Chronic Liver disease codes
Codelist metadata
-
Coding system
- SNOMED CT
-
Coding system release
- 36.0.0
-
Organisation
- PRIMIS Covid Vaccination Uptake Reporting
-
Codelist ID
- primis-covid19-vacc-uptake/cld
-
Version Tag
- v2.5
-
Version ID
- 2386d8f6
Versions
About
Description
Taken from the CLD_COD field in SARS-CoV2 COVID19 Vaccination Uptake Reporting Codes 20_21 v1, published by PRIMIS.
© PRIMIS - the University of Nottingham 2021
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 |
|---|---|
| 1003567000 | Agenesis of bile duct |
| 1010616001 | Cirrhosis of liver due to classical cystic fibrosis |
| 10295004 | Chronic viral hepatitis |
| 103611000119102 | Cirrhosis of liver due to hepatitis B |
| 10690671000119109 | Stage 3 hepatic fibrosis |
| 1092801000119102 | Hepatic ascites co-occurrent with chronic active hepatitis due to toxic liver disease |
| 109819003 | Obstructive biliary cirrhosis |
| 1116000 | Chronic aggressive type B viral hepatitis |
| 11179002 | Glycogen storage disease, type IV |
| 111891008 | Viral hepatitis B without hepatic coma |
| 1137357005 | Hepatic coma due to viral hepatitis D |
| 1148573000 | Hepatic failure following surgical procedure |
| 1155841005 | Progressive familial intrahepatic cholestasis type 2 |
| 1155913007 | Progressive familial intrahepatic cholestasis type 1 |
| 1162916008 | Glycogen storage disease due to muscle beta-enolase deficiency |
| 1186809004 | Glycogen storage disease due to lactate dehydrogenase deficiency |
| 1186865008 | Progressive familial intrahepatic cholestasis type 3 |
| 1187461004 | Glycogen storage disease due to aldolase A deficiency |
| 1187462006 | Glycogen storage disease due to phosphoglycerate kinase 1 deficiency |
| 1197150002 | Recurrent hepatitis C virus induced liver disease following liver transplant |
| 1197664001 | Secondary portal hypertension |
| 1197704005 | Autoantibody negative autoimmune hepatitis |
| 1197736003 | Chronic hepatic failure due to portosystemic shunt |
| 1197739005 | Hepatic fibrosis due to non-alcoholic fatty liver disease |
| 1220580006 | Isolated neonatal sclerosing cholangitis |
| 12224501000119108 | Infection of transplanted liver |
| 1228849007 | Polyglucosan body myopathy type 2 |
| 1230291009 | Primary biliary cholangitis and/or primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome |
| 1230303001 | Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease |
| 1230342001 | Hepatitis B reinfection following transplantation of liver |
| 1234778004 | Steatohepatitis caused by ethanol |
| 1234822009 | Idiopathic ductopenia |
| 123604002 | Toxic cirrhosis |
| 123605001 | Nutritional cirrhosis |
| 123606000 | Cholangiolitic cirrhosis |
| 123607009 | Septal fibrosis of liver |
| 12368000 | Secondary biliary cirrhosis |
| 123716002 | Latent cirrhosis |
| 123717006 | Advanced cirrhosis |
| 1237346001 | Caroli syndrome |
| 125921000119106 | Hepatic coma due to acute hepatitis C |
| 1260140008 | Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome |
| 128241005 | Inflammatory disease of liver |
| 128302006 | Chronic hepatitis C |
| 1287007 | Congenital absence of bile duct |
| 146371000119104 | Hepatic coma due to chronic hepatitis C |
| 1512006 | Congenital stricture of bile duct |
| 153091000119109 | Hepatic coma due to chronic hepatitis B with delta agent |
| 154211000119108 | Chronic pancreatitis due to chronic alcoholism |
