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Benign recurrent intrahepatic cholestasis type 2
1 OMIM reference -
1 associated gene
3 connected diseases
No signs/symptoms info
Disease Type of connection
Intrahepatic cholestasis of pregnancy
Progressive familial intrahepatic cholestasis type 2
Kostmann syndrome
Synonym(s):
- BRIC type 2
- BRIC2
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hepatic disease
Classification (ICD10):
- Diseases of the digestive system -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
ABCB11 O95342603201
No signs/symptoms info available.