Progressive Familial Intrahepatic Cholestasis
Disease ID: disease_node_17766
Connections displayed (default: 10).
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| Dbxref | MIM:PS211600, NCI:C84453, ORDO:172, SNOMEDCT_US_2023_03_01:74162007, UMLS_CUI:C0268312 |
|---|---|
| Subclassof | DOID_1852 |
| Data Source | DOID |
| Synonyms | Byler disease, PFIC |
| Doid Label | progressive familial intrahepatic cholestasis |
| Doid Description | An intrahepatic cholestasis characterized by early onset of chronic unremitting cholestasis of hepatocellular origin that progresses to hepatic fibrosis, cirrhosis, and end-stage liver disease before adulthood. |
| Disease Node Id | disease_node_17766 |
| Doid Id | DOID_0070221 |
| Label | Progressive Familial Intrahepatic Cholestasis |
- Incoming r'ship
SUBCLASS_OFto/from Progressive Familial Intrahepatic Cholestasis 5(ID:disease_node_17767) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Progressive Familial Intrahepatic Cholestasis 4(ID:disease_node_17768) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Cholestasis, Intrahepatic(ID:disease_node_2058) (Disease)