| Eponyms in category: Liver |
| 82
main and alternative
entries found.
|
|
| Addison-Gull syndrome (Rayer's disease) |
| A disorder characterized by vitiligoides of the skin, chronic jaundice, splenomegaly, and hepatomegaly.
|
| Aguecheek's disease |
|
| Baber's syndrome |
| A syndrome of cirrhosis of the liver with clinical features similar to those found in the Fanconi syndrome. |
| Ballard's syndrome |
| A syndrome of unknown aetiology marked by hepatomegaly, splenomegaly, and pathologic fractures. |
| Baumgarten’s portal hypertension variant syndrome (Cruveilhier-Baumgarten disease) |
| Cirrhosis of the liver without ascites. |
| Baumgarten’s syndrome (Cruveilhier-Baumgarten disease) |
| Cirrhosis of the liver without ascites. |
| Bean's dollar bill skin (Bean's syndrome) |
| A syndrome of skin changes on the upper trunk typical of chronic liver disease. |
| Bean's syndrome |
| A syndrome of skin changes on the upper trunk typical of chronic liver disease. |
| Bearn-Kunkel-Slater syndrome |
| Obsolete term for "lupoide hepatitis" as course of an autoimmune chronic hepatitis seen in young women. |
| Bearn-Künkel syndrome (Bearn-Kunkel-Slater syndrome) |
| Obsolete term for "lupoide hepatitis" as course of an autoimmune chronic hepatitis seen in young women. |
| Bergmann's bilirubin tolerance test (Bergmann-Eilbott test) |
| Bilirubin excretion test of liver function. |
| Bergmann-Eilbott bilirubin tolerance test (Bergmann-Eilbott test) |
| Bilirubin excretion test of liver function. |
| Bergmann-Eilbott test |
| Bilirubin excretion test of liver function. |
| Bongiovanni-Eisenmenger syndrome (William J. Eisenmenger) |
| A chronic liver illness of unknown aetiology. |
| Budd's cirrhosis |
| Chronic hepatomegaly believed to be caused by intestinal intoxication. |
| Budd's disease (Budd-Chiari syndrome) |
| A rare disorder marked by cirrhosis of the liver and ascites due to an obstruction of the hepatic vein by a blood clot or tumor. |
| Budd's jaundice (Budd-Chiari syndrome) |
| A rare disorder marked by cirrhosis of the liver and ascites due to an obstruction of the hepatic vein by a blood clot or tumor. |
| Budd-Chiari syndrome |
| A rare disorder marked by cirrhosis of the liver and ascites due to an obstruction of the hepatic vein by a blood clot or tumor. |
| Chiari’s disease (Budd-Chiari syndrome) |
| A rare disorder marked by cirrhosis of the liver and ascites due to an obstruction of the hepatic vein by a blood clot or tumor. |
| Chiari’s syndrome (Budd-Chiari syndrome) |
| A rare disorder marked by cirrhosis of the liver and ascites due to an obstruction of the hepatic vein by a blood clot or tumor. |
| Cirrhose alcoolo-tuberculeuse de Hutinel et Sabourin (French) (Hutinel and Sabourin's alcoholic-tuberculous cirrhosis) |
| Hypertrophic fatty cirrhosis the liver of alcoholic or tuberculous origin. |
| Cruveilhier-Baumgarten cirrhosis (Cruveilhier-Baumgarten disease) |
| Cirrhosis of the liver without ascites. |
| Cruveilhier-Baumgarten disease |
| Cirrhosis of the liver without ascites. |
| Cruveilhier-Baumgarten sound (Cruveilhier-Baumgarten disease) |
| Cirrhosis of the liver without ascites. |
| Cruveilhier-Baumgarten syndrome (Cruveilhier-Baumgarten disease) |
| Cirrhosis of the liver without ascites. |
| Flint's syndrome (Austin Flint, Sr.) (Heyd's syndrome) |
| The development of renal dysfunction in patients with severe liver disease (acute or chronic) in the absence of any other identifiable causes of renal pathology. |
| Frerichs' symptom |
| The presence of leucine and tyrosine in urinary sediment in acute yellow atrophy of the liver. |
| Frerichs' syndrome (Heyd's syndrome) |
| The development of renal dysfunction in patients with severe liver disease (acute or chronic) in the absence of any other identifiable causes of renal pathology. |
| Gilbert's disease (Gilbert's syndrome) |
| A hereditary, congenital, benign, chronic, intermittent hyperbilirubinemia. |
| Gilbert's sign |
| Patient's with liver cirrhosis pass more urine when fasting than after a meal.
