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. For a full list of available versions, see the Directory of published versions

ValueSet: COVID-19 hemoglobinopathy underlying condition reference set

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

A set of codes that describe underlying hemoglobinopathy conditions for COVID19

References

Logical Definition (CLD)

 

Expansion

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

CodeDisplay
  68913001Alpha thalassemia (disorder)
  36351005Antithrombin III deficiency (disorder)
  306058006Aplastic anemia (disorder)
  707147002Asplenia (disorder)
  65959000Beta thalassemia (disorder)
  64779008Blood coagulation disorder (disorder)
  715559004Combined deficiency of factor V and factor VIII (disorder)
  767712006Factor IX deficiency (disorder)
  4320005Factor V deficiency (disorder)
  307091009Factor V Leiden mutation (disorder)
  37193007Factor VII deficiency (disorder)
  76642003Factor X deficiency (disorder)
  767713001Factor XI deficiency (disorder)
  359727008Fibrinogen deficiency (disorder)
  90935002Hemophilia (disorder)
  41788008Hereditary factor IX deficiency disease (disorder)
  28293008Hereditary factor VIII deficiency disease (disorder)
  49762007Hereditary factor XI deficiency disease (disorder)
  84828003Leukopenia (disorder)
  109995007Myelodysplastic syndrome (disorder)
  165517008Neutropenia (finding)
  127034005Pancytopenia (disorder)
  109992005Polycythemia vera (disorder)
  76407009Protein C deficiency disease (disorder)
  1563006Protein S deficiency disease (disorder)
  440989002Prothrombin G20210A mutation (disorder)
  127041004Sickle cell-beta-thalassemia (disorder)
  127040003Sickle cell-hemoglobin SS disease (disorder)
  417357006Sickling disorder due to hemoglobin S (disorder)
  302215000Thrombocytopenic disorder (disorder)
  128105004von 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