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
- 40.2.0
- Organisation
- NHSD Primary Care Domain Refsets
- Codelist ID
- nhsd-primary-care-domain-refsets/gdpprmisc_cod
- Version Tag
- 20250627
- Version ID
- 02a21b98
- Number of codes included
- 172
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 |
|---|---|
| 10406007 | Lesch-Nyhan syndrome |
| 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 |
| 1156777001 | Rheumatoid factor positive and cyclic citrullinated peptide antibody negative juvenile polyarthritis |
| 1162462009 | Angelman syndrome due to maternal monosomy 15q11q13 |
| 1172696009 | Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome |
| 1172899000 | Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome |
| 1173024006 | Typical absence seizure |
| 1186711002 | G protein subunit beta 5-related intellectual disability, cardiac arrhythmia syndrome |
| 1186863001 | Arginine vasopressin deficiency due to trauma |
| 1187045009 | Aicardi Goutieres syndrome type 1 |
| 1187046005 | Aicardi Goutieres syndrome type 2 |
| 1187047001 | Aicardi Goutieres syndrome type 3 |
| 1187048006 | Aicardi Goutieres syndrome type 4 |
| 1187049003 | Aicardi Goutieres syndrome type 5 |
| 1208966001 | Generalized onset motor epileptic seizure |
| 1208968000 | Generalized onset atonic epileptic seizure |
| 1208969008 | Generalized onset tonic epileptic seizure |
| 1208970009 | Generalized onset clonic epileptic seizure |
| 1208971008 | Generalized onset myoclonic-atonic epileptic seizure |
| 1208972001 | Generalized onset myoclonic epileptic seizure |
| 1208973006 | Generalized onset myoclonic-tonic-clonic epileptic seizure |
| 1208991001 | Myoclonic epileptic seizure |
| 1217209006 | Generalized onset tonic-clonic epileptic seizure |
| 1236975007 | Behavioral arrest epileptic seizure |
| 1239381000000101 | Haemoglobin E beta plus thalassaemia |
| 1263997005 | Metastatic pilomatrix carcinoma to skin |
| 127067009 | Stress neutrophilia |
| 129639005 | Hereditary neutrophilia |
| 133841000119105 | Merkel cell carcinoma of face |
| 15182000 | Coffin-Lowry syndrome |
| 15285008 | Adenylosuccinate lyase deficiency |
| 16058671000119103 | Transplant rejection of cornea of left eye |
| 16058711000119104 | Transplant failure of cornea of right eye |
| 16058831000119102 | Transplant rejection of cornea of right eye |
| 16058871000119104 | Transplant failure of cornea of left eye |
| 16196000 | Infectious mononucleosis caused by Cytomegalovirus |
| 16294009 | Splenomegaly |
| 165531008 | Lymphocytosis - absolute |
| 16873003 | Musicogenic seizure |
| 16944002 | Mononucleosis syndrome |
| 17122004 | 4p partial monosomy syndrome |
| 184293009 | Patient died at home |
| 184295002 | Patient died in nursing home |
| 184298000 | Patient died in street |
| 19058002 | Congestive splenomegaly |
| 191273000 | Leukemoid reaction of the newborn |
| 191667009 | Paranoid disorder |
| 192981006 | Atonic epileptic seizure |
| 192982004 | Epileptic seizures - akinetic |
| 192991000 | Clonic epileptic seizure |
| 192993002 | Tonic epileptic seizure |
| 19636003 | Monocytosis |
| 205788004 | Fetal alcohol syndrome |
| 230273006 | Frontotemporal degeneration |
| 230447004 | Absence seizure with eyelid myoclonia |
| 230458008 | Atypical absence status epilepticus |
| 234434003 | Alders syndrome |
| 234620006 | Hereditary C1 esterase inhibitor deficiency - dysfunctional factor |
| 23833000 | Poisoning caused by antineoplastic AND/OR immunosuppressive drug |
| 238975005 | Delusion of foul odor |
| 239910001 | Toxic oil syndrome |
| 240789006 | Hepatosplenic schistosomiasis |
| 240790002 | Schistosomal hepatomegaly |
| 240791003 | Hepatic schistosomal granuloma |
| 240792005 | Symmer's pipe-stem fibrosis |
| 240793000 | Schistosomal splenomegaly |
| 246551007 | Absence seizure with automatisms |
| 2593002 | Dubowitz's syndrome |
| 267454002 | Acatalasemia |
| 278484009 | Tropical pulmonary eosinophilia |
| 278855005 | Frontal lobe degeneration |
| 29789008 | Monocytic leukemoid reaction |
| 2990008 | Lymphocytic leukemoid reaction |
| 302823005 | Glucagonoma |
| 302835009 | Pheochromocytoma |
| 304215001 | Patient died during operation |
| 313307000 | Epileptic seizure |
| 313372007 | Patient died in hospice |
| 33301000119105 | Sequela of cardioembolic stroke |
| 33982008 | Hyperphosphatasemia with intellectual disability |
| 37180002 | Chronic nonspecific lung disease |
| 397007003 | Mast cell disorder |
| 403767009 | Acrocephalopolysyndactyly type II |
| 40425004 | Postconcussion syndrome |
| 410796000 | Juvenile seropositive polyarthritis |
| 413150001 | Patient died in general practice premises |
| 41466009 | Myocardial imaging for infarct with ejection fraction, first pass technique |
| 420300004 | New York Heart Association Classification - Class I |
| 420913000 | New York Heart Association Classification - Class III |
