Bilirubin metabolism disease
MONDO:0024431Also known as: disorder of bilirubin metabolism
48 clinical trials for this condition and its sub-types, 0 tagged with Bilirubin metabolism disease itself.
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Sub-types of Bilirubin metabolism disease
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Inborn disorder of bilirubin metabolism 0 trials · 39 incl. sub-types
5 sub-types
- Hereditary hyperbilirubinemia 0 trials · 18 incl. sub-types Sub-types →
- Progressive familial intrahepatic cholestasis 16 trials · 17 incl. sub-types Sub-types →
- Benign recurrent intrahepatic cholestasis 2 trials · 5 incl. sub-types Sub-types →
- Bilirubin encephalopathy 3 trials Sub-types →
- Arthrogryposis-renal dysfunction-cholestasis syndrome 1 trial Sub-types →
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Hyperbilirubinemia 28 trials
2 sub-types
- Hereditary hyperbilirubinemia 0 trials · 18 incl. sub-types Sub-types →
- Neonatal jaundice due to ABO incompatibility 1 trial
Most studied deeper sub-types
Transient familial neonatal hyperbilirubinemia
(18)
Progressive familial intrahepatic cholestasis type 1
(4)
Progressive familial intrahepatic cholestasis type 2
(4)
Cholestasis, progressive familial intrahepatic, 4
(2)
Progressive familial intrahepatic cholestasis type 3
(2)
Cholestasis, progressive familial intrahepatic, 5
(1)
Cholestasis, progressive familial intrahepatic, 6
(1)
Hereditary North American Indian childhood cirrhosis
(1)
Arthrogryposis, renal dysfunction, and cholestasis 1
(0)
Arthrogryposis, renal dysfunction, and cholestasis 2
(0)
Benign recurrent intrahepatic cholestasis type 1
(0)
Benign recurrent intrahepatic cholestasis type 2
(0)
Cholestasis, progressive familial intrahepatic, 10
(0)
Cholestasis, progressive familial intrahepatic, 11
(0)
Cholestasis, progressive familial intrahepatic, 12
(0)
Cholestasis, progressive familial intrahepatic, 13
(0)
Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss
(0)
Cholestasis, progressive familial intrahepatic, 8
(0)
Cholestasis, progressive familial intrahepatic, 9
(0)
Crigler-Najjar syndrome
(0)