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Biliary atresia with splenic malformation syndrome
1 associated gene
2 connected diseases
No signs/symptoms info
Disease Type of connection
Double outlet right ventricle
Situs ambiguus
Synonym(s):
- BASM syndrome
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare hepatic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: multigenic/multifactorial
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
CFC1 P0CG37605194
No signs/symptoms info available.