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Searched for "Jaundice".

53 results found on Genetics Home Reference.

Showing results 1 to 20.
  • Dubin-Johnson syndrome condition summary
    Found in name or synonym: Jaundice, Chronic Idiopathic
    Related genes:
  • Gilbert syndrome condition summary
    Found in name or synonym: familial nonhemolytic jaundice
    Related genes:
  • jaundice definition
  • North American Indian childhood cirrhosis condition summary
    Found: ...skin and whites of the eyes (jaundice) in affected infants. The disorder...
    Related genes:
  • Rotor syndrome condition summary
    Found: ...the skin or whites of the eyes (jaundice). In people with Rotor syndrome,...
    Related genes:
  • Crigler-Najjar syndrome condition summary
    Found: ...skin and whites of the eyes (jaundice). In Crigler-Najjar syndrome, jaundice...
    Related genes:
  • congenital dyserythropoietic anemia condition summary
    Found: ...yellowing of the skin and eyes (jaundice) and an enlarged liver and spleen...
    Related genes:
  • glucose-6-phosphate dehydrogenase deficiency condition summary
    Found: ...skin and whites of the eyes (jaundice), dark urine, fatigue, shortness...
    Related genes:
  • benign recurrent intrahepatic cholestasis condition summary
    Found: ...skin and whites of the eyes (jaundice) a few weeks later. Other general...
    Related genes:
  • progressive familial intrahepatic cholestasis condition summary
    Found: ...skin and whites of the eyes (jaundice), failure to gain weight and grow...
    Related genes:
  • sialuria condition summary
    Found: ...whites of the eyes (neonatal jaundice), an enlarged liver and spleen...
    Related genes:
  • UGT1A1 gene summary
    Official name: UDP glucuronosyltransferase 1 family, polypeptide A1
    Found: Although jaundice is common in newborns, mutations...
  • hereditary spherocytosis condition summary
    Found: ...yellowing of the eyes and skin (jaundice), and an enlarged spleen (splenomegaly)....
    Related genes:
  • SLCO1B1 gene summary
    Official name: solute carrier organic anion transporter family, member 1B1
    Found: ...skin and whites of the eyes (jaundice). For this condition to occur,...
  • SLCO1B3 gene summary
    Official name: solute carrier organic anion transporter family, member 1B3
    Found: ...skin and whites of the eyes (jaundice). For this condition to occur,...
  • pyruvate kinase deficiency condition summary
    Found: ...yellowing of the eyes and skin (jaundice), extreme tiredness (fatigue),...
    Related genes:
  • alpha-1 antitrypsin deficiency condition summary
    Found: ...skin and whites of the eyes (jaundice). Approximately 15 percent of adults...
    Related genes:
  • ABCB11 gene summary
    Official name: ATP-binding cassette, sub-family B (MDR/TAP), member 11
    Found: ...skin and whites of the eyes (jaundice). On occasion, people with BRIC2...
  • ATP8B1 gene summary
    Official name: ATPase, aminophospholipid transporter, class I, type 8B, member 1
    Found: ...skin and whites of the eyes (jaundice). Most ATP8B1 gene mutations that...
  • Wolman disease condition summary
    Found: ...and the whites of the eyes (jaundice), vomiting, diarrhea, developmental...
    Related genes:
 
Published: July 21, 2014