Logica COVID-19 FHIR Profile Library IG
0.10.1 - CI Build

Logica COVID-19 FHIR Profile Library IG - Local Development build (v0.10.1). See the Directory of published versions

COVID-19 immunocompromised underlying condition reference set

Summary

Defining URL:http://fhir.logicahealth.org/covid19/ValueSet/covid19-underlying-immunocompromised-condition-value-set
Version:0.10.1
Name:COVID19UnderlyingImmunocompromisedConditionVS
Status:Active
Title:COVID-19 immunocompromised underlying condition reference set
Definition:

A set of codes that describe underlying immmunocompromised conditions for COVID19.

Publisher:Logica
Source Resource:XML / JSON / Turtle

References

Content Logical Definition

Logical Definition (CLD)

  • Include these codes as defined in http://snomed.info/sct
    CodeDisplay
    62479008Acquired immune deficiency syndrome (AIDS) (disorder)
    91857003Acute lymphoid leukemia, disease (disorder)
    91861009Acute myeloid leukemia, disease (disorder)
    297279009Administration of steroid (procedure)
    119249001Agammaglobulinemia (finding)
    92814006Chronic lymphoid leukemia, disease (disorder)
    23238000Common variable agammaglobulinemia (disorder)
    234599007Complement 2 deficiency (disorder)
    234600005Complement 4 deficiency (disorder)
    234609006Complement 5 deficiency (disorder)
    234611002Complement 6 deficiency (disorder)
    234612009Complement 7 deficiency (disorder)
    234617003Complement 9 deficiency (disorder)
    771443008Complement component 3 deficiency (disorder)
    24743004Complement deficiency disease (disorder)
    404148006Diffuse large B-cell lymphoma (nodal/systemic with skin involvement) (disorder)
    109965004Diffuse non-Hodgkin's lymphoma, lymphoblastic (disorder)
    308121000Follicular non-Hodgkin's lymphoma (disorder)
    234646005Graft-versus-host disease (disorder)
    118613001Hairy cell leukemia (disorder)
    234336002Hemopoietic stem cell transplant (procedure)
    161651005History of - immunosupressive therapy (situation)
    161648003History of - steroid therapy (situation)
    161663000History of - tissue/organ recipient (situation)
    2631000119108History of bone marrow transplant (situation)
    153351000119102History of peripheral stem cell transplant (situation)
    118599009Hodgkin's disease (disorder)
    86406008Human immunodeficiency virus infection (disorder)
    234532001Immunodeficiency disorder (disorder)
    29260007Immunoglobulin A deficiency (disorder)
    417167007Immunoglobulin deficiency (disorder)
    12631000119106Immunoglobulin G deficiency (disorder)
    86553008Immunosuppressive therapy (procedure)
    449187006Kappa light chain deficiency (disorder)
    277637000Large cell anaplastic lymphoma (disorder)
    93143009Leukemia, disease (disorder)
    302841002Malignant lymphoma - small lymphocytic (disorder)
    93655004Malignant melanoma of skin (disorder)
    428061005Malignant neoplasm of brain (disorder)
    254837009Malignant neoplasm of breast (disorder)
    372062007Malignant neoplasm of central nervous system (disorder)
    781382000Malignant neoplasm of colon and/or rectum (disorder)
    371982006Malignant neoplasm of endocrine gland (disorder)
    187767006Malignant neoplasm of liver and intrahepatic bile ducts (disorder)
    187828007Malignant neoplasm of nasal cavities, middle ear and accessory sinuses (disorder)
    363402007Malignant tumor of esophagus (disorder)
    363461003Malignant tumor of eye (disorder)
    363514001Malignant tumor of female genital organ (disorder)
    363378008Malignant tumor of major salivary gland (disorder)
    363515000Malignant tumor of male genital organ (disorder)
    363497007Malignant tumor of meninges (disorder)
    187692001Malignant tumor of nasopharynx (disorder)
    363392002Malignant tumor of oropharynx (disorder)
    363418001Malignant tumor of pancreas (disorder)
    399068003Malignant tumor of prostate (disorder)
    363509000Malignant tumor of small intestine (disorder)
    363349007Malignant tumor of stomach (disorder)
    363434003Malignant tumor of thymus (disorder)
    363432004Malignant tumor of trachea (disorder)
    118600007Malignant lymphoma (disorder)
    448882009Malignant neoplasm of intraabdominal organ (disorder)
    443487006Mantle cell lymphoma (disorder)
    277622004Mucosa-associated lymphoma (disorder)
    109989006Multiple myeloma (disorder)
    118601006Non-Hodgkin's lymphoma (disorder)
    109371002Overlapping malignant neoplasm of bronchus and lung (disorder)
    109384006Overlapping malignant neoplasm of heart, mediastinum and pleura (disorder)
    109977009Peripheral T-cell lymphoma (disorder)
    444910004Primary mediastinal (thymic) large B-cell lymphoma (disorder)
    93841009Primary malignant neoplasm of intrathoracic organs (disorder)
    110006004Prolymphocytic leukemia (disorder)
    128462008Secondary malignant neoplastic disease (disorder)
    190979003Selective immunoglobulin A deficiency (disorder)
    190980000Selective immunoglobulin M deficiency (disorder)
    31323000Severe combined immunodeficiency disease (disorder)
    313039003Solid organ transplant (procedure)
    88714009Transient hypogammaglobulinemia of infancy (disorder)
    36070007Wiskott-Aldrich syndrome (disorder)

