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Resource ValueSet/FHIR Server from package us.nlm.vsac#0.21.0 (94 ms)

Package us.nlm.vsac
Type ValueSet
Id Id
FHIR Version R4
Source http://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113883.3.526.3.1463/expansion
Url http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.526.3.1463
Version 20210219
Status active
Date 2021-02-19T01:00:28-05:00
Name HereditaryRetinalDystrophies
Title Hereditary Retinal Dystrophies
Experimental False
Realm us
Authority hl7
Purpose (Clinical Focus: The purpose of this value set is to represent concepts for diagnoses of hereditary retinal dystrophies.),(Data Element Scope: This value set may use a model element related to Diagnosis.),(Inclusion Criteria: Includes concepts that represent a diagnosis of hereditary retinal or vitreoretinal dystrophies, including Usher syndrome.),(Exclusion Criteria: Excludes concepts that represent a diagnosis for 'unspecified eye.')

Resources that use this resource

No resources found

Resources that this resource uses

CodeSystem
http://snomed.info/sct SNOMED CT (all versions)
http://hl7.org/fhir/sid/icd-10-cm International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM)
http://snomed.info/sct Nutrition Care Process Terminology module
http://snomed.info/sct veri
http://hl7.org/fhir/sid/icd-10-cm International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM)
http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.526.2.1671 Hereditary Retinal Dystrophies
http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.526.2.1673 Hereditary Retinal Dystrophies

Source

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  "id" : "2.16.840.1.113883.3.526.3.1463",
  "meta" : {
    "versionId" : "29",
    "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" : "American Academy of Ophthalmology Author"
      }
    },
    {
      "url" : "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
      "valueDate" : "2024-03-13"
    },
    {
      "url" : "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
      "valueDate" : "2021-02-19"
    }
  ],
  "url" : "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.526.3.1463",
  "identifier" : [
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      "value" : "urn:oid:2.16.840.1.113883.3.526.3.1463"
    }
  ],
  "version" : "20210219",
  "name" : "HereditaryRetinalDystrophies",
  "title" : "Hereditary Retinal Dystrophies",
  "status" : "active",
  "experimental" : false,
  "date" : "2021-02-19T01:00:28-05:00",
  "publisher" : "American Academy of Ophthalmology Steward",
  "jurisdiction" : [
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          "code" : "US"
        }
      ]
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  ],
  "purpose" : "(Clinical Focus: The purpose of this value set is to represent concepts for diagnoses of hereditary retinal dystrophies.),(Data Element Scope: This value set may use a model element related to Diagnosis.),(Inclusion Criteria: Includes concepts that represent a diagnosis of hereditary retinal or vitreoretinal dystrophies, including Usher syndrome.),(Exclusion Criteria: Excludes concepts that represent a diagnosis for 'unspecified eye.')",
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  "expansion" : {
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    "timestamp" : "2024-12-10T11:09:45-05:00",
    "total" : 25,
    "contains" : [
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "15059000",
        "display" : "Retinal dystrophy in systemic lipidosis (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "192788009",
        "display" : "Retinal dystrophy in cerebroretinal lipidosis (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "193400007",
        "display" : "Hereditary retinal dystrophies in lipidoses (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "193409008",
        "display" : "Hyaline retinal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "193415008",
        "display" : "Tapetoretinal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "232052009",
        "display" : "Autosomal dominant retinitis pigmentosa (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "232053004",
        "display" : "Autosomal recessive retinitis pigmentosa (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "232056007",
        "display" : "Progressive rod dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "232057003",
        "display" : "Usher syndrome type 1 (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "232058008",
        "display" : "Usher syndrome type 2 (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "267613004",
        "display" : "Progressive cone dystrophy (without rod involvement) (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "28835009",
        "display" : "Retinitis pigmentosa (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "312917007",
        "display" : "Cone dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "313003009",
        "display" : "Rod dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "41799005",
        "display" : "Hereditary retinal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "57838006",
        "display" : "Retinitis pigmentosa-deafness syndrome (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "764939004",
        "display" : "Fundus albipunctatus (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "79556007",
        "display" : "Vitreoretinal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "80328002",
        "display" : "Progressive cone-rod dystrophy (disorder)"
      },
      {
        "system" : "http://hl7.org/fhir/sid/icd-10-cm",
        "version" : "2025",
        "code" : "H35.50",
        "display" : "Unspecified hereditary retinal dystrophy"
      },
      {
        "system" : "http://hl7.org/fhir/sid/icd-10-cm",
        "version" : "2025",
        "code" : "H35.51",
        "display" : "Vitreoretinal dystrophy"
      },
      {
        "system" : "http://hl7.org/fhir/sid/icd-10-cm",
        "version" : "2025",
        "code" : "H35.52",
        "display" : "Pigmentary retinal dystrophy"
      },
      {
        "system" : "http://hl7.org/fhir/sid/icd-10-cm",
        "version" : "2025",
        "code" : "H35.53",
        "display" : "Other dystrophies primarily involving the sensory retina"
      },
      {
        "system" : "http://hl7.org/fhir/sid/icd-10-cm",
        "version" : "2025",
        "code" : "H35.54",
        "display" : "Dystrophies primarily involving the retinal pigment epithelium"
      },
      {
        "system" : "http://hl7.org/fhir/sid/icd-10-cm",
        "version" : "2025",
        "code" : "H36.89",
        "display" : "Other retinal disorders in diseases classified elsewhere"
      }
    ]
  },
  "text" : {
  }
}

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