FHIR IG analytics
| Package | us.nlm.vsac |
| Resource Type | ValueSet |
| Id | ValueSet-2.16.840.1.113762.1.4.1219.48.json |
| FHIR Version | R4 |
| Source | https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1219.48/expansion |
| URL | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1219.48 |
| Version | 20220315 |
| Status | active |
| Date | 2022-03-15T01:04:14-04:00 |
| Name | VentilatorTherapyQualifyingCondition |
| Title | Ventilator Therapy Qualifying Condition |
| Realm | us |
| Authority | hl7 |
| Purpose | (Clinical Focus: Conditions that may qualify a patient to receive ventilator treatment.),(Data Element Scope: Conditions identified by U.S. Centers for Medicare and Medicaid that may justify use of a ventilator.),(Inclusion Criteria: Restrictive lung disease, motor neuron disease, spinal muscular atrophy, chronic respiratory failure, chest wall deformity.),(Exclusion Criteria: No exclusions) |
Resources that use this resource
No resources found
Resources that this resource uses
| CodeSystem |
| icd-10-cm | International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM) |
| sct | SNOMED codes used in this IG |
Narrative
No narrative content found in resource
Source1
{
"resourceType": "ValueSet",
"id": "2.16.840.1.113762.1.4.1219.48",
"meta": {
"versionId": "5",
"lastUpdated": "2023-12-21T17:43:03.000-05:00",
"profile": [
"http://hl7.org/fhir/StructureDefinition/shareablevalueset",
"http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/computable-valueset-cqfm",
"http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/publishable-valueset-cqfm"
]
},
"extension": [
{
"url": "http://hl7.org/fhir/StructureDefinition/valueset-author",
"valueContactDetail": {
"name": "CMS DRLS Author"
}
},
{
"url": "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
"valueDate": "2025-03-03"
},
{
"url": "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
"valueDate": "2022-03-15"
}
],
"url": "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1219.48",
"identifier": [
{
"system": "urn:ietf:rfc:3986",
"value": "urn:oid:2.16.840.1.113762.1.4.1219.48"
}
],
"version": "20220315",
"name": "VentilatorTherapyQualifyingCondition",
"title": "Ventilator Therapy Qualifying Condition",
"status": "active",
"experimental": false,
"date": "2022-03-15T01:04:14-04:00",
"publisher": "CMS DRLS Steward",
"jurisdiction": [
{
"coding": [
{
"system": "urn:iso:std:iso:3166",
"code": "US"
}
]
}
],
"purpose": "(Clinical Focus: Conditions that may qualify a patient to receive ventilator treatment.),(Data Element Scope: Conditions identified by U.S. Centers for Medicare and Medicaid that may justify use of a ventilator.),(Inclusion Criteria: Restrictive lung disease, motor neuron disease, spinal muscular atrophy, chronic respiratory failure, chest wall deformity.),(Exclusion Criteria: No exclusions)",
"compose": {
"include": [
{
"valueSet": [
"http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1219.36"
]
},
{
"valueSet": [
"http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1219.37"
]
},
{
"valueSet": [
"http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1219.42"
]
},
{
"valueSet": [
"http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1219.43"
]
},
{
"valueSet": [
"http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1219.46"
]
},
{
"valueSet": [
"http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1219.45"
]
},
{
"valueSet": [
"http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1219.40"
]
},
{
"valueSet": [
"http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1219.39"
]
}
]
},
"expansion": {
"identifier": "urn:uuid:7df2b748-0e3e-4e31-8866-2ec7ed0b506f",
"timestamp": "2025-05-23T19:43:40-04:00",
"total": 174,
"contains": [
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1003431005",
"display": "Mandibuloacral dysostosis co-occurrent with type A lipodystrophy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1003432003",
"display": "Mandibuloacral dysostosis co-occurrent with type B lipodystrophy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "103851000119100",
"display": "Restrictive lung disease due to amyotrophic lateral sclerosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "103871000119109",
"display": "Restrictive lung disease due to Parkinson disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "10672271000119100",
"display": "Acute-on-chronic hypoxemic respiratory failure (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "10762071000119109",
"display": "Acute-on-chronic respiratory failure following trauma (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "109419009",
"display": "Mandibuloacral dysostosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "111271008",
"display": "Acquired deformity of clavicle (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1172588008",
"display": "Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1172689007",
"display": "Prenatal-onset spinal muscular atrophy with congenital bone fractures (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1197523001",
"display": "Autosomal dominant amyotrophic lateral sclerosis type 1 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1197524007",
"display": "Autosomal recessive amyotrophic lateral sclerosis type 1 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1201863001",
"display": "Amyotrophic lateral sclerosis type 1 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1201947005",
"display": "Juvenile amyotrophic lateral sclerosis type 2 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1201950008",
"display": "Amyotrophic lateral sclerosis type 3 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1201961000",
"display": "Juvenile amyotrophic lateral sclerosis type 5 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1204334005",
"display": "Amyotrophic lateral sclerosis type 6 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1204349002",
