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8 OMIM references -
11 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
6 associated genes
No signs/symptoms info
Brugada syndrome
Behavioral variant of frontotemporal dementia

CACNA1C C9ORF72
CACNB2 CHMP2B
GPD1L GRN
HCN4 MAPT
KCND3 PSEN1
KCNE3 VCP
KCNJ8
SCN1B
SCN3B
SCN5A
TRPM4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CACNA1C
(0.63)
VCP



Citations in the biomedical literature:


Brugada syndrome
CACNA1C CACNB2 GPD1L HCN4 KCND3 KCNE3
KCNJ8 SCN1B SCN3B SCN5A TRPM4
Behavioral variant of frontotemporal dementia
C9ORF72 CHMP2B GRN MAPT PSEN1 VCP



Brugada syndrome
Behavioral variant of frontotemporal dementia

Synonym(s):
- Bangungut
- Dream disease
- Idiopathic ventricular fibrillation, Brugada type
- Pokkuri death syndrome
- SUNDS
- Sudden unexplained nocturnal death syndrome

Synonym(s):
- bv-FTD

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

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

Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: elderly
Type of inheritance: autosomal dominant

External references:
8 OMIM references -
1 MeSH reference: D053840
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.