| 15978003 | Glycogen storage disease, muscular form |
| 15999000 | Mixed micro and macronodular cirrhosis |
| 16060001 | Hepatic coma due to viral hepatitis A |
| 16070004 | Syphilitic cirrhosis |
| 16098491000119109 | Chronic autoimmune hepatitis |
| 174425003 | Orthotopic liver transplant |
| 174426002 | Heterotopic liver transplant |
| 174427006 | Replacement of previous liver transplant |
| 1761006 | Biliary cirrhosis |
| 18027006 | Transplantation of liver |
| 186273003 | Tuberculosis of liver |
| 186624004 | Hepatic coma due to acute hepatitis B with delta agent |
| 186626002 | Acute hepatitis B with delta-agent (coinfection) without hepatic coma |
| 186628001 | Hepatic coma due to viral hepatitis C |
| 186639003 | Chronic viral hepatitis B without delta-agent |
| 190823004 | Westphal-Strumpell syndrome |
| 190944000 | Alpha-1-antitrypsin hepatitis |
| 192008 | Congenital syphilitic hepatomegaly |
| 195025008 | Cardiac glycogenosis |
| 19682006 | Lupus hepatitis |
| 197279005 | Cirrhosis and chronic liver disease |
| 197284004 | Chronic active hepatitis |
| 197286002 | Recurrent hepatitis |
| 197291001 | Unilobular portal cirrhosis |
| 197293003 | Diffuse nodular cirrhosis |
| 197294009 | Fatty portal cirrhosis |
| 197296006 | Capsular portal cirrhosis |
| 197299004 | Pigmentary portal cirrhosis |
| 197300007 | Pipestem portal cirrhosis |
| 197301006 | Toxic portal cirrhosis |
| 197303009 | Bacterial portal cirrhosis |
| 197305002 | Syphilitic portal cirrhosis |
| 197310003 | Biliary cirrhosis of children |
| 197316009 | Portal fibrosis without cirrhosis |
| 197321007 | Steatosis of liver |
| 197324004 | Liver abscess and sequelae of chronic liver disease |
| 197347003 | Hepatitis in late syphilis |
| 197348008 | Hepatitis in secondary syphilis |
| 197355005 | Toxic liver disease with cholestasis |
| 197356006 | Toxic liver disease with hepatic necrosis |
| 197359004 | Toxic liver disease with chronic persistent hepatitis |
| 197360009 | Toxic liver disease with chronic lobular hepatitis |
| 197361008 | Toxic liver disease with chronic active hepatitis |
| 197362001 | Toxic liver disease with fibrosis and cirrhosis of liver |
| 197367007 | Hepatic granulomas in berylliosis |
| 197368002 | Hepatic granulomas in sarcoidosis |
| 197441003 | Primary sclerosing cholangitis |
| 197442005 | Secondary sclerosing cholangitis |
| 19943007 | Cirrhosis of liver |
| 204781002 | Congenital absence of hepatic ducts |
| 204782009 | Atresia of hepatic ducts |
| 204787003 | Congenital absence of liver and/or gallbladder |
| 213153001 | Liver transplant failure and rejection |
| 213230009 | Hepatic failure as a complication of care |
| 213231008 | Hepatorenal syndrome as a complication of care |
| 21861000 | Micronodular cirrhosis |
| 22508003 | Hepatic failure due to a procedure |
| 22846003 | Hepatorenal syndrome following delivery |
| 234689009 | Relapsing pancreatitis |
| 235458006 | Exploration of liver transplant |
| 235494005 | Chronic pancreatitis |
| 235865005 | Hepatitis D superinfection of hepatitis B carrier |
| 235869004 | Chronic viral hepatitis B with hepatitis D |
| 235870003 | Chronic non-A non-B hepatitis |
| 235875008 | Alcoholic hepatitis |
| 235877000 | Ischemic hepatitis |
| 235880004 | Alcoholic fibrosis and sclerosis of liver |
| 235881000 | Alcoholic hepatic failure |
| 235884008 | Fulminant hepatic failure |
| 235885009 | Subfulminant hepatic failure |