"display": "Amyotrophic lateral sclerosis type 7 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1204350002",
"display": "Amyotrophic lateral sclerosis type 8 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1204351003",
"display": "Amyotrophic lateral sclerosis type 9 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1208412003",
"display": "Amyotrophic lateral sclerosis type 10 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1208615009",
"display": "Neurogenic scapuloperoneal syndrome Kaeser type (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "12239621000119103",
"display": "Bells palsy of left side of face (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "12239661000119108",
"display": "Bells palsy of right side of face (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1259121008",
"display": "Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1259122001",
"display": "Amyotrophic lateral sclerosis with parkinsonism (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1259123006",
"display": "Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1259124000",
"display": "Amyotrophic lateral sclerosis with frontotemporal dementia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1259125004",
"display": "Amyotrophic lateral sclerosis with multiple system atrophy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1259126003",
"display": "Amyotrophic lateral sclerosis with autonomic dysfunction (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1259127007",
"display": "Amyotrophic lateral sclerosis with cerebellar dysfunction (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1259129005",
"display": "Amyotrophic lateral sclerosis with spinocerebellar ataxia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1263497002",
"display": "Motor neuron disease due to neoplastic disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1263531001",
"display": "Motor neuron disease due to and following radiotherapy to spinal cord (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1263534009",
"display": "Motor neuron disease due to herpes zoster (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1263535005",
"display": "Motor neuron disease due to human immunodeficiency virus infection (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1263536006",
"display": "Motor neuron disease due to hereditary spastic paraplegia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1263538007",
"display": "Motor neuron disease due to gammopathy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "128212001",
"display": "Spinal muscular atrophy, type II (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "1299151005",
"display": "O'Sullivan McLeod syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "15214001",
"display": "Rachitic rosary (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "15714521000119100",
"display": "Acquired deformity of right rib (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "15714561000119105",
"display": "Acquired deformity of bilateral ribs (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "15714601000119105",
"display": "Acquired deformity of left rib (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "15935701000119103",
"display": "Congenital deformity of left clavicle (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "15935741000119101",
"display": "Congenital deformity of bilateral clavicles (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "15935781000119106",
"display": "Congenital deformity of right clavicle (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "193093009",
"display": "Bell's palsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "20091000175107",
"display": "Acute on chronic hypoxemic and hypercapnic respiratory failure (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "203059008",
"display": "Contracture of pectoralis major (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "205101001",
"display": "Congenital pectus carinatum (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230246005",
"display": "Progressive bulbar palsy of childhood (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230247001",
"display": "Distal spinal muscular atrophy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230248006",
"display": "Scapuloperoneal spinal muscular atrophy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230249003",
"display": "Facioscapulohumeral spinal muscular atrophy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230250003",
"display": "Facioscapulohumeral spinal muscular atrophy with sensory loss (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230251004",
"display": "Scapulohumeral spinal muscular atrophy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230252006",
"display": "Oculopharyngeal spinal muscular atrophy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230253001",
"display": "Bulbospinal neuronopathy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230254007",
"display": "Western Pacific motor neurone disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230255008",
"display": "Madras-type motor neurone disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230257000",
"display": "Paraneoplastic motor neurone disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230258005",
"display": "Amyotrophic lateral sclerosis with dementia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230264003",
"display": "Troyer syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230274000",
"display": "Frontal lobe degeneration with motor neurone disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "230784003",
"display": "Congenital pseudobulbar palsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "24228002",
"display": "Barrel chest (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "249681008",
"display": "Deformity of shaft of clavicle (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "249684000",
