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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
Fatal familial insomnia
Idiopathic ventricular fibrillation, not Brugada type

PRNP DPP6
SCN5A


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Fatal familial insomnia
PRNP
Idiopathic ventricular fibrillation, not Brugada type
DPP6 SCN5A



Fatal familial insomnia
Idiopathic ventricular fibrillation, not Brugada type

Synonym(s):
(no synonyms)

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:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: D034062
External references:
2 OMIM references -
No MeSH references

No signs/symptoms info available.