COVID-19 FHIR Profile Library IG Informative Version
1.0.0 - Informative
US
COVID-19 FHIR Profile Library IG Informative Version
1.0.0 - Informative
US
This page is part of the Logica COVID-19 FHIR Profile Library IG (v1.0.0: Informative - Informative) based on FHIR R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions 
| Official URL: http://hl7.org/fhir/us/covid19library/ValueSet/covid91-underlying-hemoglobinopathy-condition-value-set | Version: 1.0.0 | |||
| Active as of 2022-07-25 | Computable Name: COVID19UnderlyingHemoglobinopathyConditionVS | |||
Copyright/Legal: 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 |
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A set of codes that describe underlying hemoglobinopathy conditions for COVID19
References
http://snomed.info/sct| Code | Display |
| 68913001 | Alpha thalassemia (disorder) |
| 36351005 | Antithrombin III deficiency (disorder) |
| 306058006 | Aplastic anemia (disorder) |
| 707147002 | Asplenia (disorder) |
| 65959000 | Beta thalassemia (disorder) |
| 64779008 | Blood coagulation disorder (disorder) |
| 715559004 | Combined deficiency of factor V and factor VIII (disorder) |
| 767712006 | Factor IX deficiency (disorder) |
| 4320005 | Factor V deficiency (disorder) |
| 307091009 | Factor V Leiden mutation (disorder) |
| 37193007 | Factor VII deficiency (disorder) |
| 76642003 | Factor X deficiency (disorder) |
| 767713001 | Factor XI deficiency (disorder) |
| 359727008 | Fibrinogen deficiency (disorder) |
| 90935002 | Hemophilia (disorder) |
| 41788008 | Hereditary factor IX deficiency disease (disorder) |
| 28293008 | Hereditary factor VIII deficiency disease (disorder) |
| 49762007 | Hereditary factor XI deficiency disease (disorder) |
| 84828003 | Leukopenia (disorder) |
| 109995007 | Myelodysplastic syndrome (disorder) |
| 165517008 | Neutropenia (finding) |
| 127034005 | Pancytopenia (disorder) |
| 109992005 | Polycythemia vera (disorder) |
| 76407009 | Protein C deficiency disease (disorder) |
| 1563006 | Protein S deficiency disease (disorder) |
| 440989002 | Prothrombin G20210A mutation (disorder) |
| 127041004 | Sickle cell-beta-thalassemia (disorder) |
| 127040003 | Sickle cell-hemoglobin SS disease (disorder) |
| 417357006 | Sickling disorder due to hemoglobin S (disorder) |
| 302215000 | Thrombocytopenic disorder (disorder) |
| 128105004 | von Willebrand disorder (disorder) |
This value set contains 31 concepts
Expansion based on SNOMED CT United States edition 01-Mar 2022
All codes in this table are from the system http://snomed.info/sct
| Code | Display |
| 68913001 | Alpha thalassemia (disorder) |
| 36351005 | Antithrombin III deficiency (disorder) |
| 306058006 | Aplastic anemia (disorder) |
| 707147002 | Asplenia (disorder) |
| 65959000 | Beta thalassemia (disorder) |
| 64779008 | Blood coagulation disorder (disorder) |
| 715559004 | Combined deficiency of factor V and factor VIII (disorder) |
| 767712006 | Factor IX deficiency (disorder) |
| 4320005 | Factor V deficiency (disorder) |
| 307091009 | Factor V Leiden mutation (disorder) |
| 37193007 | Factor VII deficiency (disorder) |
| 76642003 | Factor X deficiency (disorder) |
| 767713001 | Factor XI deficiency (disorder) |
| 359727008 | Fibrinogen deficiency (disorder) |
| 90935002 | Hemophilia (disorder) |
| 41788008 | Hereditary factor IX deficiency disease (disorder) |
| 28293008 | Hereditary factor VIII deficiency disease (disorder) |
| 49762007 | Hereditary factor XI deficiency disease (disorder) |
| 84828003 | Leukopenia (disorder) |
| 109995007 | Myelodysplastic syndrome (disorder) |
| 165517008 | Neutropenia (finding) |
| 127034005 | Pancytopenia (disorder) |
| 109992005 | Polycythemia vera (disorder) |
| 76407009 | Protein C deficiency disease (disorder) |
| 1563006 | Protein S deficiency disease (disorder) |
| 440989002 | Prothrombin G20210A mutation (disorder) |
| 127041004 | Sickle cell-beta-thalassemia (disorder) |
| 127040003 | Sickle cell-hemoglobin SS disease (disorder) |
| 417357006 | Sickling disorder due to hemoglobin S (disorder) |
| 302215000 | Thrombocytopenic disorder (disorder) |
| 128105004 | von Willebrand disorder (disorder) |
Explanation of the columns that may appear on this page:
| Level | A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies |
| System | The source of the definition of the code (when the value set draws in codes defined elsewhere) |
| Code | The code (used as the code in the resource instance) |
| Display | The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application |
| Definition | An explanation of the meaning of the concept |
| Comments | Additional notes about how to use the code |
IG © 2021+ HL7 International - Clinical Information Modeling Initiative. Package hl7.fhir.us.covid19library#1.0.0 based on FHIR 4.0.1. Generated 2022-07-25
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