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HYPERBILIRUBINEMIA, ROTOR TYPE, DIGENIC

MedGen UID:
865342
•Concept ID:
C4016905
•
Finding
OMIM®: 604843; 605495

Recent clinical studies

Diagnosis

Dual hereditary jaundice: simultaneous occurrence of mutations causing Gilbert's and Dubin-Johnson syndrome.
Cebecauerova D, Jirasek T, Budisova L, Mandys V, Volf V, Novotna Z, Subhanova I, Hrebicek M, Elleder M, Jirsa M
Gastroenterology 2005 Jul;129(1):315-20. doi: 10.1053/j.gastro.2004.10.009. PMID: 16012956

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