| 235886005 | Chronic hepatic failure |
| 235889003 | Drug-induced chronic hepatitis |
| 235890007 | Autoimmune liver disease |
| 235895002 | Laennec's cirrhosis, non-alcoholic |
| 235896001 | Infectious cirrhosis |
| 235897005 | Hypoxia-associated cirrhosis |
| 235898000 | Pericellular fibrosis of congenital syphilis |
| 235899008 | Hepatic sclerosis |
| 235900003 | Portal and splenic vein sclerosis |
| 235901004 | Hepatic fibrosis with hepatic sclerosis |
| 235902006 | Intrahepatic phlebosclerosis and fibrosis |
| 235903001 | Metabolic and genetic disorder affecting the liver |
| 235908005 | Glycogen storage disease type IX |
| 235909002 | Antichymotrypsin deficiency-alpha-1 |
| 235910007 | Liver transplant disorder |
| 235911006 | Liver transplant rejection |
| 235912004 | Liver transplant failure |
| 235915002 | Synthetic defect of bile acids |
| 235916001 | Ichthyosis congenita with biliary atresia |
| 235917005 | Sclerosing cholangitis |
| 235951009 | Gallstone chronic pancreatitis |
| 235952002 | Alcohol-induced chronic pancreatitis |
| 235953007 | Idiopathic chronic pancreatitis |
| 235954001 | Obstructive chronic pancreatitis |
| 235955000 | Drug-induced chronic pancreatitis |
| 235956004 | Familial chronic pancreatitis |
| 237964009 | Glycogen synthase deficiency |
| 237965005 | Phosphate transport defect |
| 237966006 | Glucose transport defect |
| 238033007 | 3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency |
| 238035000 | Delta-4-3-oxosteroid-5-beta-reductase deficiency |
| 240792005 | Symmer's pipe-stem fibrosis |
| 253807009 | Intrahepatic biliary atresia |
| 253808004 | Congenital kink of cystic duct |
| 26206000 | Hepatic coma due to viral hepatitis B |
| 266468003 | Cirrhosis - non-alcoholic |
| 266469006 | Multilobular portal cirrhosis |
| 266470007 | Cardiac portal cirrhosis |
| 266471006 | Juvenile portal cirrhosis |
| 267424007 | Generalized glycogenosis |
| 271440004 | Cirrhosis secondary to cholestasis |
| 27156006 | Posthepatitic cirrhosis |
| 27280000 | Liver transplant with recipient hepatectomy |
| 274864009 | Glycogen storage disease, type II |
| 276668008 | Congenital non-A non-B hepatitis infection |
| 276723008 | Intrahepatic biliary hypoplasia |
| 278929008 | Congenital hepatitis C infection |
| 28009009 | Liver transplant without recipient hepatectomy |
| 281095009 | Congenital stricture of common bile duct |
| 281388009 | Human immunodeficiency virus-related sclerosing cholangitis |
| 29291001 | Glycogen storage disease, type VI |
| 29633007 | Glycogen storage disease |
| 297251003 | Glycogen phosphorylase kinase deficiency, X-linked |
| 297252005 | Glycogen phosphorylase kinase deficiency, autosomal recessive |
| 297253000 | Cardiac glycogen phosphorylase kinase deficiency |
| 297254006 | Hepatic and muscle glycogen phosphorylase kinase deficiency |
| 297255007 | Hepatic glycogen phosphorylase kinase deficiency |
| 301009006 | Calcific chronic pancreatitis |
| 30102006 | Glucose-6-phosphate transport defect |
| 30188007 | Alpha-1-antitrypsin deficiency |
| 307757001 | Chronic alcoholic hepatitis |
| 308129003 | Esophageal varices in cirrhosis of the liver |
| 309783001 | Esophageal varices in alcoholic cirrhosis of the liver |
| 31005002 | Hepatorenal syndrome due to a procedure |
| 314963000 | Local recurrence of malignant tumor of liver |
| 31712002 | Primary biliary cholangitis |
| 31742004 | Arteriohepatic dysplasia |
