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
-
Codelist ID
- nhsd-primary-care-domain-refsets/c19misc_cod
-
Version Tag
- 20200812
-
Version ID
- 1d889b9e
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 |
|---|---|
| 10231000132102 | In-vitro fertilization pregnancy |
| 102361000119104 | Chronic pneumonia |
| 10672271000119100 | Acute-on-chronic hypoxemic respiratory failure |
| 10676151000119101 | Mild persistent allergic asthma uncontrolled |
| 10676191000119106 | Mild persistent asthma uncontrolled |
| 10676231000119102 | Mild persistent asthma uncontrolled co-occurrent with allergic rhinitis |
| 10676631000119100 | Moderate persistent allergic asthma uncontrolled |
| 10676671000119102 | Moderate persistent asthma uncontrolled co-occurrent with allergic rhinitis |
| 10676711000119103 | Moderate persistent asthma uncontrolled |
| 10692721000119102 | Chronic obstructive asthma co-occurrent with acute exacerbation of asthma |
| 10692761000119107 | Asthma-chronic obstructive pulmonary disease overlap syndrome |
| 10713006 | Diffuse interstitial rheumatoid disease of lung |
| 10746341000119109 | Acquired immune deficiency syndrome complicating childbirth |
| 10759351000119103 | Sickle cell anemia in mother complicating childbirth |
| 10838971000119103 | Immunodeficiency caused by long term therapeutic use of drug |
| 1095231000000108 | Transplant of kidney using robotic assistance |
| 10964002 | Progressive pulmonary hypertension |
| 1103911000000103 | Severe asthma with fungal sensitisation |
| 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 |
| 111584000 | Reticular dysgenesis |
| 111585004 | Neutropenia associated with autoimmune disease |
| 111936002 | Cerebral sarcoidosis |
| 111937006 | Sarcoidosis, nodular type |
| 11399002 | Pulmonary hypertensive arterial disease |
| 11603001 | Sickle cell retinopathy |
| 117051000119103 | Chronic total occlusion of coronary artery |
| 12240661000119103 | Long term systemic steroid user |
| 12310001 | Childhood bronchiectasis |
| 123772008 | Homozygous hemoglobinopathy |
| 124122005 | Deficiency of 3-hydroxyacyl-CoA dehydrogenase |
| 124166007 | Deficiency of butyryl-CoA dehydrogenase |
| 12428000 | Intrinsic asthma without status asthmaticus |
| 124621004 | Deficiency of enoyl-coenzyme A hydratase |
| 128212001 | Spinal muscular atrophy, type II |
| 128531006 | Islet cell transplant |
| 128596003 | Medium-chain acyl-coenzyme A dehydrogenase deficiency |
| 129452008 | Nonspecific interstitial pneumonia |
| 129642004 | Chronic idiopathic immunoneutropenia in adults |
| 13160009 | Complication of transplanted intestines |
| 13217005 | Fusiform bronchiectasis |
| 13274008 | Atrophic fibrosis of lung |
| 134781000119106 | High risk pregnancy due to recurrent miscarriage |
| 13886001 | Sickle cell nephropathy |
| 15625411000119109 | Long-term current use of apremilast |
| 15625451000119105 | Long-term current use of tofacitinib |
| 15964981000119104 | Congenital anomaly of cardiac chamber |
| 161626009 | History of splenectomy |
| 161665007 | History of renal transplant |
| 161666008 | History of heart recipient |
| 161668009 | History of skin recipient |
| 161669001 | History of bone tissue recipient |
| 161671001 | History of liver recipient |
| 161672008 | History of being lung transplant recipient |
| 16356006 | Multiple pregnancy |
| 169563005 | Pregnant - on history |
| 17363001 | Splenic sarcoidosis |
| 1741000119102 | Intermittent asthma uncontrolled |
| 174425003 | Orthotopic liver transplant |
| 174426002 | Heterotopic liver transplant |
| 174427006 | Replacement of previous liver transplant |
| 174691005 | Transplantation of pancreas and duodenum |
| 174692003 | Whole organ pancreatic transplant |
| 174693008 | Transplantation of tail of pancreas |
| 174694002 | Renewal of transplanted pancreatic tissue |
| 174778000 | Total splenectomy and reimplantation of fragments |
| 174802006 | Allotransplant of heart and lung |
| 174803001 | Revision of transplantation of heart and lung |
| 174808005 | Xenotransplant of heart |
| 174809002 | Heterotopic allotransplant of heart |
| 175901007 | Live donor renal transplant |
| 175902000 | Cadaveric renal transplant |
| 17604001 | Bilateral right-sidedness sequence |
| 18027006 | Transplantation of liver |