| 421460008 | Retinopathy with acquired immunodeficiency syndrome |
| 421704003 | New York Heart Association Classification - Class II |
| 422293003 | New York Heart Association Classification - Class IV |
| 422348008 | Andersen Tawil syndrome |
| 432636005 | Administration of vaccine product containing only Human alphaherpesvirus 3 and Measles morbillivirus and Mumps orthorubulavirus and Rubella virus antigens |
| 433733003 | Administration of second dose of vaccine product containing only Human alphaherpesvirus 3 and Measles morbillivirus and Mumps orthorubulavirus and Rubella virus antigens |
| 449817000 | Peters plus syndrome |
| 45864009 | Senile degeneration of brain |
| 46288008 | Payr's syndrome |
| 47986005 | Genetic anomaly of leukocyte |
| 502521000000103 | [D]Death, not violent/instantaneous |
| 508171000000105 | Severe learning disability |
| 54898003 | Multiple sulfatase deficiency |
| 5619004 | Bardet-Biedl syndrome |
| 56478004 | Leukemoid reaction |
| 572511000119105 | Administration of vaccine product containing only live attenuated Measles morbillivirus and Mumps orthorubulavirus and Rubella virus and Human alphaherpesvirus 3 antigens |
| 59399004 | Cutis laxa, x-linked |
| 613003 | Fragile X syndrome |
| 61596005 | Heterophil-positive mononucleosis syndrome |
| 63119004 | Weaver syndrome |
| 63670007 | Myocardial imaging for infarct, planar technique |
| 64936001 | Löffler's syndrome |
| 65230006 | Heterophil-negative mononucleosis syndrome |
| 67023009 | Lymphocytosis |
| 67155006 | Gerstmann-Straussler-Scheinker syndrome |
| 685101000119106 | Hemoglobin E beta plus thalassemia |
| 698747008 | Patient died in care home |
| 699297004 | Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type |
| 700215003 | Patient died in usual place of residence |
| 7033004 | Absence status epilepticus |
| 70349007 | Pseudoneutrophilia |
| 703535000 | Mowat-Wilson syndrome |
| 710926008 | Periodontitis co-occurrent with familial neutropenia |
| 713742005 | Human immunodeficiency virus antibody detected |
| 71610005 | Neutrophilic leukemoid reaction |
| 716709002 | FRAXE intellectual disability syndrome |
| 71692003 | Leukoerythroblastotic reaction |
| 717223008 | X-linked epilepsy with learning disability and behavior disorder syndrome |
| 719202006 | Spondyloepiphyseal dysplasia tarda Kohn type |
| 719842006 | Congenital hypoplasia of ulna and intellectual disability syndrome |
| 720501007 | Arachnodactyly with abnormal ossification and intellectual disability syndrome |
| 720746006 | Contracture with ectodermal dysplasia and orofacial cleft syndrome |
| 721974000 | Lowry MacLean syndrome |
| 723365002 | Hypotrichosis and intellectual disability syndrome Lopes type |
| 723504000 | Ramos Arroyo syndrome |
| 723621000 | Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome |
| 724137002 | Macrocephaly, obesity, mental disability, ocular abnormality syndrome |
| 724638006 | Splenomegaly co-occurrent and due to storage disease |
| 725589005 | Bullous dystrophy macular type |
| 726672000 | Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome |
| 733088002 | Preaxial polydactyly, colobomata, intellectual disability syndrome |
| 733472005 | Microcephalus, glomerulonephritis, marfanoid habitus syndrome |
| 737081007 | Administration of vaccine product containing only Human alphaherpesvirus 3 antigen for chickenpox |
| 74263009 | Carpenter syndrome |
| 74509007 | Death by cremation |
| 7573000 | Classical phenylketonuria |
| 763618001 | Wiedemann Steiner syndrome |
| 763795006 | Malan overgrowth syndrome |
| 763837007 | Oro-facial digital syndrome type 14 |
| 7689009 | Reading seizure |
| 771471002 | Optic nerve edema, splenomegaly syndrome |
| 773622005 | Craniofacial dysplasia osteopenia syndrome |
| 77527000 | 9p partial trisomy syndrome |
| 783006001 | Low-grade neuroendocrine neoplasm of corpus uteri |
| 783089006 | Macrocephaly, intellectual disability, autism syndrome |
| 792926007 | Armanni-Ebstein kidney due to diabetes mellitus |
| 79631006 | Absence seizure |
| 80369006 | Chronic neutrophilia |
| 80378000 | Neonatal hepatosplenomegaly |
| 83157008 | Fatal familial insomnia |
| 85559002 | Pelger-Huët anomaly |
| 86188000 | Kuru |
| 871909005 | Administration of first dose of vaccine product containing only Human alphaherpesvirus 3 and Measles morbillivirus and Mumps orthorubulavirus and Rubella virus antigens |
| 880529761000119102 | Infection of lower respiratory tract caused by severe acute respiratory syndrome coronavirus 2 |
| 89671000000108 | Patient died in community hospital |
| 931001000000105 | Significant learning disability |
| 95733001 | Eosinophilic keratitis |
| 95892003 | Persistent generalized lymphadenopathy |
| 9740002 | Macroencephaly |
| 984661000000105 | Mild learning disability |
| 984671000000103 | Moderate learning disability |
| 984681000000101 | Profound learning disability |