FHIR IG analytics
| Package | us.nlm.vsac |
| Resource Type | ValueSet |
| Id | ValueSet-2.16.840.1.113883.3.464.1003.113.11.1094.json |
| FHIR Version | R4 |
| Source | https://vsac.nlm.nih.gov/valueset/2.16.840.1.113883.3.464.1003.113.11.1094/expansion |
| URL | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.113.11.1094 |
| Version | 20180310 |
| Status | active |
| Date | 2018-03-10T01:00:08-05:00 |
| Name | EhlersDanlosSyndrome |
| Title | Ehlers Danlos Syndrome |
| Realm | us |
| Authority | hl7 |
| Description | FOR DXA MEASURE |
| Purpose | (Clinical Focus: The purpose of this value set is to represent concepts for a diagnosis of Ehlers-Danlos syndrome.),(Data Element Scope: This value set may use a model element related to Diagnosis.),(Inclusion Criteria: Includes concepts that represent a diagnosis of Ehlers-Danlos syndrome.),(Exclusion Criteria: No exclusions.) |
Resources that use this resource
Resources that this resource uses
| CodeSystem |
| sct | SNOMED codes used in this IG |
Narrative
No narrative content found in resource
Source1
{
"resourceType": "ValueSet",
"id": "2.16.840.1.113883.3.464.1003.113.11.1094",
"meta": {
"versionId": "5",
"lastUpdated": "2024-08-12T10:14:58.000-04:00",
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"extension": [
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"valueContactDetail": {
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"valueDate": "2024-02-14"
},
{
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"valueDate": "2018-03-10"
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"url": "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.113.11.1094",
"identifier": [
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}
],
"version": "20180310",
"name": "EhlersDanlosSyndrome",
"title": "Ehlers Danlos Syndrome",
"status": "active",
"experimental": false,
"date": "2018-03-10T01:00:08-05:00",
"publisher": "American Institutes for Research Steward",
"description": "FOR DXA MEASURE",
"jurisdiction": [
{
"coding": [
{
"system": "urn:iso:std:iso:3166",
"code": "US"
}
]
}
],
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"compose": {
"include": [
{
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"concept": [
{
"code": "10033001",
"display": "Ehlers-Danlos syndrome, non hydroxylysine deficient ocular type (disorder)"
},
{
"code": "17025000",
"display": "Ehlers-Danlos syndrome, type 4 (disorder)"
},
{
"code": "20766005",
"display": "Ehlers-Danlos syndrome, type 2 (disorder)"
},
{
"code": "25606004",
"display": "Ehlers-Danlos syndrome, hydroxylysine-deficient (disorder)"
},
{
"code": "30652003",
"display": "Ehlers-Danlos syndrome, type 3 (disorder)"
},
{
"code": "31798004",
"display": "Corneal fragility keratoglobus, blue sclerae AND joint hypermobility (disorder)"
},
{
"code": "398114001",
"display": "Ehlers-Danlos syndrome (disorder)"
},
{
"code": "4170004",
"display": "Ehlers-Danlos syndrome, procollagen proteinase resistant (disorder)"
},
{
"code": "50869007",
"display": "Ehlers-Danlos syndrome, type 8 (disorder)"
},
{
"code": "55711009",
"display": "Ehlers-Danlos syndrome, procollagen proteinase deficient (disorder)"
},
{
"code": "59399004",
"display": "Cutis laxa, x-linked (disorder)"
},
{
"code": "67202007",
"display": "Ehlers-Danlos syndrome, type 5 (disorder)"
},
{
"code": "70610001",
"display": "Ehlers-Danlos syndrome, recessive type 4 (disorder)"
},
{
"code": "71322004",
"display": "Ehlers-Danlos syndrome, familial joint laxity type (disorder)"
},
{
"code": "83470009",
"display": "Ehlers-Danlos syndrome, type 1 (disorder)"
},
{
"code": "83586000",
"display": "Ehlers-Danlos syndrome, dysfibronectinemic (disorder)"
},
{
"code": "86667008",
"display": "Ehlers-Danlos syndrome, dominant type 4 (disorder)"
}
]
}
]
},
"expansion": {
"identifier": "urn:uuid:ec33b86a-7f5e-4312-a3fb-057270589231",
"timestamp": "2025-05-23T22:21:24-04:00",
"total": 10,
"contains": [
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "17025000",
"display": "Vascular Ehlers-Danlos syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "25606004",
"display": "Ehlers-Danlos syndrome, hydroxylysine-deficient (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "30652003",
"display": "Hypermobile Ehlers-Danlos syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "398114001",
"display": "Ehlers-Danlos syndrome (disorder)"
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{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "50869007",
"display": "Periodontal Ehlers-Danlos syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "55711009",
"display": "Arthrochalasia Ehlers-Danlos syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "59399004",
"display": "Cutis laxa, x-linked (disorder)"
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{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "67202007",
"display": "X-linked Ehlers-Danlos syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "71322004",
"display": "Familial articular hypermobility syndrome (disorder)"
},
{
"system": "http://snomed.info/sct",
"version": "http://snomed.info/sct/731000124108/version/20250301",
"code": "83586000",
"display": "Ehlers-Danlos syndrome, dysfibronectinemic (disorder)"
}
]
}
}