Autozomálně recesivní
An instance of intrahepatic cholestasis that is caused by an inherited modification of the individual's genome.
Známé také jako
hereditary intrahepatic cholestasis
Zahrnuje 21 příbuzných podtypů ↓Skrýt podtypy ↑
- benign recurrent intrahepatic cholestasis
- benign recurrent intrahepatic cholestasis type 1
- benign recurrent intrahepatic cholestasis type 2
- cholestasis, intrahepatic, of pregnancy, 1
- cholestasis, intrahepatic, of pregnancy, 3
- cholestasis, progressive familial intrahepatic, 10
- cholestasis, progressive familial intrahepatic, 11
- cholestasis, progressive familial intrahepatic, 12
- cholestasis, progressive familial intrahepatic, 13
- cholestasis, progressive familial intrahepatic, 4
- cholestasis, progressive familial intrahepatic, 5
- cholestasis, progressive familial intrahepatic, 6
- cholestasis, progressive familial intrahepatic, 7, with or without hearing loss
- cholestasis, progressive familial intrahepatic, 8
- cholestasis, progressive familial intrahepatic, 9
- hereditary North American Indian childhood cirrhosis
- MYO5B-related progressive familial intrahepatic cholestasis
- progressive familial intrahepatic cholestasis
- progressive familial intrahepatic cholestasis type 1
- progressive familial intrahepatic cholestasis type 2
- progressive familial intrahepatic cholestasis type 3
