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Isolated congenitally uncorrected transposition of the great arteries
1 associated gene
11 connected diseases
No signs/symptoms info
Disease Type of connection
Double outlet right ventricle
Situs ambiguus
Acrocallosal syndrome
Greig cephalopolysyndactyly syndrome
Pallister-Hall syndrome
Polysyndactyly, bilateral
Polysyndactyly, unilateral
Postaxial polydactyly type A, bilateral
Postaxial polydactyly type A, unilateral
Postaxial polydactyly type B, bilateral
Postaxial polydactyly type B, unilateral
- Isolated congenitally uncorrected transposition of the great vessels

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare surgical cardiac disease

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
External references:
No OMIM references
No MeSH references

Gene symbol UniProt reference OMIM reference
ZIC3 O60481300265
No signs/symptoms info available.