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Dubin-johnson Syndrome
Dubin-Johnson syndrome
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Hepatology
(181)
Alpha 1 antitrypsin deficiency
Bile acid
Cholelithiasis
Cholestasis
Common bile duct
Common bile duct
Crigler-najjar syndrome
Direct bilirubin
Gilbert syndrome
Hepatobiliary
Hyperbilirubinemia
Intrahepatic Cholestasis of Pregnancy
Ischemic hepatitis
Liver biopsy
Lucey-Driscoll syndrome
Neonatal jaundice
Portal hypertension
Primary biliary cirrhosis
Rotor syndrome
Urobilinogen
ATC code A05
Acanthocyte
Accessory bile duct
Aceruloplasminemia
Acute liver failure
Alagille syndrome
Alanine transaminase
Alcoholic liver disease
Alpha-Amanitin
Amanin
Amaninamide
Amanullin
Amanullinic acid
Artificial extracorporeal liver support
Ascending cholangitis
Banti's syndrome
Ben Hardwick
Bile
Bile acid sequestrant
Bile acids
Bile canaliculus
Bile duct
Biliary atresia
Biliary fistula
Bilirubin (data page)
Bioartificial liver device
Budd-Chiari syndrome
CIOMS/RUCAM scale
Canals of Hering
Carnitine palmitoylt- ransferase I deficiency
Carnitine palmitoylt- ransferase II deficiency
Caroli disease
Ceruloplasmin
Child-Pugh score
Cholangiocarcinoma
Cholangiography
Cholecystitis
Cholecystokinin
Choledocholithiasis
Cholesteryl ester storage disease
Cholestyramine
Cirrhosis
Clonorchiasis
Colesevelam
Common hepatic duct
Congestive hepatopathy
Councilman body
Cruveilhie- r-Baumgarten bruit
Cruveilhie- r-Baumgarten disease
Cystic duct
Cystohepatic triangle
Deaths from liver disease
Delcath Systems, Inc.
Desmoplastic small round cell tumor
Discriminant function
Drug metabolism
Ductopenia
Echinococcus
Elevated transaminases
Enterohepatic circulation
Falciform ligament
Fatty acid metabolism
Fatty liver
Fetor hepaticus
FibroTest
Fibrolamellar hepatocellular carcinoma
Focal fatty liver
Focal nodular hyperplasia
Gallbladder
Gallbladder polyp
Gamma-Amanitin
Gaucher's disease
Glucagon
Gluconeogenesis
Glucuronic acid
Glycogen
Glycogen storage disease
Glycogen storage disease type 0
Glycogen storage disease type I
Glycogen storage disease type II
Glycogen storage disease type III
Glycogen storage disease type IV
Glycogenolysis
HFE hereditary hemochromatosis
Haemobilia
Hepatectomy
Hepatic encephalopathy
Hepatic veno-occlusive disease
Hepatitis
Hepato-biliary diseases
Hepatoblastoma
Hepatocellular adenoma
Hepatocellular carcinoma
Hepatolithiasis
Hepatologists
Hepatomegaly
Hepatoprotection
Hepatopulmonary syndrome
Hepatorenal ligament
Hepatorenal syndrome
Hepatosplenomegaly
Hepatotoxicity
Hepatotoxin
Hepcidin
Hurler syndrome
Infantile hemangioen- dothelioma
Interlobular bile ducts
International Hepato-Pan- creato-Bilary Association
Intrahepatic bile ducts
Klatskin tumor
Laennec's cirrhosis
Lipid therapy
Lipolysis
Liver cancer
Liver dialysis
Liver disease
Liver failure
Liver fluke
Liver function tests
Liver resection
Liver transplantation
Liver tumor
Lábrea fever
Meckel syndrome
Metastatic liver disease
Model for End-Stage Liver Disease
Murphy's sign
Nature Clinical Practice Gastroenterology and Hepatology
Neonatal hemochromatosis
Omegaven
Omenn syndrome
Oral cholecystography
Pediatric end-stage liver disease
Percutaneous hepatic perfusion
Perisinusoidal
Portal vein thrombosis
Portopulmonary hypertension
Portosystemic shunt
Primary carnitine deficiency
Primary sclerosing cholangitis
Pringle manoeuvre
Proamanullin
Progressive familial intrahepatic cholestasis
Revesz syndrome
Reye's syndrome
Reynolds syndrome
Round ligament of liver
Schistosomiasis
Secondary sclerosing cholangitis
Serum-ascites albumin gradient
Transaminase
Transcatheter arterial chemoembolization
Transjugular intrahepatic portosystemic shunt
Wilson's disease
Xanthelasma
Xanthoma
Yellow fever
Zahn Infarct
Zellweger syndrome
Zieve's syndrome
beta-Amanitin
epsilon-Amanitin
more...
Autosomal recessive disorders
Gunther disease
Carbamoyl phosphate synthetase I deficiency
Leukodystrophy, globoid cell
Cerebrotendineous xanthomatosis
Dubowitz syndrome
Rotor syndrome
Lucey-Driscoll syndrome
Gastroenterology
(9)
Autoimmune hepatitis
Choledochal cyst
Hyperbilirubinemia
Cholestasis
Gilbert syndrome
Gilbert syndrome
Alpha 1 antitrypsin deficiency
Primary biliary cirrhosis
Cholelithiasis
Portal hypertension
more...
