COVID-19 FHIR Profile Library IG
0.13.0 - 1st Comment Ballot

This page is part of the Logica COVID-19 FHIR Profile Library IG (v0.13.0: Drafts Ballot 1) based on FHIR R4. The current version which supercedes this version is 1.0.0. For a full list of available versions, see the Directory of published versions

ValueSet: COVID-19 hemoglobinopathy underlying condition reference set

Summary

Defining URL:http://hl7.org/fhir/us/covid19library/ValueSet/covid91-underlying-hemoglobinopathy-condition-value-set
Version:0.13.0
Name:COVID19UnderlyingHemoglobinopathyConditionVS
Title:COVID-19 hemoglobinopathy underlying condition reference set
Status:Active as of 2021-08-27T17:17:04+00:00
Definition:

A set of codes that describe underlying hemoglobinopathy conditions for COVID19

Publisher:HL7 International - Clinical Information Modeling Initiative
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

Source Resource:XML / JSON / Turtle

References

Logical Definition (CLD)

  • Include these codes as defined in 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)

 

Expansion

This value set contains 31 concepts

Expansion based on SNOMED CT United States edition 01-Mar 2021

All codes from system http://snomed.info/sct

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