"display": "Hooked clavicle (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "249700004",
"display": "Angulation deformity of rib (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "249701000",
"display": "Bowing of rib (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "249704008",
"display": "Flared ribs (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "249892007",
"display": "Progressive pseudobulbar palsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "298727009",
"display": "Deformity of sternum (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "298735007",
"display": "Deformity of rib (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "298736008",
"display": "Notching of ribs (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "305719002",
"display": "Neuromyotonia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "31097004",
"display": "Post poliomyelitis syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "3274008",
"display": "Flat chest (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "350586651000119105",
"display": "Chronic respiratory failure due to neuromuscular disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "35491000119107",
"display": "Restrictive lung mechanics due to neuromuscular disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "36485005",
"display": "Restrictive lung disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "37340000",
"display": "Motor neuron disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "38364001",
"display": "Scorbutic rosary (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "38774000",
"display": "Pectus carinatum (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "391982004",
"display": "Congenital pectus excavatum (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "391986001",
"display": "Acquired pectus excavatum (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "391987005",
"display": "Pectus excavatum (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "398432008",
"display": "Bulbar weakness (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "39871006",
"display": "Chronic respiratory failure (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "426896000",
"display": "Chronic hypercapnic respiratory failure (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "427777003",
"display": "Restrictive lung disease due to muscular dystrophy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "427908002",
"display": "Restrictive lung disease due to kyphoscoliosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "428173007",
"display": "Chronic hypoxemic respiratory failure (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "44395000",
"display": "Spastic tetraplegia with rigidity syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "444693004",
"display": "Pectus deformity of chest (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "448488004",
"display": "Deformity of chest wall (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "449466007",
"display": "Acquired deformity of chest wall (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "45973002",
"display": "Acquired pectus carinatum (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "46251005",
"display": "Corticospinal motor disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "49793008",
"display": "Hereditary motor neuron disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "5262007",
"display": "Spinal muscular atrophy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "54280009",
"display": "Kugelberg-Welander disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "54304004",
"display": "Progressive bulbar palsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "64383006",
"display": "Werdnig-Hoffmann disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "67905004",
"display": "Acute-on-chronic respiratory failure (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "68948008",
"display": "Acquired deformity of rib (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "699866005",
"display": "Progressive bulbar palsy with sensorineural deafness (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "703524005",
"display": "Spinal muscular atrophy with progressive myoclonic epilepsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "711406009",
"display": "Autosomal recessive axonal neuropathy with neuromyotonia (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "715565004",
"display": "Lethal arthrogryposis co-occurrent with anterior horn cell disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "717964007",
"display": "Juvenile primary lateral sclerosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "718555006",
"display": "Juvenile amyotrophic lateral sclerosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "719836007",
"display": "X-linked distal arthrogryposis multiplex congenita (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "721057002",
"display": "Thoracic insufficiency syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "722987009",
"display": "Amyotrophic lateral sclerosis plus syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "723612001",
"display": "Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "733038005",
"display": "Dysmorphism, pectus carinatum, joint laxity syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "7361000175106",
"display": "Acute-on-chronic hypercapnic respiratory failure (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "73671007",
"display": "Scoliotic angulation of ribs (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "7379000",
"display": "Pseudobulbar palsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "75511006",
"display": "Congenital deformity of chest wall (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "763067000",
"display": "Autosomal dominant congenital benign spinal muscular atrophy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "763863002",
