Severely immunocompromised codes
- Coding system
- SNOMED CT
- Coding system release
- unknown
- Organisation
- NHSD Primary Care Domain Refsets
- Codelist ID
- nhsd-primary-care-domain-refsets/sevimatrisk_cod
- Version Tag
- 20211221
- Version ID
- 188bb55f
Versions
- 20211221
Description
Taken from the SEVIMATRISK_COD refset published by NHSD.
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 |
|---|---|
| 111587007 | Severe combined immunodeficiency due to absent interleukin-2 receptor |
| 190993005 | Autosomal recessive severe combined immunodeficiency |
| 190996002 | Severe combined immunodeficiency with reticular dysgenesis |
| 190997006 | Severe combined immunodeficiency with low T- and B-cell numbers |
| 190998001 | Severe combined immunodeficiency with low or normal B-cell numbers |
| 203592006 | X-linked severe combined immunodeficiency |
| 22406001 | Severe combined immunodeficiency due to absent lymphoid stem cells |
| 234437005 | Hemophagocytic lymphohistiocytosis |
| 234557006 | Anti-polysaccharide antibody deficiency |
| 234559009 | Anti-pneumococcal polysaccharide antibody deficiency |
| 234570002 | Severe combined immunodeficiency with maternofetal engraftment |
| 234632005 | Immunodeficiency associated with chromosomal abnormality |
| 234640004 | 18-p syndrome with associated immunodeficiency |
| 234641000 | Immunodeficiency associated with multiple organ system abnormalities |
| 25109007 | Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome |
| 276665006 | Congenital acquired immune deficiency syndrome |
| 31323000 | Severe combined immunodeficiency disease |
| 3439009 | Severe combined immunodeficiency due to absent peripheral T cell maturation |
| 351287008 | Reticular dysgenesis with congenital aleukocytosis |
| 36070007 | Wiskott-Aldrich syndrome |
| 36138009 | Congenital immunodeficiency disease |
| 362993009 | Autosomal recessive severe combined immunodeficiency disease |
| 363040003 | Congenital immunodeficiency involving the hematopoietic system |
| 36980009 | Severe combined immunodeficiency due to absent adenosine deaminase |
| 396330006 | Celiac crisis |
| 396331005 | Celiac disease |
| 398250003 | Familial hemophagocytic lymphohistiocytosis |
| 403837005 | Wiskott-Aldrich autosomal dominant variant syndrome |
| 416729007 | Neutropenia associated with acquired immunodeficiency syndrome |
| 420403001 | Pneumocystosis associated with acquired immunodeficiency syndrome |
| 420544002 | Bacterial pneumonia associated with acquired immunodeficiency syndrome |
| 420787001 | Pneumococcal pneumonia associated with acquired immunodeficiency syndrome |
| 421047005 | Candidiasis of lung associated with acquired immunodeficiency syndrome |
| 421102007 | Aplastic anemia associated with acquired immunodeficiency syndrome |
| 421312009 | Agranulocytosis associated with acquired immunodeficiency syndrome |
| 421508002 | Viral pneumonia associated with acquired immunodeficiency syndrome |
| 421671002 | Pneumonia associated with acquired immunodeficiency syndrome |
| 422003001 | Cachexia associated with acquired immunodeficiency syndrome |
| 426202004 | Immune reconstitution syndrome |
| 442459007 | Combined immunodeficiency disease |
| 44940001 | Adenosine deaminase deficiency |
| 45259000 | Celiac infantilism |
| 45390000 | Severe combined immunodeficiency due to absent interleukin-2 production |
| 49555001 | Severe combined immunodeficiency due to absent T cell receptor |
| 55602000 | Nezelof's syndrome |
| 60743005 | Purine-nucleoside phosphorylase deficiency |
| 61715008 | Celiac disease with diffuse intestinal ulceration |
| 62479008 | Acquired immune deficiency syndrome |
| 713297001 | Candidiasis of esophagus co-occurrent with human immunodeficiency virus infection |
| 715982006 | Severe combined immunodeficiency due to deoxyribonucleic acid cross-link repair protein 1c deficiency |
| 716378008 | Combined immunodeficiency due to Zeta-chain associated protein kinase 70 deficiency |
| 716871006 | Severe combined immunodeficiency due to deoxyribonucleic acid dependent protein kinase catalytic subunit deficiency |
| 717811007 | Combined immunodeficiency due to calcium release activated calcium channel dysfunction |
| 718107000 | Severe combined immunodeficiency T-cell negative B-cell positive due to janus kinase-3 deficiency |
| 71904008 | Severe combined immunodeficiency due to absent class II human leukocyte antigens |
| 720853005 | Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome |
| 722067005 | Severe combined immunodeficiency with hypereosinophilia |
| 722386009 | Celiac disease with epilepsy and cerebral calcification syndrome |
| 724177005 | Ligase 4 syndrome |
| 724641002 | Primary hemophagocytic lymphohistiocytosis |
| 725135004 | Combined immunodeficiency due to CD3gamma deficiency |
| 725290000 | Combined immunodeficiency due to partial recombination-activating gene 1 deficiency |
| 735527002 | Human immunodeficiency virus World Health Organization 2007 stage 4 co-occurrent with tuberculosis |
| 735528007 | Human immunodeficiency virus World Health Organization 2007 stage 4 co-occurrent with malaria |
| 737381004 | World Health Organization 2007 Human immunodeficiency virus infection clinical stage 4 |
| 763623001 | Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency |
| 765145001 | T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency |
| 765188009 | Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency |
| 766879006 | Combined immunodeficiency due to OX40 deficiency |
| 770625006 | Combined immunodeficiency with faciooculoskeletal anomalies syndrome |
| 771479000 | Combined immunodeficiency due to serine/threonine kinase 4 deficiency |
| 771517009 | Severe combined immunodeficiency due to caspase recruitment domain family member 11 deficiency |
| 782751003 | Severe combined immunodeficiency due to inhibitor of nuclear factor kappa B kinase subunit beta deficiency |
| 783617001 | Severe combined immunodeficiency due to lymphocyte-specific protein-tyrosine kinase deficiency |
| 783743009 | Combined immunodeficiency with granulomatosis |
| 784340000 | Combined immunodeficiency due to interleukin 21 receptor deficiency |
Codes not in the full codelist are in faint grey.