Familial cirrhosis
MeSH: C566123ORPHA: 209919
Overview
congenital disorder of digestive system
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with Familial cirrhosis, sourced from HPO and Orphanet clinical annotations.
CirrhosisCopper accumulation in liverHepatic steatosisIncreased urinary copper concentrationIncreased circulating copper concentration
Classification & Codes
MeSH Code
C566123Orphanet Code
ORPHA:209919Familial cirrhosis
| MeSH | C566123 |
| Orphanet | ORPHA:209919 |
| Treatments | 0 drug(s) |
| Symptoms on record | 5 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO