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The purpose of the registry is to know the status of primary biliary colgantis, autoimmune hepatitis, primary sclerosing cholagitis and genetic cholestatic diseases in Spain.
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| Measure | Description | Time Frame |
|---|---|---|
| Prevalence and characteristics of autoimmune and cholestatic liver disease in Spain | Evaluation of clinical characteristics of autoimmune and cholestatic liver diseases | 2025 |
| Measure | Description | Time Frame |
|---|---|---|
| Development of liver-related events in autoimmune ahd cholestatic liver diseases | 2025 | |
| Treatment of autoimmune and cholestatic liver diseases in Spain | 2016-2030 |
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Inclusion Criteria:
Exclusion Criteria:
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Patients with a confirmed diagnosis for PBC, HAI, PSC or any genetic cholestasis
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Asociación Española para el Estudio del Hígado Asociación Espa | Contact | 0034915551119 | registrocolhay@gmail.com |
| Name | Affiliation | Role |
|---|---|---|
| Maria Carlota Londoño Londoño | Asociación Española para el Estudio del Hígado | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hospital Clinic | Recruiting | Barcelona | Spain |
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| ID | Term |
|---|---|
| D008105 | Liver Cirrhosis, Biliary |
| D015209 | Cholangitis, Sclerosing |
| D016738 | Alagille Syndrome |
| D006933 | Hyperbilirubinemia, Hereditary |
| D007566 | Jaundice, Chronic Idiopathic |
| D030342 | Genetic Diseases, Inborn |
| ID | Term |
|---|---|
| D002780 | Cholestasis, Intrahepatic |
| D002779 | Cholestasis |
| D001649 | Bile Duct Diseases |
| D001660 | Biliary Tract Diseases |
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| D004066 |
| Digestive System Diseases |
| D008107 | Liver Diseases |
| D008103 | Liver Cirrhosis |
| D005355 | Fibrosis |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D002761 | Cholangitis |
| D006330 | Heart Defects, Congenital |
| D018376 | Cardiovascular Abnormalities |
| D002318 | Cardiovascular Diseases |
| D000015 | Abnormalities, Multiple |
| D000013 | Congenital Abnormalities |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D008661 | Metabolism, Inborn Errors |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D007567 | Jaundice, Neonatal |
| D051556 | Hyperbilirubinemia, Neonatal |
| D007232 | Infant, Newborn, Diseases |
| D002908 | Chronic Disease |
| D020969 | Disease Attributes |