Codes for conditions raising risk of severe illness from COVID-19 and not included in the clinically vulnerable criteria
Codelist metadata
-
Coding system
- SNOMED CT
-
Coding system release
- unknown
-
Organisation
- NHSD Primary Care Domain Refsets
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Codelist ID
- nhsd-primary-care-domain-refsets/c19misc_cod
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Version Tag
- 20201016
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Version ID
- 1a646465
Versions
About
Description
Taken from the C19MISC_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 |
|---|---|
| 111292008 | Necrotizing sarcoid granulomatosis |
| 111501005 | Congenital hereditary muscular dystrophy |
| 111502003 | Fukuyama congenital muscular dystrophy |
| 111503008 | Merosin deficient congenital muscular dystrophy |
| 111504002 | Walker-Warburg congenital muscular dystrophy |
| 111505001 | Muscle-eye-brain disease, congenital muscular dystrophy |
| 111508004 | Emery-Dreifuss muscular dystrophy |
| 111585004 | Neutropenia associated with autoimmune disease |
| 111936002 | Cerebral sarcoidosis |
| 111937006 | Sarcoidosis, nodular type |
| 11399002 | Pulmonary hypertensive arterial disease |
| 117051000119103 | Chronic total occlusion of coronary artery |
| 12240661000119103 | Long term systemic steroid user |
| 123772008 | Homozygous hemoglobinopathy |
| 124122005 | Deficiency of 3-hydroxyacyl-CoA dehydrogenase |
| 124166007 | Deficiency of butyryl-CoA dehydrogenase |
| 124621004 | Deficiency of enoyl-coenzyme A hydratase |
| 128212001 | Spinal muscular atrophy, type II |
| 128596003 | Medium-chain acyl-coenzyme A dehydrogenase deficiency |
| 129642004 | Chronic idiopathic immunoneutropenia in adults |
| 15625411000119109 | Long-term current use of apremilast |
| 15625451000119105 | Long-term current use of tofacitinib |
| 161669001 | History of bone tissue recipient |
| 17363001 | Splenic sarcoidosis |
| 17604001 | Bilateral right-sidedness sequence |
| 19057007 | Status anginosus |
| 192673008 | Sarcoid meningitis |
| 193101001 | Multiple cranial nerve palsies in sarcoidosis |
| 193195000 | Sarcoid neuropathy |
| 193251003 | Sarcoid myopathy |
| 195033009 | Sarcoid heart muscle disease |
| 19682006 | Lupus hepatitis |
| 197368002 | Hepatic granulomas in sarcoidosis |
| 203042003 | Myositis in sarcoidosis |
| 205615000 | Trisomy 21- meiotic nondisjunction |
| 205616004 | Trisomy 21- mitotic nondisjunction mosaicism |
| 20753005 | Hypertensive heart disease complicating AND/OR reason for care during pregnancy |
| 21764004 | Renal carnitine transport defect |
| 21787007 | Sarcoidosis, Darier-Roussy type |
| 22062008 | X-linked glutaric aciduria, type 2 |
| 22886006 | Glutaric aciduria, type 2 |
| 230193008 | Neurosarcoidosis |
| 230246005 | Progressive bulbar palsy of childhood |
| 230247001 | Distal spinal muscular atrophy |
| 230248006 | Scapuloperoneal spinal muscular atrophy |
| 230249003 | Facioscapulohumeral spinal muscular atrophy |
| 230250003 | Facioscapulohumeral spinal muscular atrophy with sensory loss |
| 230251004 | Scapulohumeral spinal muscular atrophy |
| 230252006 | Oculopharyngeal spinal muscular atrophy |
| 230253001 | Bulbospinal neuronopathy |
| 230254007 | Western Pacific motor neurone disease |
| 230255008 | Madras-type motor neurone disease |
| 230257000 | Paraneoplastic motor neurone disease |
| 230258005 | Amyotrophic lateral sclerosis with dementia |
| 230264003 | Troyer syndrome |
| 230784003 | Congenital pseudobulbar palsy |
| 231799005 | Sarcoid skin of eyelid |
| 232368009 | Nasal sarcoidosis |
| 232458003 | Laryngeal sarcoidosis |
| 233743002 | Mediastinal lymph node sarcoidosis |
| 233744008 | Hilar lymph node sarcoidosis |
| 233817007 | Triple vessel disease of the heart |
| 234513007 | Post-splenectomy leukocytosis |
| 234524009 | Sarcoid dactylitis |
