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8 OMIM references -
11 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Brugada syndrome
Autosomal dominant limb-girdle muscular dystrophy type 1C

CACNA1C CAV3
CACNB2
GPD1L
HCN4
KCND3
KCNE3
KCNJ8
SCN1B
SCN3B
SCN5A
TRPM4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SCN5A
(0.63)
CAV3



Citations in the biomedical literature:


Brugada syndrome
CACNA1C CACNB2 GPD1L HCN4 KCND3 KCNE3
KCNJ8 SCN1B SCN3B SCN5A TRPM4
Autosomal dominant limb-girdle muscular dystrophy type 1C
CAV3



Brugada syndrome
Autosomal dominant limb-girdle muscular dystrophy type 1C

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

Synonym(s):
- LGMD1C
- Limb-girdle muscular dystrophy due to caveolin-3 deficiency

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: <1 / 1 000 000
Average age onset: childhood
Average age of death: normal
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.