"display": "Pectus excavatum, macrocephaly, dysplastic nails syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "766764008",
"display": "X-linked distal spinal muscular atrophy type 3 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "770630005",
"display": "Distal hereditary motor neuropathy type 1 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "770727008",
"display": "Spinal muscular atrophy with respiratory distress type 2 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "771081007",
"display": "Distal hereditary motor neuropathy type 7 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "771238004",
"display": "Spinal atrophy, ophthalmoplegia, pyramidal syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "771302009",
"display": "Autosomal recessive lower motor neuron disease with childhood onset (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "772129007",
"display": "Autosomal dominant childhood-onset proximal spinal muscular atrophy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "782758009",
"display": "Finger hyperphalangy, toe anomalies, severe pectus excavatum syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "783257005",
"display": "Familial recurrent peripheral facial palsy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "783618006",
"display": "Lower motor neuron syndrome with late-adult onset (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "784341001",
"display": "Amyotrophic lateral sclerosis type 4 (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "784391002",
"display": "Autosomal dominant adult-onset proximal spinal muscular atrophy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "785809005",
"display": "Mills syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "7921007",
"display": "Congenital deformity of clavicle (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "81211007",
"display": "Primary lateral sclerosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "838276009",
"display": "Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "84590007",
"display": "Lower motor neuron disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "85505000",
"display": "Adult spinal muscular atrophy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "85672005",
"display": "Anterior horn cell disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "86044005",
"display": "Amyotrophic lateral sclerosis (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "866051002",
"display": "Motor neuron disease due to lead intoxication (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "88923002",
"display": "Progressive muscular atrophy (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "92981007",
"display": "Congenital bent clavicle (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "92988001",
"display": "Congenital bent rib (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "95647008",
"display": "Upper motor neuron disease (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "971918681000119107",
"display": "Chronic respiratory failure due to obstructive sleep apnea (disorder)"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G12.0",
"display": "Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G12.1",
"display": "Other inherited spinal muscular atrophy"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G12.2",
"display": "Motor neuron disease"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G12.20",
"display": "Motor neuron disease, unspecified"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G12.21",
"display": "Amyotrophic lateral sclerosis"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G12.22",
"display": "Progressive bulbar palsy"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G12.23",
"display": "Primary lateral sclerosis"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G12.24",
"display": "Familial motor neuron disease"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G12.25",
"display": "Progressive spinal muscle atrophy"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G12.29",
"display": "Other motor neuron disease"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G12.8",
"display": "Other spinal muscular atrophies and related syndromes"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "G12.9",
"display": "Spinal muscular atrophy, unspecified"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "J96.10",
"display": "Chronic respiratory failure, unspecified whether with hypoxia or hypercapnia"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "J96.11",
"display": "Chronic respiratory failure with hypoxia"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "J96.12",
"display": "Chronic respiratory failure with hypercapnia"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "J96.20",
"display": "Acute and chronic respiratory failure, unspecified whether with hypoxia or hypercapnia"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "J96.21",
"display": "Acute and chronic respiratory failure with hypoxia"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "J96.22",
"display": "Acute and chronic respiratory failure with hypercapnia"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "J96.90",
"display": "Respiratory failure, unspecified, unspecified whether with hypoxia or hypercapnia"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "J96.91",
"display": "Respiratory failure, unspecified with hypoxia"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "J96.92",
"display": "Respiratory failure, unspecified with hypercapnia"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "J98.4",
"display": "Other disorders of lung"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "M95.4",
"display": "Acquired deformity of chest and rib"
},
{
"system": "http://hl7.org/fhir/sid/icd-10-cm",
"version": "2025",
"code": "Q67.8",
"display": "Other congenital deformities of chest"
}
]
}
}
FHIR
FHIRsmith