| 328383001 | Chronic liver disease |
| 33144001 | Parasitic cirrhosis |
| 33167004 | Complication of transplanted liver |
| 34736002 | Chronic passive congestion of liver |
| 34742003 | Portal hypertension |
| 347891000119103 | Chronic hepatitis C with stage 3 fibrosis |
| 3650004 | Congenital absence of liver |
| 367406009 | Deficiency of alpha-dextrin endo-1,6-alpha-glucosidase |
| 36760000 | Hepatosplenomegaly |
| 370492003 | Copper storage associated hepatitis |
| 371139006 | Early cirrhosis |
| 37666005 | Glycogen storage disease type X |
| 37688005 | Clonorchiasis with biliary cirrhosis |
| 38662009 | Chronic persistent type B viral hepatitis |
| 397575003 | Viral hepatitis, type G |
| 406584008 | Non-A, non-B, non-C hepatitis |
| 407000 | Congenital hepatomegaly |
| 408335007 | Autoimmune hepatitis |
| 40946000 | Hepatic coma due to viral hepatitis |
| 41309000 | Alcoholic liver damage |
| 41527003 | Glycogen storage disease type VIII |
| 41889008 | Chronic persistent hepatitis |
| 419097006 | Danon disease |
| 419728003 | Portal cirrhosis |
| 420054005 | Alcoholic cirrhosis |
| 424099008 | Hepatic coma due to acute hepatitis B |
| 424340000 | Hepatic coma due to chronic hepatitis B |
| 425413006 | Drug-induced cirrhosis of liver |
| 426356008 | Orthotopic transplantation of whole liver |
| 427022004 | Liver disease due to cystic fibrosis |
| 427044009 | Fulminant hepatitis |
| 428198008 | Transplantation of hepatocytes |
| 431222008 | Acute rejection of liver transplant |
| 432772009 | Hyperacute rejection of liver transplant |
| 432777003 | Accelerated rejection of liver transplant |
| 432908002 | Chronic rejection of liver transplant |
| 43904005 | Macronodular cirrhosis |
| 44047000 | Zieve's syndrome |
| 442134007 | Hepatitis B associated with Human immunodeficiency virus infection |
| 442191002 | Steatohepatitis |
| 442374005 | Hepatitis B and hepatitis C |
| 442685003 | Nonalcoholic steatohepatitis |
| 444707001 | Glycogen storage disease type Ia |
| 444918006 | Sequela of chronic liver disease |
| 446698005 | Reactivation of hepatitis B viral hepatitis |
| 450880008 | Chronic hepatitis E |
| 45256007 | Cruveilhier-Baumgarten syndrome |
| 459062008 | Fatal congenital nonlysosomal heart glycogenosis |
| 50167007 | Chronic active type B viral hepatitis |
| 50325005 | Alcoholic fatty liver |
| 50711007 | Viral hepatitis type C |
| 51038004 | Congenital obstruction of bile duct |
| 51292008 | Hepatorenal syndrome |
| 53425008 | Anicteric type B viral hepatitis |
| 536002 | Glissonian cirrhosis |
| 55912009 | Glycogen storage disease, type V |
| 5667009 | Hunter's syndrome, mild form |
| 57339008 | Chronic lobular hepatitis |
| 58282009 | Relapsing viral hepatitis |
| 59927004 | Hepatic failure |
| 60037002 | Chronic persistent viral hepatitis |
| 60498001 | Congenital viral hepatitis B infection |
| 6075009 | Glycogen storage disease, hepatic form |
| 61598006 | Glycogenosis with glucoaminophosphaturia |
| 6183001 | Indian childhood cirrhosis |
| 61977001 | Chronic type B viral hepatitis |
| 62216007 | Familial arthrogryposis-cholestatic hepatorenal syndrome |
| 62484002 | Hepatic fibrosis |
| 63246000 | Cholestanol storage disease |
| 66071002 | Viral hepatitis type B |
| 66870002 | Chronic active viral hepatitis |
| 66937008 | Glycogen storage disease, type III |
| 68094008 | Congenital hypoplasia of bile duct |
