Familial intrahepatic cholestasis
MONDO:0017290An instance of intrahepatic cholestasis that is caused by an inherited modification of the individual's genome.
Also known as: hereditary intrahepatic cholestasis
23 clinical trials for this condition and its sub-types, 1 tagged with Familial intrahepatic cholestasis itself.
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Sub-types of Familial intrahepatic cholestasis
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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
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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