ODCs

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1 OMIM reference -
1 associated gene
3 signs/symptoms

PROTEIN INTERACTIONS: 1

3 associated genes
No signs/symptoms info

Atrial septal defect - atrioventricular conduction defects

Complete atrioventricular canal - ventricle hypoplasia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	NKX2-5	(0.96)	GATA4

Citations in the biomedical literature:

Atrial septal defect - atrioventricular conduction defects		Complete atrioventricular canal - ventricle hypoplasia
	Synonym(s): (no synonyms)		Synonym(s): - CAVC - ventricle hypoplasia - CAVC type B - Complete atrioventricular canal type B

	Classification (Orphanet): - Rare cardiac disease - Rare developmental defect during embryogenesis - Rare genetic disease - 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: Class of prevalence: <1 / 1 000 000 Average age onset: no data available Average age of death: no data available Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 1 OMIM reference - No MeSH references		External references: No OMIM references No MeSH references

Atrial septal defect - atrioventricular conduction defects
	Very frequent - Autosomal dominant inheritance - Cardiac conduction defect / sinoauricular / heart / auriculoventricular / branch block - Cardiac septal defect
Complete atrioventricular canal - ventricle hypoplasia
(no data available)