Resource ValueSet/FHIR Server from package hl7.fhir.us.covid19library#current (63 ms)

Resources that use this resource

StructureDefinition
covid19-underlying-condition-observation	COVID-19 Underlying Medical Condition observation
underlying-hemoglobinopathy-medical-condition	COVID-19 hemoglobinopathy underlying condition

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	SNOMED CT Canada Immunizations

Narrative

Note: links and images are rebased to the (stated) source

Source

{
  "resourceType" : "ValueSet",
  "id" : "covid91-underlying-hemoglobinopathy-condition-value-set",
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><ul><li>Include these codes as defined in <a href=\"http://www.snomed.org/\"><code>http://snomed.info/sct</code></a><table class=\"none\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td><a href=\"http://snomed.info/id/68913001\">68913001</a></td><td>Alpha thalassemia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/36351005\">36351005</a></td><td>Antithrombin III deficiency (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/306058006\">306058006</a></td><td>Aplastic anemia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/707147002\">707147002</a></td><td>Asplenia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/65959000\">65959000</a></td><td>Beta thalassemia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/64779008\">64779008</a></td><td>Blood coagulation disorder (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/715559004\">715559004</a></td><td>Combined deficiency of factor V and factor VIII (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/767712006\">767712006</a></td><td>Factor IX deficiency (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/4320005\">4320005</a></td><td>Factor V deficiency (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/307091009\">307091009</a></td><td>Factor V Leiden mutation (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/37193007\">37193007</a></td><td>Factor VII deficiency (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/76642003\">76642003</a></td><td>Factor X deficiency (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/767713001\">767713001</a></td><td>Factor XI deficiency (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/359727008\">359727008</a></td><td>Fibrinogen deficiency (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/90935002\">90935002</a></td><td>Hemophilia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/41788008\">41788008</a></td><td>Hereditary factor IX deficiency disease (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/28293008\">28293008</a></td><td>Hereditary factor VIII deficiency disease (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/49762007\">49762007</a></td><td>Hereditary factor XI deficiency disease (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/84828003\">84828003</a></td><td>Leukopenia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/109995007\">109995007</a></td><td>Myelodysplastic syndrome (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/165517008\">165517008</a></td><td>Neutropenia (finding)</td></tr><tr><td><a href=\"http://snomed.info/id/127034005\">127034005</a></td><td>Pancytopenia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/109992005\">109992005</a></td><td>Polycythemia vera (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/76407009\">76407009</a></td><td>Protein C deficiency disease (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/1563006\">1563006</a></td><td>Protein S deficiency disease (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/440989002\">440989002</a></td><td>Prothrombin G20210A mutation (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/127041004\">127041004</a></td><td>Sickle cell-beta-thalassemia (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/127040003\">127040003</a></td><td>Sickle cell-hemoglobin SS disease (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/417357006\">417357006</a></td><td>Sickling disorder due to hemoglobin S (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/302215000\">302215000</a></td><td>Thrombocytopenic disorder (disorder)</td></tr><tr><td><a href=\"http://snomed.info/id/128105004\">128105004</a></td><td>von Willebrand disorder (disorder)</td></tr></table></li></ul></div>"
  },
  "url" : "http://hl7.org/fhir/us/covid19library/ValueSet/covid91-underlying-hemoglobinopathy-condition-value-set",
  "version" : "1.0.0",
  "name" : "COVID19UnderlyingHemoglobinopathyConditionVS",
  "title" : "COVID-19 hemoglobinopathy underlying condition reference set",
  "status" : "active",
  "date" : "2022-07-25T12:22:40+00:00",
  "publisher" : "HL7 International - Clinical Information Modeling Initiative",
  "contact" : [
    {
      "name" : "HL7 International - Clinical Information Modeling Initiative",
      "telecom" : [
        {
          "system" : "url",
