Autosomal recessiv
En forekomst af intrahepatisk kolestase, der skyldes en arvelig ændring i individets genom.
Også kendt som
hereditary intrahepatic cholestasis
Omfatter 21 beslægtede undertyper ↓Skjul undertyper ↑
- 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