| 18354001 | Chronic induration of lung |
| 187233002 | Sarcoidosis of lung with sarcoidosis of lymph nodes |
| 19057007 | Status anginosus |
| 190995003 | Thymic aplasia or dysplasia with immunodeficiency |
| 191001007 | Major histocompatibility complex class I deficiency |
| 191002000 | Major histocompatibility complex class II deficiency |
| 191013002 | Common variable immunodeficiency with autoantibodies to B- or T-cells |
| 192673008 | Sarcoid meningitis |
| 193101001 | Multiple cranial nerve palsies in sarcoidosis |
| 193195000 | Sarcoid neuropathy |
| 19325002 | Traction bronchiectasis |
| 193251003 | Sarcoid myopathy |
| 193370005 | Proliferative retinopathy due to sickle cell disease |
| 195033009 | Sarcoid heart muscle disease |
| 196051003 | Drug-induced interstitial lung disorder |
| 196133001 | Lung disease with systemic sclerosis |
| 196137000 | Lung disease with Sjögren's disease |
| 19682006 | Lupus hepatitis |
| 197368002 | Hepatic granulomas in sarcoidosis |
| 197747000 | Renal tubulo-interstitial disorders in transplant rejection |
| 20091000175107 | Acute on chronic hypoxemic and hypercapnic respiratory failure |
| 203042003 | Myositis in sarcoidosis |
| 204297006 | Total great vessel transposition |
| 206471004 | Perinatal jaundice due to mucoviscidosis |
| 20753005 | Hypertensive heart disease complicating AND/OR reason for care during pregnancy |
| 213148006 | Transplanted organ rejection |
| 213150003 | Kidney transplant failure and rejection |
| 213151004 | Heart transplant failure and rejection |
| 213152006 | Heart-lung transplant failure and rejection |
| 213153001 | Liver transplant failure and rejection |
| 21527007 | Chronic granulomatous disease, type IV |
| 21764004 | Renal carnitine transport defect |
| 21787007 | Sarcoidosis, Darier-Roussy type |
| 22062008 | X-linked glutaric aciduria, type 2 |
| 22482002 | Subacute obliterative bronchiolitis |
| 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 |
| 232033003 | Sickle cell-hemoglobin C retinopathy |
| 232368009 | Nasal sarcoidosis |
| 232458003 | Laryngeal sarcoidosis |
| 232657004 | Single lung transplant |
| 232658009 | Double lung transplant |
| 232659001 | Double lung transplant as a block |
| 232660006 | Bilateral sequential single lung transplant |
| 232973007 | Allotransplant of heart |
| 232974001 | Orthotopic allotransplant of heart |
| 233623000 | Mononuclear interstitial pneumonia |
| 233692000 | Cryptogenic pulmonary eosinophilia |
| 233743002 | Mediastinal lymph node sarcoidosis |
| 233744008 | Hilar lymph node sarcoidosis |
| 233767005 | Stage 1 pulmonary sarcoidosis |
| 233768000 | Stage 2 pulmonary sarcoidosis |
| 233769008 | Stage 3 pulmonary sarcoidosis |
| 233770009 | Stage 4 pulmonary sarcoidosis |
| 233771008 | Endobronchial sarcoidosis |
| 233772001 | Sarcoid pulmonary calcification |
| 233815004 | Persistent pulmonary hypertension of the newborn |
| 233817007 | Triple vessel disease of the heart |
| 233844002 | Accelerated coronary artery disease in transplanted heart |
| 233932001 | Cardiac transplant disorder |
| 233933006 | Cardiac transplant rejection |
| 233934000 | Cardiac transplant failure |
| 233941006 | Solitary pulmonary hypertension |
| 233942004 | Small vessel pulmonary hypertension |
| 233943009 | Sporadic primary pulmonary hypertension |
| 233944003 | Familial primary pulmonary hypertension |
| 233945002 | Pulmonary hypertension caused by drug |
| 233946001 | Large vessel pulmonary hypertension |
| 233947005 | Thromboembolic pulmonary hypertension |
| 233948000 | Post-arteritic pulmonary hypertension |
| 233950008 | Pulmonary hypertension associated with chronic underventilation |
| 233954004 | High altitude pulmonary hypertension |
| 234046009 | Transplant renal vein thrombosis |
| 234336002 | Hemopoietic stem cell transplant |
| 234429002 | Chemotactic disorder |
| 234437005 | Hemophagocytic lymphohistiocytosis |
| 234511009 | Post-splenectomy disorder |
| 234512002 | Post-splenectomy thrombocytosis |
| 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 |
| 234547005 | Combined immunoglobulin G2 and G4 deficiency |
| 234564008 | Primary immunoglobulin catabolism abnormality |
| 234565009 | Immunoglobulin hypercatabolism |
| 234566005 | Familial immunoglobulin hypercatabolism |