| 234526006 | Ocular sarcoidosis |
| 234527002 | Lacrimal and parotid gland sarcoidosis |
| 234528007 | Nasopharyngeal sarcoidosis |
| 234529004 | Acute sarcoid polymyositis |
| 234530009 | Chronic sarcoid myopathy |
| 234531008 | Orofacial sarcoid |
| 235458006 | Exploration of liver transplant |
| 237997005 | Very long chain acyl-coenzyme A dehydrogenase deficiency |
| 237999008 | Mitochondrial trifunctional protein deficiency |
| 238001003 | Carnitine palmitoyltransferase I deficiency |
| 238002005 | Carnitine palmitoyltransferase II deficiency |
| 238003000 | Carnitine acylcarnitine translocase deficiency |
| 238674006 | Acute skin sarcoidosis |
| 238675007 | Sarcoidosis-induced erythema nodosum |
| 238676008 | Lofgrens syndrome |
| 238677004 | Maculopapular sarcoidosis |
| 238678009 | Chronic skin sarcoidosis |
| 238679001 | Sarcoidosis in scar |
| 238680003 | Papular sarcoidosis |
| 238681004 | Lichenoid sarcoidosis |
| 240047005 | X-linked muscular dystrophy with limb girdle distribution |
| 240048000 | X-linked muscular dystrophy with abnormal dystrophin |
| 240049008 | Intermediate X-linked muscular dystrophy |
| 240050008 | Manifesting female carrier of X-linked muscular dystrophy |
| 240051007 | X-linked limb girdle muscular dystrophy with normal dystrophin |
| 240052000 | Ji muscular dystrophy |
| 240053005 | Hereditary myopathy limited to females |
| 240055003 | Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein |
| 240058001 | Reunion-Indiana Amish type muscular dystrophy |
| 240060004 | Western type of congenital muscular dystrophy |
| 240061000 | Congenital muscular dystrophy with arthrogryposis multiplex congenita |
| 240062007 | Ullrich congenital muscular dystrophy |
| 240063002 | Eichsfeld type congenital muscular dystrophy |
| 240064008 | Hutterite type of muscular dystrophy |
| 240071003 | X-linked muscular dystrophy not predominantly limb girdle |
| 240072005 | Benign scapuloperoneal muscular dystrophy with cardiomyopathy |
| 240073000 | Autosomal recessive muscular dystrophy not predominantly limb girdle |
| 240074006 | Scapulohumeral muscular dystrophy |
| 240075007 | Autosomal dominant muscular dystrophy not predominantly limb girdle |
| 240076008 | Benign scapuloperoneal muscular dystrophy |
| 240078009 | Benign congenital muscular dystrophy with finger flexion contractures |
| 24829000 | Eosinophilic ulcerative colitis |
| 249892007 | Progressive pseudobulbar palsy |
| 253356004 | Left atrial appendage absent |
| 25425008 | Autosomal recessive glutaric aciduria, type 2 |
| 254264002 | Partial trisomy 21 in Down's syndrome |
| 26950008 | Chronic ectopic atrial tachycardia |
| 276517000 | Transient myocardial ischemia of newborn |
| 276518005 | Transient tricuspid regurgitation of newborn |
| 278928000 | Transient mitral regurgitation of newborn |
| 281091000 | Ischemic myocardial dysfunction |
| 281093002 | Hibernating myocardium |
| 282006 | Acute myocardial infarction of basal-lateral wall |
| 28248000 | Left anterior descending coronary artery thrombosis |
| 286947004 | Chronic rheumatic mitral valve |
| 286950001 | Chronic rheumatic aortic valve disease |
| 305719002 | Neuromyotonia |
| 307127004 | Isolated long chain hydroxyacyl-CoA dehydrogenase deficiency |
| 307128009 | Combined long chain hydroxyacyl-coenzyme A dehydrogenase deficiency |
| 307130006 | 3-Ketoacyl-coenzyme A triolase deficiency |
| 308683001 | Transluminal right ventricular biopsy after heart transplant |
| 310607007 | Sarcoidosis of inferior turbinates |
| 31097004 | Post poliomyelitis syndrome |
| 312930008 | Sarcoid chorioretinitis |
| 31541009 | Sarcoidosis |
| 352941000119102 | Sarcoid iridocyclitis |
| 361197009 | Sarcoid arthropathy |
| 361198004 | Sarcoid arthritis |
| 37061001 | Granulomatous sarcoid nephropathy |
| 37340000 | Motor neuron disease |
| 387732009 | Becker muscular dystrophy |
