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Packageus.nlm.vsac
Resource TypeValueSet
IdValueSet-2.16.840.1.113883.3.464.1003.113.11.1094.json
FHIR VersionR4
Sourcehttps://vsac.nlm.nih.gov/valueset/2.16.840.1.113883.3.464.1003.113.11.1094/expansion
URLhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.113.11.1094
Version20180310
Statusactive
Date2018-03-10T01:00:08-05:00
NameEhlersDanlosSyndrome
TitleEhlers Danlos Syndrome
Realmus
Authorityhl7
DescriptionFOR 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

ValueSet
2.16.840.1.113883.3.464.1003.113.12.1047Ehlers Danlos Syndrome

Resources that this resource uses

CodeSystem
sctSNOMED codes used in this IG

Narrative

No narrative content found in resource


Source1

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  "meta": {
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    "lastUpdated": "2024-08-12T10:14:58.000-04:00",
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      "valueDate": "2024-02-14"
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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",
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            "code": "10033001",
            "display": "Ehlers-Danlos syndrome, non hydroxylysine deficient ocular type (disorder)"
          },
          {
            "code": "17025000",
            "display": "Ehlers-Danlos syndrome, type 4 (disorder)"
          },
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            "code": "20766005",
            "display": "Ehlers-Danlos syndrome, type 2 (disorder)"
          },
          {
            "code": "25606004",
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          },
          {
            "code": "30652003",
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          },
          {
            "code": "31798004",
            "display": "Corneal fragility keratoglobus, blue sclerae AND joint hypermobility (disorder)"
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          {
            "code": "398114001",
            "display": "Ehlers-Danlos syndrome (disorder)"
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          {
            "code": "4170004",
            "display": "Ehlers-Danlos syndrome, procollagen proteinase resistant (disorder)"
          },
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            "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)"
          }
        ]
      }
    ]
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    "timestamp": "2025-05-23T22:21:24-04:00",
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        "version": "http://snomed.info/sct/731000124108/version/20250301",
        "code": "17025000",
        "display": "Vascular Ehlers-Danlos syndrome (disorder)"
      },
      {
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        "code": "55711009",
        "display": "Arthrochalasia Ehlers-Danlos syndrome (disorder)"
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        "version": "http://snomed.info/sct/731000124108/version/20250301",
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        "display": "Familial articular hypermobility syndrome (disorder)"
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}