| 234587000 | Neutrophil lactoferrin deficiency |
| 234588005 | Neutrophil secondary granule deficiency |
| 235458006 | Exploration of liver transplant |
| 235910007 | Liver transplant disorder |
| 235911006 | Liver transplant rejection |
| 235912004 | Liver transplant failure |
| 235978006 | Cystic fibrosis of pancreas |
| 236138007 | Xenograft renal transplant |
| 236436003 | End stage renal failure with renal transplant |
| 236569000 | Primary non-function of renal transplant |
| 236570004 | Renal transplant rejection |
| 236571000 | Hyperacute rejection of renal transplant |
| 236572007 | Accelerated rejection of renal transplant |
| 236573002 | Very mild acute rejection of renal transplant |
| 236574008 | Acute rejection of renal transplant |
| 236575009 | Acute rejection of renal transplant - grade I |
| 236576005 | Acute rejection of renal transplant - grade II |
| 236577001 | Acute rejection of renal transplant - grade III |
| 236578006 | Chronic rejection of renal transplant |
| 236579003 | Chronic rejection of renal transplant - grade I |
| 236580000 | Chronic rejection of renal transplant - grade II |
| 236581001 | Chronic rejection of renal transplant - grade III |
| 236582008 | Acute-on-chronic rejection of renal transplant |
| 236583003 | Failed renal transplant |
| 236584009 | Perfusion injury of renal transplant |
| 236585005 | De novo transplant disease |
| 236586006 | De novo glomerulonephritis |
| 236587002 | Transplant glomerulopathy |
| 236588007 | Transplant glomerulopathy - early form |
| 236589004 | Transplant glomerulopathy - late form |
| 236610003 | Escape of urine from transplanted ureter |
| 236614007 | Perirenal and periureteric post-transplant lymphocele |
| 237238006 | Pregnancy with uncertain dates |
| 237239003 | Low risk pregnancy |
| 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 |
| 24181002 | Aplasia of thymus gland with immunodeficiency |
| 24369008 | Pulmonary sarcoidosis |
| 24829000 | Eosinophilic ulcerative colitis |
| 24974008 | Myelokathexis |
| 249892007 | Progressive pseudobulbar palsy |
| 25109007 | Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome |
| 253268005 | Abnormal relationship of right ventricle to left ventricle |
| 253276007 | Cor triloculare biventriculare |
| 253287004 | Left sided atrium connecting to right ventricle |
| 253356004 | Left atrial appendage absent |
| 253653004 | Left aortic arch and right descending aorta |
| 253654005 | Right aortic arch and right descending aorta |
| 253718003 | Circumflex runs posterior to pulmonary trunk |
| 253719006 | Circumflex runs posterior to aorta |
| 254067002 | Immuno-osseous dysplasia |
| 25425008 | Autosomal recessive glutaric aciduria, type 2 |
| 254289008 | Post-transplant neoplasia |
| 254290004 | Lymphoproliferative disorder following transplantation |
| 25502009 | Episodic lymphocytopenia |
| 26252007 | Chronic granulomatous disease, type IIA |
| 269295009 | Transplanted organ failure |
| 26950008 | Chronic ectopic atrial tachycardia |
| 27280000 | Liver transplant with recipient hepatectomy |
| 275523003 | Pancytopenia-dysmelia |
| 276367008 | Wanted pregnancy |
| 276517000 | Transient myocardial ischemia of newborn |
| 276518005 | Transient tricuspid regurgitation of newborn |
| 276792008 | Pulmonary hypertension with extreme obesity |
| 276793003 | Pulmonary hypertension with occult mitral stenosis |
| 276794009 | Facultative pulmonary hypertension with shunt at atrial level |
| 277010001 | Unexplained episode of renal transplant dysfunction |
| 277011002 | Pre-existing disease in renal transplant |
| 277451006 | Part organ pancreatic transplant |
| 277656005 | Primary pulmonary hypoplasia |
| 278257006 | Peripheral blood stem cell graft |
| 278928000 | Transient mitral regurgitation of newborn |
| 28009009 | Liver transplant without recipient hepatectomy |
| 281091000 | Ischemic myocardial dysfunction |
| 281093002 | Hibernating myocardium |
| 28122003 | Pulmonary eosinophilic granuloma |
| 282006 | Acute myocardial infarction of basal-lateral wall |
| 28248000 | Left anterior descending coronary artery thrombosis |
| 2829000 | Uhl's disease |
| 286947004 | Chronic rheumatic mitral valve |
| 286950001 | Chronic rheumatic aortic valve disease |
| 287239002 | Thymus transplantation |
