Inborn disorder of bilirubin metabolism

MONDO:0017755

An instance of bilirubin metabolism disease that is caused by an inherited modification of the individual's genome.

Also known as: disorder of bilirubin metabolism, disorder of bilirubin metabolism and excretion, hereditary bilirubin metabolism disease, inborn disorder of bilirubin metabolism and excretion, bilirubin metabolism disorder

39 clinical trials for this condition and its sub-types, 0 tagged with Inborn disorder of bilirubin metabolism itself.

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Where it sits in the disease tree

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Part of

↑ Inborn disorder of porphyrin metabolism (63) ↑ Bilirubin metabolism disease (48)

Sub-types of Inborn disorder of bilirubin metabolism

Hereditary hyperbilirubinemia 0 trials · 18 incl. sub-types
7 sub-types
- Transient familial neonatal hyperbilirubinemia 18 trials
- Crigler-Najjar syndrome 0 trials Sub-types →
- Dubin-Johnson syndrome 0 trials
- Gilbert syndrome 0 trials
- Rotor syndrome 0 trials
- Hyperbilirubinemia, conjugated, type 3 0 trials
- Hyperbilirubinemia, shunt, primary 0 trials
Progressive familial intrahepatic cholestasis 16 trials · 17 incl. sub-types
16 sub-types
- Progressive familial intrahepatic cholestasis type 1 4 trials
- Progressive familial intrahepatic cholestasis type 2 4 trials
- Cholestasis, progressive familial intrahepatic, 4 2 trials
- Progressive familial intrahepatic cholestasis type 3 2 trials
- Cholestasis, progressive familial intrahepatic, 5 1 trial
- Cholestasis, progressive familial intrahepatic, 6 1 trial
- Hereditary North American Indian childhood cirrhosis 1 trial
- MYO5B-related progressive familial intrahepatic cholestasis 0 trials
- Benign recurrent intrahepatic cholestasis type 1 0 trials
- Cholestasis, progressive familial intrahepatic, 10 0 trials
- Cholestasis, progressive familial intrahepatic, 11 0 trials
- Cholestasis, progressive familial intrahepatic, 12 0 trials
- Cholestasis, progressive familial intrahepatic, 13 0 trials
- Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss 0 trials
- Cholestasis, progressive familial intrahepatic, 8 0 trials
- Cholestasis, progressive familial intrahepatic, 9 0 trials
Benign recurrent intrahepatic cholestasis 2 trials · 5 incl. sub-types
2 sub-types
- Benign recurrent intrahepatic cholestasis type 2 0 trials · 4 incl. sub-types Sub-types →
- Benign recurrent intrahepatic cholestasis type 1 0 trials
Bilirubin encephalopathy 3 trials
1 sub-type
- Kernicterus due to isoimmunization 0 trials
Arthrogryposis-renal dysfunction-cholestasis syndrome 1 trial
2 sub-types
- Arthrogryposis, renal dysfunction, and cholestasis 1 0 trials
- Arthrogryposis, renal dysfunction, and cholestasis 2 0 trials

Most studied deeper sub-types

Crigler-Najjar syndrome type 1 (0) Crigler-Najjar syndrome type 2 (0)

Including sub-types (39) Tagged with Inborn disorder of bilirubin metabolism (0)

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