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Complete atrioventricular canal - ventricle hypoplasia
3 associated genes
No signs/symptoms info
COMMON GENES: 2
Partial atrioventricular canal
2 associated genes
No signs/symptoms info
Complete atrioventricular canal - ventricle hypoplasia
Partial atrioventricular canal

CRELD1
(UniProt - OMIM)
 CRELD1
(UniProt - OMIM)
GATA4
(UniProt - OMIM)
 GATA4
(UniProt - OMIM)
GATA6
(UniProt - OMIM)

COMMON
GENES 		CRELD1
GATA4


Citations in the biomedical literature:


Complete atrioventricular canal - ventricle hypoplasia
CRELD1 GATA4 GATA6
Partial atrioventricular canal



Complete atrioventricular canal - ventricle hypoplasia
Partial atrioventricular canal

Synonym(s):
- CAVC - ventricle hypoplasia
- CAVC type B
- Complete atrioventricular canal type B
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare surgical cardiac disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare surgical cardiac disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
1 MeSH reference: C536112
No signs/symptoms info available.