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Resource ValueSet/FHIR Server from package us.nlm.vsac#0.21.0 (328 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/2.16.840.1.113883.3.526.2.1564/expansion
Url http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.526.2.1564
Version 20220218
Status active
Date 2022-02-18T01:02:19-05:00
Name HereditaryCornealDystrophies
Title Hereditary Corneal Dystrophies
Experimental False
Realm us
Authority hl7
Purpose (Clinical Focus: The purpose of this value set is to represent concepts of a diagnosis of hereditary corneal 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 corneal dystrophies, including congenital, epithelial/juvenile, granular, lattice or macular corneal dystrophies.),(Exclusion Criteria: Excludes concepts that represent a diagnosis for 'unspecified eye.')

Resources that use this resource

ValueSet
http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.526.3.1424 Hereditary Corneal Dystrophies

Resources that this resource uses

CodeSystem
http://snomed.info/sct SNOMED CT (all versions)
http://snomed.info/sct Nutrition Care Process Terminology module
http://snomed.info/sct veri


Source

{
  "resourceType" : "ValueSet",
  "id" : "2.16.840.1.113883.3.526.2.1564",
  "meta" : {
    "versionId" : "45",
    "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" : "2022-02-18"
    }
  ],
  "url" : "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.526.2.1564",
  "identifier" : [
    {
      "system" : "urn:ietf:rfc:3986",
      "value" : "urn:oid:2.16.840.1.113883.3.526.2.1564"
    }
  ],
  "version" : "20220218",
  "name" : "HereditaryCornealDystrophies",
  "title" : "Hereditary Corneal Dystrophies",
  "status" : "active",
  "experimental" : false,
  "date" : "2022-02-18T01:02:19-05:00",
  "publisher" : "American Academy of Ophthalmology Steward",
  "jurisdiction" : [
    {
      "coding" : [
        {
          "system" : "urn:iso:std:iso:3166",
          "code" : "US"
        }
      ]
    }
  ],
  "purpose" : "(Clinical Focus: The purpose of this value set is to represent concepts of a diagnosis of hereditary corneal 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 corneal dystrophies, including congenital, epithelial/juvenile, granular, lattice or macular corneal dystrophies.),(Exclusion Criteria: Excludes concepts that represent a diagnosis for 'unspecified eye.')",
  "compose" : {
    "include" : [
      {
        "system" : "http://snomed.info/sct",
        "concept" : [
          {
            "code" : "129623003",
            "display" : "Iridocorneal endothelial syndrome (disorder)"
          },
          {
            "code" : "1674008",
            "display" : "Juvenile epithelial corneal dystrophy (disorder)"
          },
          {
            "code" : "193837009",
            "display" : "Combined corneal dystrophy (disorder)"
          },
          {
            "code" : "193839007",
            "display" : "Fuchs' corneal dystrophy (disorder)"
          },
          {
            "code" : "231927007",
            "display" : "Fatty degeneration of cornea (disorder)"
          },
          {
            "code" : "231930000",
            "display" : "Reis-Bucklers' corneal dystrophy (disorder)"
          },
          {
            "code" : "231931001",
            "display" : "Stromal corneal dystrophy (disorder)"
          },
          {
            "code" : "231933003",
            "display" : "Lattice corneal dystrophy, isolated form (disorder)"
          },
          {
            "code" : "231934009",
            "display" : "Pre-descemet's corneal dystrophy (disorder)"
          },
          {
            "code" : "29504002",
            "display" : "Posterior polymorphous corneal dystrophy (disorder)"
          },
          {
            "code" : "361199007",
            "display" : "Lattice corneal dystrophy (disorder)"
          },
          {
            "code" : "373426005",
            "display" : "Epithelial basement membrane dystrophy (disorder)"
          },
          {
            "code" : "39662004",
            "display" : "Crystalline corneal dystrophy (disorder)"
          },
          {
            "code" : "397568004",
            "display" : "Granular corneal dystrophy type II (disorder)"
          },
          {
            "code" : "404633004",
            "display" : "Cogan-Reese syndrome (disorder)"
          },
          {
            "code" : "416633008",
            "display" : "Congenital hereditary endothelial dystrophy type 1 (disorder)"
          },
          {
            "code" : "416960004",
            "display" : "Corneal endothelial dystrophy (disorder)"
          },
          {
            "code" : "417065002",
            "display" : "Thiel-Behnke corneal dystrophy (disorder)"
          },
          {
            "code" : "417183007",
            "display" : "Fleck corneal dystrophy (disorder)"
          },
          {
            "code" : "417395001",
            "display" : "Congenital hereditary endothelial dystrophy type 2 (disorder)"
          },
          {
            "code" : "417651000",
            "display" : "Congenital hereditary endothelial dystrophy (disorder)"
          },
          {
            "code" : "418054005",
            "display" : "Macular corneal dystrophy Type I (disorder)"
          },
          {
            "code" : "418435001",
            "display" : "Macular corneal dystrophy Type II (disorder)"
          },
          {
            "code" : "419039007",
            "display" : "Granular corneal dystrophy type I (disorder)"