 

Expansion

This value set contains 78 concepts

Expansion based on SNOMED CT International edition 09-Mar 2020

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

CodeDisplayDefinition
62479008Acquired immune deficiency syndrome (AIDS) (disorder)
91857003Acute lymphoid leukemia, disease (disorder)
91861009Acute myeloid leukemia, disease (disorder)
297279009Administration of steroid (procedure)
119249001Agammaglobulinemia (finding)
92814006Chronic lymphoid leukemia, disease (disorder)
23238000Common variable agammaglobulinemia (disorder)
234599007Complement 2 deficiency (disorder)
234600005Complement 4 deficiency (disorder)
234609006Complement 5 deficiency (disorder)
234611002Complement 6 deficiency (disorder)
234612009Complement 7 deficiency (disorder)
234617003Complement 9 deficiency (disorder)
771443008Complement component 3 deficiency (disorder)
24743004Complement deficiency disease (disorder)
404148006Diffuse large B-cell lymphoma (nodal/systemic with skin involvement) (disorder)
109965004Diffuse non-Hodgkin's lymphoma, lymphoblastic (disorder)
308121000Follicular non-Hodgkin's lymphoma (disorder)
234646005Graft-versus-host disease (disorder)
118613001Hairy cell leukemia (disorder)
234336002Hemopoietic stem cell transplant (procedure)
161651005History of - immunosupressive therapy (situation)
161648003History of - steroid therapy (situation)
161663000History of - tissue/organ recipient (situation)
2631000119108History of bone marrow transplant (situation)
153351000119102History of peripheral stem cell transplant (situation)
118599009Hodgkin's disease (disorder)
86406008Human immunodeficiency virus infection (disorder)
234532001Immunodeficiency disorder (disorder)
29260007Immunoglobulin A deficiency (disorder)
417167007Immunoglobulin deficiency (disorder)
12631000119106Immunoglobulin G deficiency (disorder)
86553008Immunosuppressive therapy (procedure)
449187006Kappa light chain deficiency (disorder)
277637000Large cell anaplastic lymphoma (disorder)
93143009Leukemia, disease (disorder)
302841002Malignant lymphoma - small lymphocytic (disorder)
93655004Malignant melanoma of skin (disorder)
428061005Malignant neoplasm of brain (disorder)
254837009Malignant neoplasm of breast (disorder)
372062007Malignant neoplasm of central nervous system (disorder)
781382000Malignant neoplasm of colon and/or rectum (disorder)
371982006Malignant neoplasm of endocrine gland (disorder)
187767006Malignant neoplasm of liver and intrahepatic bile ducts (disorder)
187828007Malignant neoplasm of nasal cavities, middle ear and accessory sinuses (disorder)
363402007Malignant tumor of esophagus (disorder)
363461003Malignant tumor of eye (disorder)
363514001Malignant tumor of female genital organ (disorder)
363378008Malignant tumor of major salivary gland (disorder)
363515000Malignant tumor of male genital organ (disorder)
363497007Malignant tumor of meninges (disorder)
187692001Malignant tumor of nasopharynx (disorder)
363392002Malignant tumor of oropharynx (disorder)
363418001Malignant tumor of pancreas (disorder)
399068003Malignant tumor of prostate (disorder)
363509000Malignant tumor of small intestine (disorder)
363349007Malignant tumor of stomach (disorder)
363434003Malignant tumor of thymus (disorder)
363432004Malignant tumor of trachea (disorder)
118600007Malignant lymphoma (disorder)
448882009Malignant neoplasm of intraabdominal organ (disorder)
443487006Mantle cell lymphoma (disorder)
277622004Mucosa-associated lymphoma (disorder)
109989006Multiple myeloma (disorder)
118601006Non-Hodgkin's lymphoma (disorder)
109371002Overlapping malignant neoplasm of bronchus and lung (disorder)
109384006Overlapping malignant neoplasm of heart, mediastinum and pleura (disorder)
109977009Peripheral T-cell lymphoma (disorder)
444910004Primary mediastinal (thymic) large B-cell lymphoma (disorder)
93841009Primary malignant neoplasm of intrathoracic organs (disorder)
110006004Prolymphocytic leukemia (disorder)
128462008Secondary malignant neoplastic disease (disorder)
190979003Selective immunoglobulin A deficiency (disorder)
190980000Selective immunoglobulin M deficiency (disorder)
31323000Severe combined immunodeficiency disease (disorder)
313039003Solid organ transplant (procedure)
88714009Transient hypogammaglobulinemia of infancy (disorder)
36070007Wiskott-Aldrich syndrome (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