| 289317009 | Granulocyte granule deficiency |
| 29272001 | Chronic granulomatous disease, type I |
| 30042003 | Confluent fibrosis of lung |
| 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 |
| 312603000 | Lung transplant rejection |
| 312930008 | Sarcoid chorioretinitis |
| 313030004 | Donor renal transplantation |
| 313039003 | Solid organ transplant |
| 314204000 | Early stage of pregnancy |
| 31541009 | Sarcoidosis |
| 32413006 | Transplantation of heart |
| 32477003 | Heart-lung transplant with recipient cardiectomy-pneumonectomy |
| 328661000119108 | Interstitial lung disease of childhood |
| 33167004 | Complication of transplanted liver |
| 33479006 | Distal subtotal pancreatectomy with splenectomy and pancreaticojejunostomy |
| 34371004 | Subacute obliterative bronchiolitis caused by inhalation of chemical fumes AND/OR vapors |
| 350353007 | De Vaal's syndrome |
| 35037009 | Primary atypical interstitial pneumonia |
| 351287008 | Reticular dysgenesis with congenital aleukocytosis |
| 3514002 | Peribronchial fibrosis of lung |
| 352941000119102 | Sarcoid iridocyclitis |
| 360481003 | Common atrioventricular canal |
| 360573001 | Post-capillary pulmonary hypertension |
| 360578005 | Pulmonary hypertension secondary to raised pulmonary vascular resistance |
| 361197009 | Sarcoid arthropathy |
| 361198004 | Sarcoid arthritis |
| 367542003 | Pulmonary eosinophilia |
| 37061001 | Granulomatous sarcoid nephropathy |
| 37171002 | Abnormal number of leaflets |
| 37340000 | Motor neuron disease |
| 37548006 | Hypopigmentation-immunodeficiency disease |
| 387732009 | Becker muscular dystrophy |
| 387759001 | Chronic granulomatous disease |
| 39041004 | Restrictive cardiomyopathy secondary to sarcoidosis |
| 398250003 | Familial hemophagocytic lymphohistiocytosis |
| 398432008 | Bulbar weakness |
| 39871006 | Chronic respiratory failure |
| 39905002 | Scimitar syndrome |
| 399091004 | Facioscapulohumeral muscular dystrophy |
| 399216004 | D - transposition of the great vessels |
| 40145002 | Congenital neutrophil actin dysfunction |
| 40197009 | Chronic granulomatous disease, type IA |
| 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 |
| 402483002 | Immunodeficiency with multicarboxylase deficiency |
| 402792003 | T-lymphocyte immunodeficiency |
| 403836001 | Autosomal recessive hyperimmunoglobulin M syndrome |
| 403839008 | Siccardi syndrome |
| 405570007 | Pulmonary fibrosis due to and following radiotherapy |
| 408335007 | Autoimmune hepatitis |
| 41371000119100 | Shone complex |
| 415005004 | Panleukopenia |
| 415359008 | Sarcoid uveitis |
| 416729007 | Neutropenia associated with acquired immunodeficiency syndrome |
| 41814009 | Neutropenia with dysgranulopoiesis |
| 41893002 | Left ventricular-right atrial communication |
| 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 |
| 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 |
| 42402006 | Kartagener syndrome |
| 425384007 | Sarcoidosis with glomerulonephritis |
| 425616008 | Transplantation of ileum |
| 425843001 | Allogeneic peripheral blood stem cell transplant |
| 425983008 | Autologous peripheral blood stem cell transplant |
| 426012001 | Right heart failure due to pulmonary hypertension |
| 426136000 | Delayed renal graft function |
| 426356008 | Orthotopic transplantation of whole liver |
| 426463009 | Allotransplantation of ileum |
| 426896000 | Chronic hypercapnic respiratory failure |
| 426984008 | Allotransplantation of thymus gland |
| 427046006 | Drug-induced pneumonitis |
| 427089005 | Diabetes mellitus due to cystic fibrosis |
| 427928003 | Disorder related to lung transplantation |
| 428173007 | Chronic hypoxemic respiratory failure |
| 428198008 | Transplantation of hepatocytes |
| 428575007 | Hypertension secondary to kidney transplant |
| 428645009 | Examination of recipient after kidney transplant |
| 429054002 | Disorder related to transplantation |
| 429257001 | Disorder of transplanted heart |
| 429332008 | Transplantation of single lobe of lung |
| 429451003 | Disorder related to renal transplantation |
| 429490004 | Disorder affecting transplanted structure |
| 431186002 | Accelerated rejection of cardiac transplant |
| 431222008 | Acute rejection of liver transplant |
