ODCs

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5 OMIM references -
4 associated genes
1 sign/symptom

PROTEIN INTERACTIONS: 1

2 associated genes
No signs/symptoms info

Familial progressive cardiac conduction defect

Complete atrioventricular canal - left heart obstruction


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

Citations in the biomedical literature:

Familial progressive cardiac conduction defect		Complete atrioventricular canal - left heart obstruction
	Synonym(s): - Familial LenÃ¨gre disease - Familial Lev disease - Familial Lev-LenÃ¨gre disease - Familial PCCD - Familial progressive heart block - Hereditary bundle branch defect		Synonym(s): - CAVC - left heart obstruction - CAVC type A - Complete atrioventricular canal type A

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

	Classification (ICD10): - Diseases of the circulatory system -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: elderly Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 5 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

Familial progressive cardiac conduction defect
	Frequent - Cardiac rhythm disorder / arrhythmia
Complete atrioventricular canal - left heart obstruction
(no data available)