COVID-19 FHIR Profile Library IG Informative Version
1.0.0 - Informative United States of America flag

COVID-19 FHIR Profile Library IG Informative Version, published by HL7 International - Clinical Information Modeling Initiative. This is not an authorized publication; it is the continuous build for version 1.0.0). This version is based on the current content of https://github.com/HL7/fhir-COVID19Library-ig/ and changes regularly. See the Directory of published versions

ValueSet: COVID-19 neurologic underlying condition reference set

Official URL: http://hl7.org/fhir/us/covid19library/ValueSet/covid19-underlying-neurolgic-condition-value-set Version: 1.0.0
Active as of 2022-07-25 Computable Name: COVID19UnderlyingNeuroligicConditionsVS

Copyright/Legal: 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

A set of codes that describe underlying conditions of a neurologic nature for COVID19.

References

Logical Definition (CLD)

  • 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)

 

Expansion

This value set contains 72 concepts

Expansion based on SNOMED CT United States edition 01-Mar 2022

All codes in this table are from the system 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)

Explanation of the columns that may appear on this page:

Level A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies
System The source of the definition of the code (when the value set draws in codes defined elsewhere)
Code The code (used as the code in the resource instance)
Display The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application
Definition An explanation of the meaning of the concept
Comments Additional notes about how to use the code