| 431223003 | Acute rejection of lung transplant |
| 431505005 | Rejection of intestine transplant |
| 431506006 | Rejection of pancreas transplant |
| 431507002 | Accelerated rejection of lung transplant |
| 431896008 | Chronic rejection of cardiac transplant |
| 432772009 | Hyperacute rejection of liver transplant |
| 432773004 | Hyperacute rejection of cardiac transplant |
| 432774005 | Hyperacute rejection of lung transplant |
| 432777003 | Accelerated rejection of liver transplant |
| 432843002 | Acute rejection of cardiac transplant |
| 432908002 | Chronic rejection of liver transplant |
| 432958009 | Chronic rejection of lung transplant |
| 433592008 | Acute rejection of pancreas transplant |
| 433600001 | Hyperacute rejection of intestine transplant |
| 433804007 | Accelerated rejection of intestine transplant |
| 433809002 | Accelerated rejection of pancreas transplant |
| 434202008 | Hyperacute rejection of pancreas transplant |
| 434238001 | Acute rejection of intestine transplant |
| 434270001 | Chronic rejection of intestine transplant |
| 434271002 | Chronic rejection of pancreas transplant |
| 439311009 | Intends to continue pregnancy |
| 441482006 | History of sickle cell anemia |
| 4416007 | Heerfordt's syndrome |
| 44165003 | Complication of transplanted lung |
| 442025000 | Acute exacerbation of chronic asthmatic bronchitis |
| 44395000 | Spastic tetraplegia with rigidity syndrome |
| 444661007 | High risk pregnancy due to history of preterm labor |
| 444855007 | Arteriosclerosis of coronary artery bypass graft of transplanted heart |
| 445237003 | Portopulmonary hypertension |
| 445378003 | Acute exacerbation of bronchiectasis |
| 445928005 | Eisenmenger's syndrome |
| 448975006 | Aortico-left ventricular tunnel with extracardiac aneurysm of aortic wall |
| 44940001 | Adenosine deaminase deficiency |
| 450816007 | Revision of transplantation of heart |
| 45503006 | Common ventricle |
| 459166009 | Dichorionic diamniotic twin pregnancy |
| 459167000 | Monochorionic twin pregnancy |
| 459168005 | Monochorionic diamniotic twin pregnancy |
| 459171002 | Monochorionic monoamniotic twin pregnancy |
| 461359003 | Common coronary artery orifice |
| 46251005 | Corticospinal motor disease |
| 46760003 | Estren-Dameshek anemia |
| 47058000 | Heart transplant with recipient cardiectomy |
| 471851005 | Disorder of myocardium associated with rejection of cardiac transplant |
| 47200007 | High risk pregnancy |
| 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 |
| 473195006 | Normal renal function of transplanted kidney |
| 49793008 | Hereditary motor neuron disease |
| 50196008 | Perialveolar fibrosis of lung |
| 50926003 | Job's syndrome |
| 51068008 | Adult bronchiectasis |
| 52500008 | Saccular bronchiectasis |
| 5262007 | Spinal muscular atrophy |
| 54280009 | Kugelberg-Welander disease |
| 54304004 | Progressive bulbar palsy |
| 54515008 | Sarcoidosis, plaque type |
| 54867000 | Rheumatoid fibrosing alveolitis |
| 5499009 | Pulmonary hypertensive venous disease |
| 55016009 | Congenital muscular hypertrophy-cerebral syndrome |
| 55570000 | Asthma without status asthmaticus |
| 55602000 | Nezelof's syndrome |
| 55941000 | Cutaneous sarcoidosis |
| 56841008 | Massive fibrosis of lung |
| 58797008 | Complication of transplanted kidney |
| 58870009 | Sarcoidosis, anular type |
| 60106004 | Common arterial trunk and separate origin of pulmonary arteries |
| 60194009 | Distal subtotal pancreatectomy with splenectomy |
| 6022005 | Dilated cardiomyopathy secondary to sarcoidosis |
| 60743005 | Purine-nucleoside phosphorylase deficiency |
| 60810003 | Quadruplet pregnancy |
| 61535006 | Transplantation of spleen |
| 61959006 | Common truncus arteriosus |
| 62438007 | Transplantation of pancreas |
| 64254006 | Triplet pregnancy |
| 64383006 | Werdnig-Hoffmann disease |
| 64667001 | Interstitial pneumonia |
| 64757003 | Lymph node sarcoidosis |
| 65147003 | Twin pregnancy |
| 6661000119101 | Coronary arteriosclerosis in native artery of transplanted heart |
| 67562009 | Heterotransplant of pancreas |
| 67682002 | Coronary artery atheroma |
| 67905004 | Acute-on-chronic respiratory failure |
| 68409003 | Organized pneumonia |
| 697896007 | Precapillary pulmonary hypertension |
| 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 |
