has_sickle_cell_immuno_def
- Coding system
- SNOMED CT
- Coding system release
- unknown
- Organisation
- QCovid
- Codelist ID
- qcovid/has_sickle_cell_immuno_def
- Version ID
- 1c049d7d
Versions
- 1c049d7d
Description
SNOMED codelist for the has_sickle_cell_immuno_def group in the QCovid® to develop the
COVID-19 Population Risk Assessment.
References
Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.
We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.
| code | term |
|---|---|
| 4434006 | Bloom syndrome (disorder) |
| 9893005 | Immunodeficiency with thymoma (disorder) |
| 23238000 | Common variable agammaglobulinemia (disorder) |
| 24743004 | Complement deficiency disease (disorder) |
| 25472008 | Sickle cell-hemoglobin D disease (disorder) |
| 31323000 | Severe combined immunodeficiency disease (disorder) |
| 35434009 | Sickle cell-hemoglobin C disease (disorder) |
| 36070007 | Wiskott-Aldrich syndrome (disorder) |
| 47986005 | Genetic anomaly of leukocyte (disorder) |
| 50926003 | Job's syndrome (disorder) |
| 65880007 | X-linked agammaglobulinemia (disorder) |
| 88714009 | Transient hypogammaglobulinemia of infancy (disorder) |
| 119249001 | Agammaglobulinemia (finding) |
| 119250001 | Hypogammaglobulinemia (finding) |
| 127040003 | Sickle cell-hemoglobin SS disease (disorder) |
| 127041004 | Sickle cell-beta-thalassemia (disorder) |
| 165816005 | Human immunodeficiency virus positive (finding) |
| 190979003 | Selective immunoglobulin A deficiency (disorder) |
| 190980000 | Selective immunoglobulin M deficiency (disorder) |
| 190981001 | Selective immunoglobulin G deficiency (disorder) |
| 190986006 | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia (finding) |
| 191008001 | Immunodeficiency following hereditary defective response to Epstein-Barr virus (disorder) |
| 191011000 | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions (disorder) |
| 191012007 | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) |
| 191018006 | Lymphocyte function antigen-1 defect (disorder) |
| 193370005 | Proliferative retinopathy due to sickle cell disease (disorder) |
| 234434003 | Alders syndrome (disorder) |
| 234532001 | Immunodeficiency disorder (disorder) |
| 234549008 | Immunoglobulin G4 deficiency (disorder) |
| 234631003 | Immunodeficiency with major anomalies (disorder) |
| 267460002 | Congenital hypogammaglobulinemia (finding) |
| 398055000 | T-lymphocyte deficiency (finding) |
| 398271008 | Predominantly T-cell defect (finding) |
| 414029004 | Disorder of immune function (disorder) |
| 417425009 | Hemoglobin SS disease with crisis (disorder) |
| 426202004 | Immune reconstitution syndrome (disorder) |
| 703538003 | Mannose-binding lectin deficiency (disorder) |
Codes not in the full codelist are in faint grey.