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Results 1 - 6 of 6 for Hyperbilirubinemia
  1. Crigler-Najjar syndrome 
    ... a toxic substance called bilirubin in the blood (hyperbilirubinemia). Bilirubin is produced when red blood cells are ... buildup of unconjugated bilirubin in their blood (unconjugated hyperbilirubinemia).Bilirubin has an orange-yellow tint, and hyperbilirubinemia ...
    https://medlineplus.gov/genetics/condition/crigler-najjar-syndrome - Genetics
  2. Gilbert syndrome 
    ... a toxic substance called bilirubin in the blood (hyperbilirubinemia). Bilirubin, which has an orange-yellow tint, is ... buildup of unconjugated bilirubin in their blood (unconjugated hyperbilirubinemia). In affected individuals, bilirubin levels fluctuate and very ...
    https://medlineplus.gov/genetics/condition/gilbert-syndrome - Genetics
  3. Rotor syndrome 
    ... of a substance called bilirubin in the blood (hyperbilirubinemia). Bilirubin is produced when red blood cells are ... not show signs and symptoms of the condition. Hyperbilirubinemia, Rotor type Genetic Testing Registry: Rotor syndrome Rotor ...
    https://medlineplus.gov/genetics/condition/rotor-syndrome - Genetics
  4. Dubin-Johnson syndrome 
    ... accumulates in the body, causing a condition called hyperbilirubinemia. The buildup of bilirubin in the body causes ... jaundice with pigmented liver DJS Dubin-Sprinz syndrome Hyperbilirubinemia II Hyperbilirubinemia, Dubin-Johnson type Jaundice, chronic idiopathic ...
    https://medlineplus.gov/genetics/condition/dubin-johnson-syndrome - Genetics
  5. Glucose-6-phosphate dehydrogenase deficiency 
    Glucose-6-phosphate dehydrogenase deficiency is a genetic disorder that affects red blood cells, which carry oxygen from the lungs to tissues throughout the ...
    https://medlineplus.gov/...cose-6-phosphate-dehydrogenase-deficiency - Genetics
  6. Proopiomelanocortin deficiency 
    ... a toxic substance called bilirubin in the blood (hyperbilirubinemia), and a reduced ability to produce and release ...
    https://medlineplus.gov/.../condition/proopiomelanocortin-deficiency - Genetics