Benign conjugated hyperbilirubinemia without hepatic pigment.
- Specialty
- Gastroenterology
- Subspecialty
- Gastroenterology / Hepatology
- Sex & age distribution
- Male: affected; Female: affected, equal; Children: yes
- Gene(s) involved
- SLCO1B1, SLCO1B3
- Alternative names & eponyms
- Rotor-type hyperbilirubinemia
Etiology & mechanism
Complete deficiency of hepatic OATP1B1 and OATP1B3.
Gene(s) involved (2)
Symptoms & signs (4)
In plain terms, someone with Rotor syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
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Shares symptoms with
2 shared
Cold agglutinin syndrome
dark urine, fatigue
2 shared
Dubin–Johnson syndrome
dark urine, mild jaundice
1 shared
Atypical hemolytic uremic syndrome
fatigue
1 shared
Autoimmune polyglandular syndrome type 2
fatigue
1 shared
Barth syndrome
fatigue
1 shared
Camurati–Engelmann syndrome
fatigue
1 shared
Carcinoid heart disease
fatigue
1 shared
Cardiorenal syndrome
fatigue
1 shared
Castleman syndrome
fatigue
1 shared
Cramp-fasciculation syndrome
fatigue
Shares genes with
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