| 39041004 | Restrictive cardiomyopathy secondary to sarcoidosis |
| 398432008 | Bulbar weakness |
| 399091004 | Facioscapulohumeral muscular dystrophy |
| 402368008 | Ichthyosiform sarcoidosis |
| 402369000 | Atrophic sarcoidosis |
| 402370004 | Ulcerative sarcoidosis |
| 402371000 | Verrucous sarcoidosis |
| 402372007 | Subcutaneous nodular sarcoidosis |
| 402373002 | Hypomelanotic sarcoidosis |
| 402374008 | Nail dystrophy due to sarcoidosis |
| 403839008 | Siccardi syndrome |
| 408335007 | Autoimmune hepatitis |
| 41040004 | Complete trisomy 21 syndrome |
| 415359008 | Sarcoid uveitis |
| 421671002 | Pneumonia associated with acquired immunodeficiency syndrome |
| 425384007 | Sarcoidosis with glomerulonephritis |
| 441482006 | History of sickle cell anemia |
| 4416007 | Heerfordt's syndrome |
| 44395000 | Spastic tetraplegia with rigidity syndrome |
| 450816007 | Revision of transplantation of heart |
| 46251005 | Corticospinal motor disease |
| 471851005 | Disorder of myocardium associated with rejection of cardiac transplant |
| 472757001 | Pulmonary venous hypertension as complication of procedure |
| 472758006 | Pulmonary venous hypertension due to compression of pulmonary great vein |
| 472759003 | Pulmonary venous hypertension due to compression of pulmonary great vein by sclerosing mediastinitis |
| 472760008 | Pulmonary venous hypertension due to compression of pulmonary great vein by lymphadenopathy |
| 472761007 | Pulmonary venous hypertension due to compression of pulmonary great vein by neoplasm |
| 472785004 | Right ventricular outflow tract obstruction due to neoplasm |
| 472786003 | Right ventricular outflow tract obstruction due to foreign body |
| 472787007 | Left ventricular outflow tract obstruction due to neoplasm |
| 472790001 | Pulmonary venous hypertension due to disorder of left heart |
| 472803004 | Acquired abnormality of atrioventricular (not morphologically mitral or tricuspid) valve associated with atrioventricular septal defect |
| 49793008 | Hereditary motor neuron disease |
| 5262007 | Spinal muscular atrophy |
| 54280009 | Kugelberg-Welander disease |
| 54304004 | Progressive bulbar palsy |
| 54515008 | Sarcoidosis, plaque type |
| 5499009 | Pulmonary hypertensive venous disease |
| 55016009 | Congenital muscular hypertrophy-cerebral syndrome |
| 55941000 | Cutaneous sarcoidosis |
| 58870009 | Sarcoidosis, anular type |
| 6022005 | Dilated cardiomyopathy secondary to sarcoidosis |
| 64383006 | Werdnig-Hoffmann disease |
| 64757003 | Lymph node sarcoidosis |
| 67682002 | Coronary artery atheroma |
| 697897003 | Heritable pulmonary arterial hypertension |
| 697898008 | Idiopathic pulmonary arterial hypertension |
| 697899000 | Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II mutation |
| 697900005 | Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation |
| 697901009 | Pulmonary arterial hypertension caused by toxin |
| 697902002 | Associated pulmonary arterial hypertension |
| 697903007 | Pulmonary arterial hypertension associated with connective tissue disease |
| 697904001 | Pulmonary arterial hypertension associated with human immunodeficiency virus infection |
| 697906004 | Pulmonary arterial hypertension associated with congenital systemic-to-pulmonary shunt |
| 697907008 | Pulmonary arterial hypertension associated with schistosomiasis |
| 697908003 | Pulmonary arterial hypertension associated with chronic hemolytic anemia |
| 697928004 | Pulmonary venous hypertension due to congenital stenosis of pulmonary vein |
| 698296002 | Acute exacerbation of chronic congestive heart failure |
| 698303004 | Awaiting transplantation of bone marrow |
| 699866005 | Progressive bulbar palsy with sensorineural deafness |
| 702343002 | Early onset myopathy with fatal cardiomyopathy |
| 702624008 | Aplasia of spleen |
| 703524005 | Spinal muscular atrophy with progressive myoclonic epilepsy |
| 707238003 | Sarcoidosis of oral cavity |