          },
          {
            "code" : "419197009",
            "display" : "Lattice corneal dystrophy Type I (disorder)"
          },
          {
            "code" : "419395007",
            "display" : "Schnyder crystalline cornea dystrophy (disorder)"
          },
          {
            "code" : "419900000",
            "display" : "Gelatinous droplike corneal dystrophy (disorder)"
          },
          {
            "code" : "430888006",
            "display" : "Dystrophy of anterior cornea (disorder)"
          },
          {
            "code" : "45283008",
            "display" : "Granular corneal dystrophy (disorder)"
          },
          {
            "code" : "5587004",
            "display" : "Corneal dystrophy (disorder)"
          },
          {
            "code" : "60258001",
            "display" : "Macular corneal dystrophy (disorder)"
          },
          {
            "code" : "75663006",
            "display" : "Ring-like corneal dystrophy (disorder)"
          },
          {
            "code" : "77797009",
            "display" : "Hereditary corneal dystrophy (disorder)"
          },
          {
            "code" : "95488001",
            "display" : "Congenital macular corneal dystrophy (disorder)"
          }
        ]
      }
    ]
  },
  "expansion" : {
    "identifier" : "urn:uuid:57d96370-9092-4603-b585-2fed99bbb7b7",
    "timestamp" : "2024-12-10T10:58:23-05:00",
    "total" : 33,
    "contains" : [
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        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "129623003",
        "display" : "Iridocorneal endothelial syndrome (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
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        "display" : "Juvenile epithelial corneal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "193837009",
        "display" : "Combined corneal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "193839007",
        "display" : "Fuchs' corneal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "231927007",
        "display" : "Fatty degeneration of cornea (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "231930000",
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      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "231931001",
        "display" : "Stromal corneal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
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        "display" : "Lattice corneal dystrophy, isolated form (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "231934009",
        "display" : "Pre-descemet's corneal dystrophy (disorder)"
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      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "29504002",
        "display" : "Posterior polymorphous corneal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "361199007",
        "display" : "Lattice corneal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "373426005",
        "display" : "Epithelial basement membrane dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "39662004",
        "display" : "Crystalline corneal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "397568004",
        "display" : "Granular corneal dystrophy type II (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "404633004",
        "display" : "Cogan-Reese syndrome (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "416960004",
        "display" : "Corneal endothelial dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "417065002",
        "display" : "Thiel-Behnke corneal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "417183007",
        "display" : "Fleck corneal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "417395001",
        "display" : "Congenital hereditary endothelial dystrophy type 2 (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "417651000",
        "display" : "Congenital hereditary endothelial dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "418054005",
        "display" : "Macular corneal dystrophy Type I (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "418435001",
        "display" : "Macular corneal dystrophy Type II (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "419039007",
        "display" : "Granular corneal dystrophy type I (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "419197009",
        "display" : "Lattice corneal dystrophy Type I (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "419395007",
        "display" : "Schnyder crystalline cornea dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "419900000",
        "display" : "Gelatinous droplike corneal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "430888006",
        "display" : "Dystrophy of anterior cornea (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "45283008",
        "display" : "Granular corneal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "5587004",
        "display" : "Corneal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "60258001",
        "display" : "Macular corneal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "75663006",
        "display" : "Ring-like corneal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "77797009",
        "display" : "Hereditary corneal dystrophy (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "95488001",
        "display" : "Congenital macular corneal dystrophy (disorder)"
      }
    ]
  },
  "text" : {
  }
}

XIG built as of ??metadata-date??. Found ??metadata-resources?? resources in ??metadata-packages?? packages.