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Complete atrioventricular canal - ventricle hypoplasia
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Benign familial chorea
2 OMIM references -
1 associated gene
2 signs/symptoms
Complete atrioventricular canal - ventricle hypoplasia
Benign familial chorea

CRELD1
(UniProt - OMIM)
 NKX2-1
(UniProt - OMIM)
GATA4
(UniProt - OMIM)
GATA6
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
GATA6
(0.72)
NKX2-1


Citations in the biomedical literature:


Complete atrioventricular canal - ventricle hypoplasia
CRELD1 GATA4 GATA6
Benign familial chorea
NKX2-1



Complete atrioventricular canal - ventricle hypoplasia
Benign familial chorea

Synonym(s):
- CAVC - ventricle hypoplasia
- CAVC type B
- Complete atrioventricular canal type B
Synonym(s):
- Hereditary benign chorea
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare surgical cardiac disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
2 OMIM references -
No MeSH references
Benign familial chorea

Very frequent
- Abnormal gait
- Movement disorder



Complete atrioventricular canal - ventricle hypoplasia

(no data available)