| 7085002 | Hypercalcemia due to sarcoidosis |
| 709469005 | Periodontitis co-occurrent with Down syndrome |
| 709535007 | Periodontitis co-occurrent with infantile genetic agranulocytosis |
| 711406009 | Autosomal recessive axonal neuropathy with neuromyotonia |
| 711483003 | Spinal muscular atrophy with respiratory distress type 1 |
| 713517003 | Infliximab therapy |
| 713518008 | Mycophenolate therapy |
| 713551004 | Azathioprine therapy |
| 715429006 | Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome |
| 715565004 | Lethal arthrogryposis co-occurrent with anterior horn cell disease |
| 717964007 | Juvenile primary lateral sclerosis |
| 718555006 | Juvenile amyotrophic lateral sclerosis |
| 718572004 | Bethlem myopathy |
| 719836007 | X-linked distal arthrogryposis multiplex congenita |
| 720575002 | Braddock syndrome |
| 721711009 | Autoimmune hepatitis type 1 |
| 721712002 | Autoimmune hepatitis type 2 |
| 721713007 | Autoimmune hepatitis type 3 |
| 722189006 | Abatacept therapy |
| 722987009 | Amyotrophic lateral sclerosis plus syndrome |
| 723308003 | Epidermolysis bullosa simplex with muscular dystrophy |
| 723612001 | Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome |
| 724159000 | Rituximab therapy |
| 724160005 | Tacrolimus therapy |
| 724165000 | Tofacitinib therapy |
| 724643004 | Transient abnormal myelopoiesis co-occurrent with Down syndrome |
| 724644005 | Myeloid leukemia co-occurrent with Down syndrome |
| 72470008 | Sarcoidosis, lupus pernio type |
| 724780002 | Demyelination of central nervous system co-occurrent and due to neurosarcoidosis |
| 725046003 | Mitochondrial complex I deficiency due to deficiency of acyl-coenzyme A dehydrogenase 9 |
| 725420009 | Congenital muscular dystrophy Paradas type |
| 726021008 | Long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency |
| 726599006 | Sirolimus therapy |
| 726603006 | Apremilast therapy |
| 733194007 | Dementia co-occurrent and due to Down syndrome |
| 735433009 | Sarcoidosis of digestive system |
| 735569003 | Acquired abnormality of atrium |
| 735571003 | Acquired ventricular septal defect |
| 736962007 | Bypass of four or more coronary arteries with prosthesis |
| 736963002 | Bypass of one coronary artery with prosthesis |
| 736964008 | Bypass of three coronary arteries with prosthesis |
| 736965009 | Bypass of two coronary arteries with prosthesis |
| 7379000 | Pseudobulbar palsy |
| 75403004 | Cardiac sarcoidosis |
| 759761000000102 | Left ventricular outflow tract obstruction due to septal hypertrophy |
| 763067000 | Autosomal dominant congenital benign spinal muscular atrophy |
| 763314009 | Congenital muscular dystrophy with hyperlaxity |
| 763533003 | Distal hereditary motor neuropathy Jerash type |
| 764812008 | Autosomal recessive myogenic arthrogryposis multiplex congenita |
| 764944006 | Congenital muscular dystrophy type 1B |
| 765197008 | Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier |
| 76670001 | Duchenne muscular dystrophy |
| 766764008 | X-linked distal spinal muscular atrophy type 3 |
| 77097004 | Oculopharyngeal muscular dystrophy |
| 78574007 | Hypothyroidism due to sarcoidosis |
| 78643003 | Postcardiotomy syndrome |
| 80941006 | Subcutaneous sarcoidosis |
| 81211007 | Primary lateral sclerosis |
| 84590007 | Lower motor neuron disease |
| 85505000 | Adult spinal muscular atrophy |
| 85672005 | Anterior horn cell disease |
| 86044005 | Amyotrophic lateral sclerosis |
| 864471000000106 | Anterior opercular syndrome |
| 87694001 | Pyruvate carboxylase deficiency |
| 88923002 | Progressive muscular atrophy |
| 9105005 | Muscle adenosine monophosphate deaminase deficiency |
| 91259005 | Sarcoidosis, angiolupoid type |
| 9529007 | Sarcoidosis, erythrodermic type |
| 95647008 | Upper motor neuron disease |
| 985971000000106 | Sarcoid vasculitis |
Codes not in the full codelist are in faint grey.