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visceral heterotaxy
Genetics:
- associated with defects in CFC1 (autosomal type 2)
- associated with defects in NODAL (autosomal type 5)
Clinical manifestations:
- variable
- congenital anomaly
- complex cardiac malformations
- situs inversus or situs ambiguus
- transposition of the great vessels
- ventricular septal defect
- atrial septal defect
- truncuscommunis
- dextrocardia
Specific
visceral heterotaxy X-linked type 1
General
congenital anomaly (birth defect)
genetic syndrome (multisystem disorder)
Database Correlations
OMIM correlations
References
OMIM :accession 270100
OMIM :accession 608808