{ "description": "A set of codes that describe underlying hemoglobinopathy conditions for COVID19", "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)" } ] } ] }, "_filename": "ValueSet-covid91-underlying-hemoglobinopathy-condition-value-set.json", "package_name": "hl7.fhir.us.covid19library", "date": "2022-07-25T13:21:55+00:00", "publisher": "HL7 International - Clinical Information Modeling Initiative", "jurisdiction": [ { "coding": [ { "code": "US", "system": "urn:iso:std:iso:3166", "display": "United States of America" } ] } ], "name": "COVID19UnderlyingHemoglobinopathyConditionVS", "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", "type": null, "experimental": null, "resourceType": "ValueSet", "title": "COVID-19 hemoglobinopathy underlying condition reference set", "package_version": "1.0.0", "status": "active", "id": "cb35a8ff-187b-4f54-b63f-51ce2871915b", "kind": null, "url": "http://hl7.org/fhir/us/covid19library/ValueSet/covid91-underlying-hemoglobinopathy-condition-value-set", "version": "1.0.0", "contact": [ { "name": "HL7 International - Clinical Information Modeling Initiative", "telecom": [ { "value": "http://hl7.org/Special/committees/cimi", "system": "url" } ] }, { "name": "Logica", "telecom": [ { "value": "https://www.logicahealth.org/", "system": "url" } ] }, { "name": "HL7", "telecom": [ { "value": "https://www.hl7.org", "system": "url" } ] } ] }