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Resource ValueSet/FHIR Server from package us.nlm.vsac#0.23.0 (109 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/2.16.840.1.113762.1.4.1242.2/expansion
Url http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1242.2
Version 20221014
Status active
Date 2022-10-14T01:02:46-04:00
Name SickleCellDisease
Title Sickle Cell Disease
Experimental False
Realm us
Authority hl7
Purpose (Clinical Focus: The purpose of this value set is to broadly define diagnoses of sickle cell disease (including complications specifically due to sickle cell disease) for use in patient registries, clinical decision support tools, electronic data collection instruments, and analytics.),(Data Element Scope: This value set uses primarily SNOMED CT concepts that full under Top Level Concepts of either 'Clinical finding' or 'Situation with explicit context'.),(Inclusion Criteria: In addition to SS sickle cell anemia, also includes sickle thalassemia, SC disease, and rarer variants. Includes complications specifically due to sickle cell disease (such as Sickle cell arthropathy, Sickle cell retinopathy, etc.).),(Exclusion Criteria: Does not include sickle cell trait alone.)

Resources that use this resource

No resources found

Resources that this resource uses

CodeSystem
http://snomed.info/sct SNOMED CT (all versions)
http://snomed.info/sct SNOMED codes used in this IG
http://snomed.info/sct veri

Source

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        "code" : "763096004",
        "display" : "Disorder of liver due to sickle cell disease (disorder)"
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      {
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        "code" : "769167005",
        "display" : "Vaso-occlusive pain co-occurrent and due to sickle cell disease (disorder)"
      },
      {
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        "code" : "783254003",
        "display" : "Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome (disorder)"
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  "text" : {
  }
}

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