ODCs

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2 OMIM references -
2 associated genes
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Idiopathic ventricular fibrillation, not Brugada type

Atrial stand still

DPP6	(UniProt - OMIM)		SCN5A	(UniProt - OMIM)
SCN5A	(UniProt - OMIM)

Citations in the biomedical literature:

Idiopathic ventricular fibrillation, not Brugada type		Atrial stand still
	Synonym(s): - Familial paroxysmal ventricular fibrillation, not Brugada type		Synonym(s): - Atrial cardiomyopathy with heart block

	Classification (Orphanet): - Rare cardiac disease - Rare genetic disease		Classification (Orphanet): - Rare cardiac disease - Rare genetic disease

	Classification (ICD10): - Diseases of the circulatory system -		Classification (ICD10): - Diseases of the circulatory system -

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.