| 697910001 | Pulmonary hypertension due to lung disease and/or hypoxia |
| 697911002 | Pulmonary hypertension due to chronic obstructive pulmonary disease |
| 697912009 | Pulmonary hypertension due to interstitial lung disease |
| 697913004 | Pulmonary hypertension due to pulmonary disease with mixed restrictive and obstructive pattern |
| 697914005 | Pulmonary hypertension due to sleep-disordered breathing |
| 697915006 | Pulmonary hypertension due to alveolar hypoventilation disorder |
| 697916007 | Pulmonary hypertension due to developmental abnormality of the lung |
| 697917003 | Pulmonary hypertension due to hematological disorder |
| 697918008 | Pulmonary hypertension due to myeloproliferative disorder |
| 697919000 | Pulmonary hypertension due to post-splenectomy hematological disorder |
| 697920006 | Pulmonary hypertension in systemic disorder |
| 697921005 | Pulmonary hypertension in sarcoidosis |
| 697922003 | Pulmonary hypertension in Langerhans cell histiocytosis |
| 697923008 | Pulmonary hypertension in lymphangioleiomyomatosis |
| 697924002 | Pulmonary hypertension in neurofibromatosis |
| 697925001 | Pulmonary hypertension due to systolic systemic ventricular dysfunction |
| 697926000 | Pulmonary hypertension due to diastolic systemic ventricular dysfunction |
| 697927009 | Pulmonary hypertension due to left-sided valvular heart disease |
| 697928004 | Pulmonary venous hypertension due to congenital stenosis of pulmonary vein |
| 698075004 | Syngeneic peripheral blood stem cell transplantation |
| 698296002 | Acute exacerbation of chronic congestive heart failure |
| 698303004 | Awaiting transplantation of bone marrow |
| 698362007 | History of transplantation of pancreas |
| 698367001 | History of transplantation of intestine |
| 698940002 | Arthropathy associated with cystic fibrosis |
| 699866005 | Progressive bulbar palsy with sensorineural deafness |
| 700050004 | Overwhelming infection in asplenic patient |
| 700051000 | Sepsis in asplenic subject |
| 700052007 | Post-splenectomy sepsis |
| 700249006 | Idiopathic interstitial pneumonia |
| 700252003 | Subacute idiopathic pulmonary fibrosis |
| 702343002 | Early onset myopathy with fatal cardiomyopathy |
| 702624008 | Aplasia of spleen |
| 703048006 | Vesicoureteric reflux after renal transplant |
| 703355003 | Pulmonary hypertension due to vasculitis |
| 703523004 | Spondyloenchondrodysplasia with immune dysregulation |
| 703524005 | Spinal muscular atrophy with progressive myoclonic epilepsy |
| 70536003 | Transplant of kidney |
| 707148007 | Recurrent post-transplant renal disease |
| 707152007 | Phagocytic immunodeficiency |
| 707238003 | Sarcoidosis of oral cavity |
| 707418001 | Male infertility due to cystic fibrosis |
| 707419009 | Osteoporosis due to cystic fibrosis |
| 707420003 | Portal hypertension due to cystic fibrosis |
| 707434003 | Pulmonary fibrosis due to Hermansky-Pudlak syndrome |
| 707450006 | Pancreatic insufficiency due to cystic fibrosis of pancreas |
| 707536003 | Digestive system manifestation co-occurrent and due to cystic fibrosis |
| 707542004 | Otorhinolaryngological manifestation co-occurrent and due to cystic fibrosis |
| 70756004 | Bronchial atresia with segmental pulmonary emphysema |
| 707577004 | Female infertility due to cystic fibrosis |
| 707578009 | Perforation of intestine due to cystic fibrosis with meconium ileus |
| 707734002 | Elevated liver enzymes level due to cystic fibrosis |
| 707766007 | Exocrine pancreatic manifestation co-occurrent and due to cystic fibrosis |
| 708026002 | Chronic pneumonitis of infancy |
| 708358003 | Emergency asthma admission since last encounter |
| 7085002 | Hypercalcemia due to sarcoidosis |
| 708537005 | Acute idiopathic pulmonary fibrosis |
| 709115004 | Transplantation of autologous hematopoietic stem cell |
| 709535007 | Periodontitis co-occurrent with infantile genetic agranulocytosis |
| 70995007 | Pulmonary hypertension |
| 710927004 | Periodontitis co-occurrent with cyclical neutropenia |
| 711406009 | Autosomal recessive axonal neuropathy with neuromyotonia |
| 711411006 | Allotransplantation of kidney from beating heart cadaver |
| 711413009 | Allotransplantation of kidney from non-beating heart cadaver |
| 711446003 | Transplantation of kidney regime |