|
| Gilbert's syndrome |
| A hereditary, congenital, benign, chronic, intermittent hyperbilirubinemia. |
| Gilbert-Lereboullet syndrome (Gilbert's syndrome) |
| A hereditary, congenital, benign, chronic, intermittent hyperbilirubinemia. |
| Gilbert-Meulengracht syndrome (Gilbert's syndrome) |
| A hereditary, congenital, benign, chronic, intermittent hyperbilirubinemia. |
| Glisson's triad (Glisson's triangle) |
| The periportal tracts of the liver.
|
| Glisson's triangle |
| The periportal tracts of the liver.
|
| Glissonian cirrhosis |
| Chronic inflammation of the peritoneal coat of the liver with thickening and subsequent contraction, resulting in atrophy and deformity of the liver. |
| Glissonitis |
| Inflammation of Glisson’s capsule.
|
| Hanot's cirrhosis |
| Fibrosis of the liver due to obstruction or infection of the major extra- or intrahepatic bile ducts. |
| Hanot's syndrome (Hanot's cirrhosis) |
| Fibrosis of the liver due to obstruction or infection of the major extra- or intrahepatic bile ducts. |
| Hanot-Kiener disease (Hanot-Kiener syndrome) |
| Historic term for a diffuse chronic mesenchymatous hepatitis. |
| Hanot-Kiener syndrome |
| Historic term for a diffuse chronic mesenchymatous hepatitis. |
| Hanot-MacMahon-Thannhauser syndrome |
| Historical, no longer used term for a so-called xanthomatous biliary cirrhosis. |
| Hansen-Larsen-Berg syndrome |
| A familial syndrome of progressive cone dystrophy with total colour blindness, optic disc pallor, thin retinal blood vessels, and retinal dystrophy. |
| Heyd's syndrome |
| The development of renal dysfunction in patients with severe liver disease (acute or chronic) in the absence of any other identifiable causes of renal pathology. |
| Hutinel and Sabourin's alcoholic-tuberculous cirrhosis |
| Hypertrophic fatty cirrhosis the liver of alcoholic or tuberculous origin. |
| Hutinel's cirrhosis |
| Cirrhosis of the liver associated with tuberculous pericarditis in children. |
| Hutinel's syndrome (Hutinel's cirrhosis) |
| Cirrhosis of the liver associated with tuberculous pericarditis in children. |
| Hypertrophic cirrhosis of Hanot (Hanot's cirrhosis) |
| Fibrosis of the liver due to obstruction or infection of the major extra- or intrahepatic bile ducts. |
| Kiener’s disease (Hanot-Kiener syndrome) |
| Historic term for a diffuse chronic mesenchymatous hepatitis. |
| Kinnier Wilson's disease (Wilson's disease) |
| A chronic disease of brain and liver with progressive neurological dysfunction, due to a disturbance of copper metabolism. |
| Künkel's syndrome (Bearn-Kunkel-Slater syndrome) |
| Obsolete term for "lupoide hepatitis" as course of an autoimmune chronic hepatitis seen in young women. |
| Laënnec's cirrhosis |
| Cirrhosis of the liver - without jaundice - seen in chronic alcoholism and malnutrition. |
| Laënnec’s syndrome (Laënnec's cirrhosis) |
| Cirrhosis of the liver - without jaundice - seen in chronic alcoholism and malnutrition. |
| MacMahon-Tannhauser syndrome (Hanot-MacMahon-Thannhauser syndrome) |
| Historical, no longer used term for a so-called xanthomatous biliary cirrhosis. |
| Marchand's syndrome |
| A cirrhosis clinically identical to liver cirrhosis but with a different pathologic pattern. |
| Meulengracht's icterus (Gilbert's syndrome) |
| A hereditary, congenital, benign, chronic, intermittent hyperbilirubinemia. |
| Meulengracht's syndrome (Gilbert's syndrome) |
| A hereditary, congenital, benign, chronic, intermittent hyperbilirubinemia. |
| Meulengracht’s disease (Gilbert's syndrome) |
| A hereditary, congenital, benign, chronic, intermittent hyperbilirubinemia. |
| Meyenburg's complex (Von Meyenburg's complex) |
| Andenoma-like hamartomas in the liver. |
| Morgagni-Laënnec syndrome/cirrhosis (Laënnec's cirrhosis) |
| Cirrhosis of the liver - without jaundice - seen in chronic alcoholism and malnutrition. |
| Mosse's polycythaemia (Mosse's syndrome) |
| Liver cirrhosis, liver cirrhosis-polycythaemia, polycythaemia-hepatocirrhosis syndrome. |
| Mosse's syndrome |
| Liver cirrhosis, liver cirrhosis-polycythaemia, polycythaemia-hepatocirrhosis syndrome. |
| Mosse-Marchand-Mallory cirrhosis |
| A usually fatal form of cirrhosis of the liver.
