Passer au contenu principal

Medical Subject Headings (thesaurus)

Choisissez le vocabulaire dans lequel chercher

aligner
annoter
télécharger

Concept information

Pathological Conditions, Signs and Symptoms > Pathologic Processes > Disease Attributes > Chronic Disease > Jaundice, Chronic Idiopathic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Hyperbilirubinemia, Hereditary > Jaundice, Chronic Idiopathic
Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Hyperbilirubinemia, Hereditary > Jaundice, Chronic Idiopathic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Infant, Newborn, Diseases > Hyperbilirubinemia, Neonatal > Jaundice, Neonatal > Jaundice, Chronic Idiopathic
... > Pathological Conditions, Signs and Symptoms > Pathologic Processes > Hyperbilirubinemia > Hyperbilirubinemia, Neonatal > Jaundice, Neonatal > Jaundice, Chronic Idiopathic

Terme préférentiel

Jaundice, Chronic Idiopathic  

Type

  • mesh:Descriptor

Définition

  • A benign, autosomally recessive inherited hyperbilirubinemia characterized by the presence of a dark pigment in the centrilobular region of the liver cells. There is a functional defect in biliary excretion of bilirubin, cholephilic dyes, and porphyrins. Affected persons may be asymptomatic or have vague constitutional or gastrointestinal symptoms. The liver may be slightly enlarged, and oral and intravenous cholangiography fails to visualize the biliary tract.

Concept générique

Synonyme(s)

  • Dubin-Johnson Syndrome
  • Hyperbilirubinemia 2
  • Hyperbilirubinemia II

Qualificatif(s) autorisé(s)

Traductions

URI

http://data.loterre.fr/ark:/67375/JVR-HH7G89PV-1

Télécharger ce concept :

RDF/XML TURTLE JSON-LD Date de création 01/01/1999, dernière modification le 12/03/2021