ODCs

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

PROTEIN INTERACTIONS: 1

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

Inherited Creutzfeldt-Jakob disease

Idiopathic ventricular fibrillation, not Brugada type

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


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PRNP	(0.59)	DPP6

Citations in the biomedical literature:

Inherited Creutzfeldt-Jakob disease		Idiopathic ventricular fibrillation, not Brugada type
	Synonym(s): - Inherited CJD		Synonym(s): - Familial paroxysmal ventricular fibrillation, not Brugada type

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

	Classification (ICD10): - Certain infectious and parasitic diseases -		Classification (ICD10): - Diseases of the circulatory system -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.