"
          },
          {
            "code" : "24700007",
            "display" : "Multiple sclerosis (disorder)"
          },
          {
            "code" : "240046001",
            "display" : "Muscular dystrophy with predominantly proximal limb girdle distribution (disorder)"
          },
          {
            "code" : "73297009",
            "display" : "Muscular dystrophy (disorder)"
          },
          {
            "code" : "91637004",
            "display" : "Myasthenia gravis (disorder)"
          },
          {
            "code" : "230426003",
            "display" : "Myoclonic epilepsy with ragged red fibers (disorder)"
          },
          {
            "code" : "253098009",
            "display" : "Neural tube defect (disorder)"
          },
          {
            "code" : "230572002",
            "display" : "Neuropathy due to diabetes mellitus (disorder)"
          },
          {
            "code" : "386033004",
            "display" : "Neuropathy (disorder)"
          },
          {
            "code" : "44695005",
            "display" : "Paralysis (finding)"
          },
          {
            "code" : "29426003",
            "display" : "Paralytic syndrome (disorder)"
          },
          {
            "code" : "32798002",
            "display" : "Parkinsonism (disorder)"
          },
          {
            "code" : "49049000",
            "display" : "Parkinson's disease (disorder)"
          },
          {
            "code" : "237985009",
            "display" : "Pearson's syndrome (disorder)"
          },
          {
            "code" : "302226006",
            "display" : "Peripheral nerve disease (disorder)"
          },
          {
            "code" : "35919005",
            "display" : "Pervasive developmental disorder (disorder)"
          },
          {
            "code" : "5335002",
            "display" : "Phosphoenolpyruvate carboxykinase deficiency (disorder)"
          },
          {
            "code" : "87694001",
            "display" : "Pyruvate carboxylase deficiency (disorder)"
          },
          {
            "code" : "46683007",
            "display" : "Pyruvate dehydrogenase complex deficiency (disorder)"
          },
          {
            "code" : "11538006",
            "display" : "Quadriplegia (disorder)"
          },
          {
            "code" : "298382003",
            "display" : "Scoliosis deformity of spine (disorder)"
          },
          {
            "code" : "91175000",
            "display" : "Seizure (finding)"
          },
          {
            "code" : "128613002",
            "display" : "Seizure disorder (disorder)"
          },
          {
            "code" : "312991009",
            "display" : "Senile dementia of the Lewy body type (disorder)"
          },
          {
            "code" : "67531005",
            "display" : "Spina bifida (disorder)"
          },
          {
            "code" : "47311000119103",
            "display" : "Static encephalopathy (disorder)"
          },
          {
            "code" : "77956009",
            "display" : "Steinert myotonic dystrophy syndrome (disorder)"
          },
          {
            "code" : "127295002",
            "display" : "Traumatic brain injury (disorder)"
          },
          {
            "code" : "429998004",
            "display" : "Vascular dementia (disorder)"
          }
        ]
      }
    ]
  }
}

XIG built as of ??metadata-date??. Found ??metadata-resources?? resources in ??metadata-packages?? packages.