          "value" : "http://hl7.org/Special/committees/cimi"
        }
      ]
    },
    {
      "name" : "Logica",
      "telecom" : [
        {
          "system" : "url",
          "value" : "https://www.logicahealth.org/"
        }
      ]
    },
    {
      "name" : "HL7",
      "telecom" : [
        {
          "system" : "url",
          "value" : "https://www.hl7.org"
        }
      ]
    }
  ],
  "description" : "A set of codes that describe underlying hemoglobinopathy conditions for COVID19",
  "jurisdiction" : [
    {
      "coding" : [
        {
          "system" : "urn:iso:std:iso:3166",
          "code" : "US",
          "display" : "United States of America"
        }
      ]
    }
  ],
  "copyright" : "This value set includes content from SNOMED CT, which is copyright © 2002+ International Health Terminology Standards Development Organisation (IHTSDO), and distributed by agreement between IHTSDO and HL7. Implementer use of SNOMED CT is not covered by this agreement",
  "compose" : {
    "include" : [
      {
        "system" : "http://snomed.info/sct",
        "concept" : [
          {
            "code" : "68913001",
            "display" : "Alpha thalassemia (disorder)"
          },
          {
            "code" : "36351005",
            "display" : "Antithrombin III deficiency (disorder)"
          },
          {
            "code" : "306058006",
            "display" : "Aplastic anemia (disorder)"
          },
          {
            "code" : "707147002",
            "display" : "Asplenia (disorder)"
          },
          {
            "code" : "65959000",
            "display" : "Beta thalassemia (disorder)"
          },
          {
            "code" : "64779008",
            "display" : "Blood coagulation disorder (disorder)"
          },
          {
            "code" : "715559004",
            "display" : "Combined deficiency of factor V and factor VIII (disorder)"
          },
          {
            "code" : "767712006",
            "display" : "Factor IX deficiency (disorder)"
          },
          {
            "code" : "4320005",
            "display" : "Factor V deficiency (disorder)"
          },
          {
            "code" : "307091009",
            "display" : "Factor V Leiden mutation (disorder)"
          },
          {
            "code" : "37193007",
            "display" : "Factor VII deficiency (disorder)"
          },
          {
            "code" : "76642003",
            "display" : "Factor X deficiency (disorder)"
          },
          {
            "code" : "767713001",
            "display" : "Factor XI deficiency (disorder)"
          },
          {
            "code" : "359727008",
            "display" : "Fibrinogen deficiency (disorder)"
          },
          {
            "code" : "90935002",
            "display" : "Hemophilia (disorder)"
          },
          {
            "code" : "41788008",
            "display" : "Hereditary factor IX deficiency disease (disorder)"
          },
          {
            "code" : "28293008",
            "display" : "Hereditary factor VIII deficiency disease (disorder)"
          },
          {
            "code" : "49762007",
            "display" : "Hereditary factor XI deficiency disease (disorder)"
          },
          {
            "code" : "84828003",
            "display" : "Leukopenia (disorder)"
          },
          {
            "code" : "109995007",
            "display" : "Myelodysplastic syndrome (disorder)"
          },
          {
            "code" : "165517008",
            "display" : "Neutropenia (finding)"
          },
          {
            "code" : "127034005",
            "display" : "Pancytopenia (disorder)"
          },
          {
            "code" : "109992005",
            "display" : "Polycythemia vera (disorder)"
          },
          {
            "code" : "76407009",
            "display" : "Protein C deficiency disease (disorder)"
          },
          {
            "code" : "1563006",
            "display" : "Protein S deficiency disease (disorder)"
          },
          {
            "code" : "440989002",
            "display" : "Prothrombin G20210A mutation (disorder)"
          },
          {
            "code" : "127041004",
            "display" : "Sickle cell-beta-thalassemia (disorder)"
          },
          {
            "code" : "127040003",
            "display" : "Sickle cell-hemoglobin SS disease (disorder)"
          },
          {
            "code" : "417357006",
            "display" : "Sickling disorder due to hemoglobin S (disorder)"
          },
          {
            "code" : "302215000",
            "display" : "Thrombocytopenic disorder (disorder)"
          },
          {
            "code" : "128105004",
            "display" : "von Willebrand disorder (disorder)"
          }
        ]
      }
    ]
  }
}

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