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Search Results
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
- Gilbert syndrome condition summary
Found in name or synonym: familial nonhemolytic jaundice
- jaundice definition
- North American Indian childhood cirrhosis condition summary
Found: ...skin and whites of the eyes (jaundice) in affected infants. The disorder...
- Rotor syndrome condition summary
Found: ...the skin or whites of the eyes (jaundice). In people with Rotor syndrome,...
- UGT1A1 gene summary
Official name: UDP glucuronosyltransferase 1 family, polypeptide A1
Found: Although jaundice is common in newborns, mutations...
- Crigler-Najjar syndrome condition summary
Found: ...skin and whites of the eyes (jaundice). In Crigler-Najjar syndrome, jaundice...
- congenital dyserythropoietic anemia condition summary
Found: ...yellowing of the skin and eyes (jaundice) and an enlarged liver and spleen...
- glucose-6-phosphate dehydrogenase deficiency condition summary
Found: ...skin and whites of the eyes (jaundice), dark urine, fatigue, shortness...
- benign recurrent intrahepatic cholestasis condition summary
Found: ...skin and whites of the eyes (jaundice) a few weeks later. Other general...
- progressive familial intrahepatic cholestasis condition summary
Found: ...skin and whites of the eyes (jaundice), failure to gain weight and grow...
- sialuria condition summary
Found: ...whites of the eyes (neonatal jaundice), an enlarged liver and spleen...
- hereditary spherocytosis condition summary
Found: ...yellowing of the eyes and skin (jaundice), and an enlarged spleen (splenomegaly)....
- 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,...
- 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,...
- pyruvate kinase deficiency condition summary
Found: ...yellowing of the eyes and skin (jaundice), extreme tiredness (fatigue),...
- alpha-1 antitrypsin deficiency condition summary
Found: ...skin and whites of the eyes (jaundice). Approximately 15 percent of adults...
- 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...
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