| 711480000 | Activated PI3K-delta syndrome |
| 711483003 | Spinal muscular atrophy with respiratory distress type 1 |
| 713244007 | Drug induced pulmonary fibrosis |
| 713444005 | Hemophagocytic syndrome co-occurrent with human immunodeficiency virus infection |
| 713517003 | Infliximab therapy |
| 713518008 | Mycophenolate therapy |
| 713526000 | Recurrent bacterial pneumonia co-occurrent with human immunodeficiency virus infection |
| 713551004 | Azathioprine therapy |
| 713575004 | Dizygotic twin pregnancy |
| 713576003 | Monozygotic twin pregnancy |
| 713825007 | Renal artery stenosis of transplanted kidney |
| 714153000 | Chronic kidney disease stage 5 with transplant |
| 714203003 | Acute bronchitis co-occurrent with bronchiectasis |
| 715429006 | Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome |
| 715565004 | Lethal arthrogryposis co-occurrent with anterior horn cell disease |
| 716198008 | Growth delay with hydrocephalus and lung hypoplasia syndrome |
| 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 |
| 717964007 | Juvenile primary lateral sclerosis |
| 718107000 | Severe combined immunodeficiency T-cell negative B-cell positive due to janus kinase-3 deficiency |
| 718555006 | Juvenile amyotrophic lateral sclerosis |
| 718572004 | Bethlem myopathy |
| 719218000 | Cryptogenic organizing pneumonia |
| 719456001 | Cleft lip and cleft palate with intestinal malrotation and cardiopathy syndrome |
| 71947008 | Homotransplant of pancreas |
| 719685004 | Absent thumb with short stature and immunodeficiency syndrome |
| 719836007 | X-linked distal arthrogryposis multiplex congenita |
| 720345008 | Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome |
| 720401009 | Cystic fibrosis with gastritis and megaloblastic anemia syndrome |
| 720575002 | Braddock syndrome |
| 720605009 | Cardiac anomaly and heterotaxy syndrome |
| 720853005 | Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome |
| 721095007 | Diaphragmatic defect, limb deficiency, skull defect syndrome |
| 721197001 | Polyneuropathy due to classical cystic fibrosis |
| 721711009 | Autoimmune hepatitis type 1 |
| 721712002 | Autoimmune hepatitis type 2 |
| 721713007 | Autoimmune hepatitis type 3 |
| 721977007 | Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome |
| 722189006 | Abatacept therapy |
| 722288007 | Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome |
| 722987009 | Amyotrophic lateral sclerosis plus syndrome |
| 723308003 | Epidermolysis bullosa simplex with muscular dystrophy |
| 723334006 | Immunodeficiency due to mutation of FAS-associated protein with death domain gene |
| 723512008 | Revesz syndrome |
| 723612001 | Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome |
| 723829000 | Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome |
| 723995003 | Schimke immuno-osseous dysplasia |
| 724159000 | Rituximab therapy |
| 724160005 | Tacrolimus therapy |
| 724165000 | Tofacitinib therapy |
| 724177005 | Ligase 4 syndrome |
| 724275005 | Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency |
| 724276006 | X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome |
| 724500003 | Idiopathic chronic eosinophilic pneumonia |
| 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 |
| 725136003 | Immunodeficiency by defective expression of human leukocyte antigen class 1 |
| 725290000 | Combined immunodeficiency due to partial recombination-activating gene 1 deficiency |
| 725420009 | Congenital muscular dystrophy Paradas type |
| 726021008 | Long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency |
| 726335002 | Common atrioventricular junction |
| 726599006 | Sirolimus therapy |
| 726603006 | Apremilast therapy |
| 72957006 | Diamniotic-monochorionic twins |
| 733453005 | Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome |
| 735433009 | Sarcoidosis of digestive system |
| 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 |
| 735536003 | Adult-onset immunodeficiency |
| 735569003 | Acquired abnormality of atrium |
| 735571003 | Acquired ventricular septal defect |
| 7361000175106 | Acute-on-chronic hypercapnic respiratory failure |
| 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 |
| 73699003 | Common arterial trunk and common origin of pulmonary arteries |
