Progressive familial intrahepatic cholestasis type 2 (Q54492)
From determinar.ia.br - Determine suas informações
Progressive familial intrahepatic cholestasis type 2 (PFIC2), a type of progressive familial intrahepatic cholestasis (PFIC), is a severe, neonatal, hereditary disorder in bile formation that is hepatocellular in origin and not associated with extrahepatic features. Initially, PFIC2 was reported under the name Byler syndrome.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1168921980 |
||
| English | Progressive familial intrahepatic cholestasis type 2 |
Progressive familial intrahepatic cholestasis type 2 (PFIC2), a type of progressive familial intrahepatic cholestasis (PFIC), is a severe, neonatal, hereditary disorder in bile formation that is hepatocellular in origin and not associated with extrahepatic features. Initially, PFIC2 was reported under the name Byler syndrome. |
Statements
CID11:ID_1168921980
0 references
