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Resource ValueSet/FHIR Server from package us.nlm.vsac#0.21.0 (141 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/2.16.840.1.113883.3.464.1003.113.12.1044/expansion
Url http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.113.12.1044
Version 20240112
Status active
Date 2024-01-12T01:09:53-05:00
Name OsteogenesisImperfecta
Title Osteogenesis Imperfecta
Experimental False
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 osteogenesis imperfecta.),(Data Element Scope: This value set may use a model element related to Diagnosis.),(Inclusion Criteria: Includes concepts that represent a diagnosis of osteogenesis imperfecta disease including diagnoses in the perinatal population.),(Exclusion Criteria: Excludes concepts that represent a diagnosis of osteoporosis with pseudoglioma.)

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/2.16.840.1.113883.3.464.1003.113.11.1085 Osteogenesis Imperfecta
http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.113.11.1087 Osteogenesis Imperfecta

Source

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  "id" : "2.16.840.1.113883.3.464.1003.113.12.1044",
  "meta" : {
    "versionId" : "13",
    "lastUpdated" : "2024-08-12T12:40:14.000-04:00",
    "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 Institutes for Research Author"
      }
    },
    {
      "url" : "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
      "valueDate" : "2024-01-12"
    },
    {
      "url" : "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
      "valueDate" : "2024-01-12"
    }
  ],
  "url" : "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113883.3.464.1003.113.12.1044",
  "identifier" : [
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      "system" : "urn:ietf:rfc:3986",
      "value" : "urn:oid:2.16.840.1.113883.3.464.1003.113.12.1044"
    }
  ],
  "version" : "20240112",
  "name" : "OsteogenesisImperfecta",
  "title" : "Osteogenesis Imperfecta",
  "status" : "active",
  "date" : "2024-01-12T01:09:53-05:00",
  "publisher" : "American Institutes for Research Steward",
  "description" : "for dxa measure",
  "jurisdiction" : [
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      "coding" : [
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          "system" : "urn:iso:std:iso:3166",
          "code" : "US"
        }
      ]
    }
  ],
  "purpose" : "(Clinical Focus: The purpose of this value set is to represent concepts for a diagnosis of  osteogenesis imperfecta.),(Data Element Scope: This value set may use a model element related to Diagnosis.),(Inclusion Criteria: Includes concepts that represent a diagnosis of osteogenesis imperfecta disease including diagnoses in the perinatal population.),(Exclusion Criteria: Excludes concepts that represent a diagnosis of osteoporosis with pseudoglioma.)",
  "compose" : {
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        ]
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      {
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        ]
      }
    ]
  },
  "expansion" : {
    "identifier" : "urn:uuid:b0fe8329-0346-4e1a-b637-ce94f85901e5",
    "timestamp" : "2024-12-10T10:39:51-05:00",
    "total" : 17,
    "contains" : [
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "1003379004",
        "display" : "Osteogenesis imperfecta type 5 (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "15552004",
        "display" : "Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "205496008",
        "display" : "Osteogenesis imperfecta type II (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "205497004",
        "display" : "Osteogenesis imperfecta type IV (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "254110009",
        "display" : "Osteogenesis imperfecta type IIA (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "254111008",
        "display" : "Osteogenesis imperfecta type IIB (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "254112001",
        "display" : "Osteoporosis with pseudoglioma (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "279309008",
        "display" : "Osteogenesis imperfecta, type IV B (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "280159008",
        "display" : "Osteogenesis imperfecta, type IV A (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "385482004",
        "display" : "Osteogenesis imperfecta type I (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "385483009",
        "display" : "Osteogenesis imperfecta type III (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "63890001",
        "display" : "Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "64404003",
        "display" : "Osteogenesis imperfecta with blue sclerae AND normal teeth (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "7134007",
        "display" : "Osteogenesis imperfecta, dominant perinatal lethal (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "78314001",
        "display" : "Osteogenesis imperfecta (disorder)"
      },
      {
        "system" : "http://snomed.info/sct",
        "version" : "http://snomed.info/sct/731000124108/version/20240901",
        "code" : "86470003",
        "display" : "Osteogenesis imperfecta, recessive perinatal lethal (disorder)"
      },
      {
        "system" : "http://hl7.org/fhir/sid/icd-10-cm",
        "version" : "2025",
        "code" : "Q78.0",
        "display" : "Osteogenesis imperfecta"
      }
    ]
  },
  "text" : {
  }
}

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