| 698305006 | Awaiting transplantation of liver |
| 699189004 | North American Indian childhood cirrhosis |
| 700463002 | Alpha-methylacyl-CoA racemase deficiency disorder |
| 702777009 | Liver transplant recipient |
| 702969000 | Reactivation of hepatitis C viral hepatitis |
| 703866000 | Chronic hepatitis C with stage 2 fibrosis |
| 704201006 | Liver transplant planned |
| 707341005 | Viral hepatitis type D |
| 70737009 | Mucopolysaccharidosis type II |
| 707420003 | Portal hypertension due to cystic fibrosis |
| 707551007 | Pulmonary interstitial glycogenosis |
| 708198006 | Chronic active hepatitis C |
| 708248004 | End stage liver disease |
| 7111000119109 | Viral hepatitis type E |
| 713181003 | Chronic alcoholic liver disease |
| 713370005 | Acute on chronic alcoholic liver disease |
| 713529007 | Steatosis of liver caused by retroviral protease inhibitor |
| 713542007 | Portal hypertension caused by antiretroviral drug |
| 713965007 | Sclerosis of portal vein and splenic vein caused by antiretroviral drug |
| 713966008 | Occult chronic type B viral hepatitis |
| 715401008 | Primary biliary cirrhosis co-occurrent with systemic scleroderma |
| 715864007 | Non-Wilsonian hepatic copper toxicosis of infancy and childhood |
| 716203000 | Decompensated cirrhosis of liver |
| 717047007 | Bile acid coenzyme A ligase deficiency and defective amidation |
| 717156002 | Biliary atresia with splenic malformation syndrome |
| 717187000 | Nephronophthisis hepatic fibrosis syndrome |
| 717821004 | Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency |
| 719452004 | Congenital bronchobiliary fistula |
| 719454003 | Congenital bile acid synthesis defect type 3 |
| 720394008 | Congenital tracheobiliary fistula |
| 721099001 | Adult polyglucosan body disease |
| 721710005 | Fibrosis of liver caused by alcohol |
| 721711009 | Autoimmune hepatitis type 1 |
| 721712002 | Autoimmune hepatitis type 2 |
| 721713007 | Autoimmune hepatitis type 3 |
| 721847002 | Joubert syndrome with congenital hepatic fibrosis |
| 722302009 | Glycogen storage disease type II infantile onset |
| 722343009 | Glycogen storage disease type II late onset |
| 722867009 | Idiopathic portal hypertension |
| 722870008 | Immunoglobulin G4-related sclerosing cholangitis |
| 722871007 | Groove pancreatitis |
| 723360007 | Familial hypercholanemia |
| 723583009 | Steroid dehydrogenase deficiency and dental anomaly syndrome |
| 723829000 | Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome |
| 724278007 | Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome |
| 724540009 | Tropical calcific chronic pancreatitis |
| 724766009 | Chorea co-occurrent and due to Wilson disease |
| 725026008 | Hepatic glycogen synthase deficiency |
| 725027004 | Muscle and heart glycogen synthase deficiency |
| 725416005 | Cardiomyopathy due to cirrhosis of liver |
| 725938001 | Cirrhosis of liver caused by methotrexate |
| 725939009 | Cirrhosis of liver caused by amiodarone |
| 725940006 | Cirrhosis of liver caused by methyldopa |
| 7265005 | Glycogen storage disease, type I |
| 72925005 | Congenital cystic disease of liver |
| 73146005 | Hunter's syndrome, severe form |
| 735451005 | Chronic infection caused by Hepatitis D virus |
| 735733008 | Cirrhosis of liver co-occurrent and due to primary sclerosing cholangitis |
| 737202006 | Fibropolycystic disease of liver |
| 737297006 | Transplanted liver present |
