Codes required for COVID-19 pandemic planning and research not included within associated clusters from other services to be returned with no time limit
Metadata
- Coding system
- SNOMED CT (UK Clinical Edition)
- Coding system release
- 39.2.0
- Organisation
- NHSD Primary Care Domain Refsets
- Codelist ID
- nhsd-primary-care-domain-refsets/gdpprmisc_cod
- Version Tag
- 20241205
- Version ID
- 03f68161
- Number of codes included
- 69
About
Description
Taken from the `GDPPRMISC_COD` refset published by NHSD. Contains public sector information licensed under the UK Open Government Licence v3.0 (https://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/).
This codelist was imported automatically. The following codes were not found in the SNOMED CT (UK Clinical Edition) dictionary and so excluded from this codelist: 16649511000001100, 34680411000001107, 35727111000001109, 39566211000001103, 40085011000001101, 16649411000001104, 40085311000001103.
This may be because this codelist contains both clinical terms and medications. In which case you may need to create another codelist for the missing clinical/medication codes.
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 |
|---|---|
| 111684008 | Capsular tear without major disruption of parenchyma of spleen AND with open wound in abdominal cavity |
| 1156774008 | Rheumatoid factor positive and cyclic citrullinated peptide antibody positive juvenile polyarthritis |
| 1172696009 | Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome |
| 1173024006 | Typical absence seizure |
| 1186863001 | Arginine vasopressin deficiency due to trauma |
| 1187045009 | Aicardi Goutieres syndrome type 1 |
| 1187047001 | Aicardi Goutieres syndrome type 3 |
| 1208968000 | Generalized onset atonic epileptic seizure |
| 1208973006 | Generalized onset myoclonic-tonic-clonic epileptic seizure |
| 1217209006 | Generalized onset tonic-clonic epileptic seizure |
| 1236975007 | Behavioral arrest epileptic seizure |
| 129639005 | Hereditary neutrophilia |
| 16058671000119103 | Transplant rejection of cornea of left eye |
| 16058711000119104 | Transplant failure of cornea of right eye |
| 16196000 | Infectious mononucleosis caused by Cytomegalovirus |
| 184295002 | Patient died in nursing home |
| 192982004 | Epileptic seizures - akinetic |
| 192991000 | Clonic epileptic seizure |
| 230273006 | Frontotemporal degeneration |
| 234434003 | Alders syndrome |
| 238975005 | Delusion of foul odor |
| 240790002 | Schistosomal hepatomegaly |
| 240792005 | Symmer's pipe-stem fibrosis |
| 246551007 | Absence seizure with automatisms |
| 267454002 | Acatalasemia |
| 302823005 | Glucagonoma |
| 33301000119105 | Sequela of cardioembolic stroke |
| 403767009 | Acrocephalopolysyndactyly type II |
| 410796000 | Juvenile seropositive polyarthritis |
| 41466009 | Myocardial imaging for infarct with ejection fraction, first pass technique |
| 420913000 | New York Heart Association Classification - Class III |
| 421704003 | New York Heart Association Classification - Class II |
| 422348008 | Andersen Tawil syndrome |
| 45864009 | Senile degeneration of brain |
| 47986005 | Genetic anomaly of leukocyte |
| 508171000000105 | Severe learning disability |
| 56478004 | Leukemoid reaction |
| 61596005 | Heterophil-positive mononucleosis syndrome |
| 63119004 | Weaver syndrome |
| 63670007 | Myocardial imaging for infarct, planar technique |
| 67023009 | Lymphocytosis |
| 699297004 | Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type |
| 7033004 | Absence status epilepticus |
| 70349007 | Pseudoneutrophilia |
| 703535000 | Mowat-Wilson syndrome |
| 710926008 | Periodontitis co-occurrent with familial neutropenia |
| 716709002 | FRAXE intellectual disability syndrome |
| 71692003 | Leukoerythroblastotic reaction |
| 719202006 | Spondyloepiphyseal dysplasia tarda Kohn type |
| 720746006 | Contracture with ectodermal dysplasia and orofacial cleft syndrome |
| 723365002 | Hypotrichosis and intellectual disability syndrome Lopes type |
| 723504000 | Ramos Arroyo syndrome |
| 724137002 | Macrocephaly, obesity, mental disability, ocular abnormality syndrome |
| 724638006 | Splenomegaly co-occurrent and due to storage disease |
| 7573000 | Classical phenylketonuria |
| 763618001 | Wiedemann Steiner syndrome |
| 763795006 | Malan overgrowth syndrome |
| 7689009 | Reading seizure |
| 771471002 | Optic nerve edema, splenomegaly syndrome |
| 773622005 | Craniofacial dysplasia osteopenia syndrome |
| 77527000 | 9p partial trisomy syndrome |
| 792926007 | Armanni-Ebstein kidney due to diabetes mellitus |
| 80369006 | Chronic neutrophilia |
| 80378000 | Neonatal hepatosplenomegaly |
| 880529761000119102 | Infection of lower respiratory tract caused by severe acute respiratory syndrome coronavirus 2 |
| 95733001 | Eosinophilic keratitis |
| 9740002 | Macroencephaly |
| 984671000000103 | Moderate learning disability |
| 984681000000101 | Profound learning disability |