Cytoscape Web
Click node...

Biliary atresia with splenic malformation syndrome
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Situs ambiguus
6 associated genes
No signs/symptoms info
Biliary atresia with splenic malformation syndrome
Situs ambiguus

CFC1
(UniProt - OMIM)
 ACVR2B
(UniProt - OMIM)
CCDC11
(UniProt - OMIM)
CFC1
(UniProt - OMIM)
LEFTY2
(UniProt - OMIM)
NODAL
(UniProt - OMIM)
ZIC3
(UniProt - OMIM)

COMMON
GENES 		CFC1


Citations in the biomedical literature:


Biliary atresia with splenic malformation syndrome
CFC1
Situs ambiguus
ACVR2B CCDC11 LEFTY2 NODAL ZIC3



Biliary atresia with splenic malformation syndrome
Situs ambiguus

Synonym(s):
- BASM syndrome
Synonym(s):
- Incomplete situs inversus
- Partial situs inversus
- Situs ambiguous
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare hepatic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare surgical cardiac disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: multigenic/multifactorial
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.