| 737181009 | Interstitial lung disease due to systemic disease |
| 737182002 | Interstitial lung disease due to granulomatous disease |
| 737183007 | Interstitial lung disease due to metabolic disease |
| 737184001 | Interstitial lung disease co-occurrent and due to systemic vasculitis |
| 737295003 | Transplanted kidney present |
| 737296002 | Transplanted lung present |
| 737307003 | Natural-killer cell deficiency |
| 737381004 | World Health Organization 2007 Human immunodeficiency virus infection clinical stage 4 |
| 7379000 | Pseudobulbar palsy |
| 739025007 | Transplanted heart-lung present |
| 74218008 | Coronary artery arising from main pulmonary artery |
| 75403004 | Cardiac sarcoidosis |
| 759761000000102 | Left ventricular outflow tract obstruction due to septal hypertrophy |
| 76077004 | Total pancreatectomy with transplantation |
| 762269004 | Classical cystic fibrosis |
| 762270003 | Atypical cystic fibrosis |
| 76243000 | Chronic granulomatous disease, type IVA |
| 762618008 | Bronchiolitis obliterans syndrome due to and after lung transplantation |
| 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 |
| 765327005 | Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome |
| 765478004 | Allotransplantation of left kidney |
| 765479007 | Allotransplantation of right kidney |
| 76670001 | Duchenne muscular dystrophy |
| 766764008 | X-linked distal spinal muscular atrophy type 3 |
| 766879006 | Combined immunodeficiency due to OX40 deficiency |
| 766983005 | Susceptibility to respiratory infection associated with CD8alpha chain mutation |
| 768556005 | Ataxia pancytopenia syndrome |
| 768560008 | Melanoma differentiation-associated gene 5 deficiency |
| 769167005 | Vaso-occlusive pain co-occurrent and due to sickle cell disease |
| 77097004 | Oculopharyngeal muscular dystrophy |
| 77330006 | Chronic granulomatous disease, type II |
| 78574007 | Hypothyroidism due to sarcoidosis |
| 78643003 | Postcardiotomy syndrome |
| 79369007 | Complication of transplanted pancreas |
| 7990002 | Immunoglobulinemia with isolated somatotropin deficiency |
| 805261000000101 | Bronchiolitis obliterans syndrome after lung transplantation |
| 80941006 | Subcutaneous sarcoidosis |
| 80997009 | Quintuplet pregnancy |
| 81211007 | Primary lateral sclerosis |
| 820361000000105 | Allotransplantation of lobe of lung from live donor |
| 82286005 | Hyperimmunoglobulin M syndrome |
| 82317007 | Chronic granulomatous disease, type III |
| 83457000 | Cylindrical bronchiectasis |
| 843691000000100 | Urological complication of renal transplant |
| 844661000000109 | Vascular complication of renal transplant |
| 84590007 | Lower motor neuron disease |
| 847791000000101 | Rupture of artery of transplanted kidney |
| 847811000000100 | Rupture of vein of transplanted kidney |
| 847881000000107 | Stenosis of vein of transplanted kidney |
| 85081000 | Common arterial trunk and widely separate origin of pulmonary arteries |
| 852981000000100 | Aneurysm of vein of transplanted kidney |
| 853021000000108 | Aneurysm of artery of transplanted kidney |
| 853761000000103 | Living donor liver transplantation |
| 85505000 | Adult spinal muscular atrophy |
| 85672005 | Anterior horn cell disease |
| 86044005 | Amyotrophic lateral sclerosis |
| 864271000000105 | Thrombosis of artery of transplanted kidney |
| 864311000000105 | Thrombosis of vein of transplanted kidney |
| 864471000000106 | Anterior opercular syndrome |
| 866901000000103 | Eosinophilic bronchitis |
| 87394009 | Episodic pulmonary hypertension |
| 87694001 | Pyruvate carboxylase deficiency |
| 88039007 | Transplant of lung |
| 88223008 | Secondary pulmonary hypertension |
| 88923002 | Progressive muscular atrophy |
| 896561000000109 | Transplantation of stomach |
| 896581000000100 | Allotransplantation of stomach |
| 90117007 | Tuberculous fibrosis of lung |
| 90610005 | Interstitial pulmonary fibrosis of prematurity |
| 9105005 | Muscle adenosine monophosphate deaminase deficiency |
| 91259005 | Sarcoidosis, angiolupoid type |
| 928341000000103 | History of heart-lung transplant recipient |
| 9529007 | Sarcoidosis, erythrodermic type |
| 95647008 | Upper motor neuron disease |
| 985971000000106 | Sarcoid vasculitis |
Codes not in the full codelist are in faint grey.