Hereditary hyperbilirubinemia
Jump to navigation
Jump to search
| Hereditary hyperbilirubinemia | |
| ICD-10 | E80.4-E80.6 |
|---|---|
| ICD-9 | 277.4 |
| eMedicine | med/1065 med/1066 |
| MeSH | D006933 |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Hereditary hyperbilirubinemia refers to the condition where levels of bilirubin are elevated, for reasons that can be attributed to a metabolic disorder.
An example is Crigler-Najjar syndrome.
External links
- http://www.som.tulane.edu/classware/pathology/medical_pathology/New_for_99/liver_gb/sld017.htm
- Elferink RP, Ottenhoff R, Liefting W, de Haan J, Jansen PL (1989). "Hepatobiliary transport of glutathione and glutathione conjugate in rats with hereditary hyperbilirubinemia". J. Clin. Invest. 84 (2): 476–83. doi:10.1172/JCI114189. PMID 2760197. Unknown parameter
|month=ignored (help)
Template:Purine, pyrimidine, porphyrin, bilirubin metabolic pathology