Syndromes
(10)
Hereditary sensory and autonomic neuropathies
Fetofetal transfusion
Distal Arthrogryposis, Type IIA
5p- syndrome
4p- syndrome
4p- syndrome
Rotor syndrome
Crigler-najjar syndrome
Lucey-Driscoll syndrome
Gilbert syndrome
Dubowitz syndrome
more...
Genetic disorders
(23)
ALAD porphyria
Hyperostosis, cortical, congenital
Adrenoleuk- odystrophy
Acute intermittent porphyria
Galactosemias
Galactosemias
Variegate porphyria
Hereditary coproporphyria
Dyskeratosis congenita
Duchenne muscular dystrophy
Muscular dystrophy
Rotor syndrome
Crigler-najjar syndrome
Lucey-Driscoll syndrome
Gilbert syndrome
Gunther disease
Carbamoyl phosphate synthetase I deficiency
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Cerebrotendineous xanthomatosis
5p- syndrome
Alpha 1 antitrypsin deficiency
4p- syndrome
Dubowitz syndrome
more...
Digestive system
Duodenal
Biliary tract
Ampulla of vater
Hyperbilirubinemia
Common bile duct
Hepatobiliary
Tetrapyrroles
(38)
Coproporphyrin
Heme
Bilin (biochemistry)
Bilirubin (data page)
Biliverdin
Biliverdin
Chlorophyll
Chlorophyll a
Chlorophyll b
Chlorophyll c1
Chlorophyll c2
Chlorophyll d
Chlorophyllin
Coproporphyrinogen III
Corrin
Corrole
Direct bilirubin
Heme C
Heme a
Heme b
Heme o
Hydroxymethylbilane
Phycobilin
Phycocyanobilin
Phycoerythrobilin
Phycoerythrocyanin
Phycourobilin
Porphin
Protoporphyrin
Protoporphyrin IX
Talaporfin
Temoporfin
Tetraphenylporphine sulfonate
Tetrapheny- lporphyrin
Tetrapyrrole
Urobilin
Urobilinogen
Uroporphyrinogen III
Zinc protoporphyrin
more...
Porphyrias
(10)
Porphyria, hepatic
ALAD porphyria
Acute intermittent porphyria
Erythropoietic porphyria
Erythropoietic protoporphyria
Erythropoietic protoporphyria
Hepatoeryt- hropoietic porphyria
Hereditary coproporphyria
Porphyria
Porphyria cutanea tarda
Variegate porphyria
more...
Haemorrhagic and haematological disorders of fetus and newborn
Kernicterus
Haemorrhagic disease of the newborn
Neonatal jaundice
Polycythemia
Diseases and disorders
(58)
Disintegrative psychosis
Chronic idiopathic jaundice
Hereditary hyperbilirubinemia
Icterus
Glossopharyngeal nerve diseases
Glossopharyngeal nerve diseases
Type i complex regional pain syndrome
Myopathies, structural, congenital
Enterocolitis, pseudomembranous
Physiologic nystagmus
Histiocytosis non-langerhans-cell
Postpoliomyelitis syndrome
Olfaction disorders
Intervertebral disk displacement
Rosenthal syndrome
Diencephalic syndrome
Optic neuropathy, ischemic
Dermatitis exfoliativa
Diffuse parenchymal lung disease
Dwarfism
Otosclerosis
Hyperbilirubinemia
Rotor syndrome
Cholestasis
Lucey-Driscoll syndrome
Gilbert syndrome
Gunther disease
Hyperostosis, cortical, congenital
Carbamoyl phosphate synthetase I deficiency
Purpura, schoenlein-henoch
Acute intermittent porphyria
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Fetofetal transfusion
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Encephalitis, arbovirus
Hepatitis e
Autoimmune hepatitis
Cerebrotendineous xanthomatosis
Distal Arthrogryposis, Type IIA
Galactosemias
Brachial plexus neuropathies
Hepatoeryt- hropoietic porphyria
5p- syndrome
Alpha 1 antitrypsin deficiency
Primary biliary cirrhosis
Cholelithiasis
Variegate porphyria
Hereditary coproporphyria
Choledochal cyst
Portal hypertension
Dyskeratosis congenita
Neonatal jaundice
Hepatitis d
Duchenne muscular dystrophy
Dubowitz syndrome
Kernicterus
Muscular dystrophy
more...
See also
(20)
Diseases and disorders
Physiologic
CMOAT
Heme metabolism intermediates
Purpura, schoenlein-henoch
Purpura, schoenlein-henoch
Hemolysis
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Encephalitis, arbovirus
Hepatitis e
ATP binding cassette
De Toni-Fanconi Syndrome
Multidrug resistance
Cyproterone acetate
Brachial plexus neuropathies
Hepatoeryt- hropoietic porphyria
Abdominal pain
Names
Places
Serum bilirubin
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