COVID-19 FHIR Profile Library IG
0.13.0 - 1st Comment Ballot

This page is part of the Logica COVID-19 FHIR Profile Library IG (v0.13.0: Drafts Ballot 1) based on FHIR R4. The current version which supercedes this version is 1.0.0. For a full list of available versions, see the Directory of published versions

ValueSet: COVID-19 neurologic underlying condition reference set

Summary

Defining URL:http://hl7.org/fhir/us/covid19library/ValueSet/covid19-underlying-neurolgic-condition-value-set
Version:0.13.0
Name:COVID19UnderlyingNeuroligicConditionsVS
Title:COVID-19 neurologic underlying condition reference set
Status:Active as of 2021-08-27T17:17:04+00:00
Definition:

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

Publisher:HL7 International - Clinical Information Modeling Initiative
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

Source Resource:XML / JSON / Turtle

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 2021

All codes from system http://snomed.info/sct

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