|
| Pégot-Cruveilhier-Baumgarten syndrome (Cruveilhier-Baumgarten disease) |
| Cirrhosis of the liver without ascites. |
| Rayer's disease |
| A disorder characterized by vitiligoides of the skin, chronic jaundice, splenomegaly, and hepatomegaly.
|
| Reynolds' syndrome (Telfer B. Reynolds) |
| A syndrome of chronic liver disease characterized by the coexistence of progressive systemic sclerosis and primary biliary cirrhosis. |
| Rokitansky’s disease (Budd-Chiari syndrome) |
| A rare disorder marked by cirrhosis of the liver and ascites due to an obstruction of the hepatic vein by a blood clot or tumor. |
| Rotor's syndrome |
| A rare idiopathic form of hyperbilirubinaemia. |
| Rotor, Manahan and Florentin syndrome (Rotor's syndrome) |
| A rare idiopathic form of hyperbilirubinaemia. |
| Rotor’s type of bilirubinaemia (Rotor's syndrome) |
| A rare idiopathic form of hyperbilirubinaemia. |
| Schiff's biliary cycle |
| The return to the liver of bile salts from the intestine.
|
| Syndrome d'Hutinel (French) (Hutinel's cirrhosis) |
| Cirrhosis of the liver associated with tuberculous pericarditis in children. |
| Tannhauser-Magendantz syndrome (Hanot-MacMahon-Thannhauser syndrome) |
| Historical, no longer used term for a so-called xanthomatous biliary cirrhosis. |
| von Bergmann's test (Bergmann-Eilbott test) |
| Bilirubin excretion test of liver function. |
| Von Meyenburg's complex |
| Andenoma-like hamartomas in the liver. |
| von Rokitansky disease (Budd-Chiari syndrome) |
| A rare disorder marked by cirrhosis of the liver and ascites due to an obstruction of the hepatic vein by a blood clot or tumor. |
| Westphal's pseudosclerosis (Wilson's disease) |
| A chronic disease of brain and liver with progressive neurological dysfunction, due to a disturbance of copper metabolism. |
| Westphal-Strümpell disease (Wilson's disease) |
| A chronic disease of brain and liver with progressive neurological dysfunction, due to a disturbance of copper metabolism. |
| Westphal-Strümpell pseudosclerosis (Wilson's disease) |
| A chronic disease of brain and liver with progressive neurological dysfunction, due to a disturbance of copper metabolism. |
| Westphal-Strümpell syndrome (Wilson's disease) |
| A chronic disease of brain and liver with progressive neurological dysfunction, due to a disturbance of copper metabolism. |
| Wilson's disease |
| A chronic disease of brain and liver with progressive neurological dysfunction, due to a disturbance of copper metabolism. |
| Wilson-Konovalov disease (Wilson's disease) |
| A chronic disease of brain and liver with progressive neurological dysfunction, due to a disturbance of copper metabolism. |
|
