Medical Definition of Familial nonhemolytic jaundice

1. Mild jaundice due to increased amounts of unconjugated bilirubin in the plasma without evidence of liver damage, biliary obstruction, or haemolysis; thought to be due to an inborn error of metabolism in which the excretion of bilirubin by the liver is defective, ascribed to decreased conjugation of bilirubin as a glucuronide or impaired uptake of hepatic bilirubin. Synonym: benign familial icterus, constitutional hepatic dysfunction, Gilbert's disease, Gilbert's syndrome, Hebra's disease. (05 Mar 2000)

Lexicographical Neighbors of Familial Nonhemolytic Jaundice

familial hypophosphatemic rickets
familial intestinal polyposis
familial juvenile nephrophthisis
familial lipodystrophy
familial lipoprotein lipase deficiency
familial lipoprotein lipase inhibitor
familial mediterranean fever
familial mental retardation 1
familial mental retardation protein
familial microcytic anaemia
familial multiple endocrine adenomatosis
familial nephrosis
familial neuroviscerolipidosis
familial nonhaemolytic nonobstructive jaundice
familial nonhemolytic jaundice (current term)
familial paroxysmal rhabdomyolysis
familial periodic paralysis
familial polyposis
familial polyposis coli
familial pseudoinflammatory macular degeneration
familial pseudoinflammatory maculopathy
familial pyridoxine-responsive anaemia
familial recurrent polyserositis
familial screening
familial spinal muscular atrophy
familial tremor
familial white folded dysplasia
familiality

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