| 74162007 | Progressive intrahepatic cholestasis |
| 74669004 | Cardiac cirrhosis |
| 74973004 | Chronic fibrosing pancreatitis |
| 76301009 | Florid cirrhosis |
| 764962002 | Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 |
| 767291004 | Chronic pancreatitis due to acute alcohol intoxication |
| 767809001 | Chronic hepatitis C caused by hepatitis C virus genotype 6 |
| 767810006 | Chronic hepatitis C caused by hepatitis C virus genotype 5 |
| 76783007 | Chronic hepatitis |
| 768006009 | Chronic hepatitis C caused by Hepatitis C virus genotype 3 |
| 768125005 | Chronic hepatitis C caused by Hepatitis C virus genotype 2 |
| 768126006 | Chronic hepatitis C caused by Hepatitis C virus genotype 4 |
| 768127002 | Chronic hepatitis C caused by Hepatitis C virus genotype 1 |
| 768288001 | Chronic hepatitis C caused by Hepatitis C virus genotype 1b |
| 768289009 | Chronic hepatitis C caused by Hepatitis C virus genotype 1a |
| 771149000 | Hepatic fibrosis, renal cyst, intellectual disability syndrome |
| 773415005 | Contiguous ABCD1 DXS1357E deletion syndrome |
| 773584001 | Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome |
| 773737004 | Nephrocystin 3-related Meckel-like syndrome |
| 774148007 | Polyglucosan body myopathy type 1 |
| 774151000 | Ferro-cerebro-cutaneous syndrome |
| 774204006 | Growth retardation, mild developmental delay, chronic hepatitis syndrome |
| 77480004 | Congenital biliary atresia |
| 776981000000103 | Cirrhosis associated with cystic fibrosis |
| 78208005 | Pigment cirrhosis |
| 782771007 | Mitochondrial deoxyribonucleic acid depletion syndrome hepatocerebrorenal form |
| 783734000 | Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency |
| 784346006 | Navajo neurohepatopathy |
| 79607001 | Congenital hepatic fibrosis |
| 79720007 | Chronic nonalcoholic liver disease |
| 80378000 | Neonatal hepatosplenomegaly |
| 80770009 | Secondary syphilis of liver |
| 819953000 | Glycogen storage disease due to muscle phosphorylase kinase deficiency |
| 824841000000105 | Hepatitis C genotype 1 |
| 824851000000108 | Hepatitis C genotype 2 |
| 824871000000104 | Hepatitis C genotype 3 |
| 824881000000102 | Hepatitis C genotype 4 |
| 824891000000100 | Hepatitis C genotype 5 |
| 824901000000104 | Hepatitis C genotype 6 |
| 82821008 | Congenital atresia of extrahepatic bile duct |
| 831000119103 | Cirrhosis of liver due to chronic hepatitis C |
| 838375006 | Chronic infectious pancreatitis |
| 838377003 | Chronic hepatitis C co-occurrent with human immunodeficiency virus infection |
| 838380002 | Chronic hepatitis B co-occurrent with hepatitis C and hepatitis D |
| 853761000000103 | Living donor liver transplantation |
| 86028001 | Syphilis of liver |
| 860858001 | Glycogen storage disease due to muscle pyruvate kinase deficiency |
| 860860004 | Glycogen storage disease type IXB |
| 863957008 | Chronic necrosis of liver |
| 86454000 | Postnecrotic cirrhosis |
| 870517000 | Periportal fibrosis |
| 871619002 | Cirrhosis of liver due to and following cardiac procedure |
| 88518009 | Wilson's disease |
| 890201000 | Congenital absence of cystic duct |
| 89580002 | Cryptogenic cirrhosis |
| 89597008 | Glycogen storage disease, type VII |
| 89789003 | Chronic aggressive viral hepatitis |
| 96601000119101 | Aftercare for liver transplant done |
| 9843006 | Chronic lymphocytic cholangitis-cholangiohepatitis |
Codes not in the full codelist are in faint grey.