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Partial atrioventricular canal

2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Familial progressive cardiac conduction defect

5 OMIM references -
4 associated genes
1 sign/symptom

Partial atrioventricular canal

Familial progressive cardiac conduction defect

CRELD1	(UniProt - OMIM)		NKX2-5	(UniProt - OMIM)
GATA4	(UniProt - OMIM)		SCN1B	(UniProt - OMIM)
			SCN5A	(UniProt - OMIM)
			TRPM4	(UniProt - OMIM)


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

Citations in the biomedical literature:

Partial atrioventricular canal		Familial progressive cardiac conduction defect
	Synonym(s): (no synonyms)		Synonym(s): - Familial LenÃ¨gre disease - Familial Lev disease - Familial Lev-LenÃ¨gre disease - Familial PCCD - Familial progressive heart block - Hereditary bundle branch defect

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

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

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

	External references: No OMIM references 1 MeSH reference: C536112		External references: 5 OMIM references - No MeSH references

Familial progressive cardiac conduction defect
	Frequent - Cardiac rhythm disorder / arrhythmia
Partial atrioventricular canal
(no data available)