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Atrial stand still
1 OMIM reference -
1 associated gene
14 connected diseases
No signs/symptoms info
Disease Type of connection
Romano-Ward syndrome
Brugada syndrome
Familial atrial fibrillation
Familial isolated dilated cardiomyopathy
Familial progressive cardiac conduction defect
Familial sick sinus syndrome
Idiopathic ventricular fibrillation, not Brugada type
Catecholaminergic polymorphic ventricular tachycardia
Congenital analbuminemia
Autosomal dominant limb-girdle muscular dystrophy type 1C
Rippling muscle disease
Juvenile myelomonocytic leukemia
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
X-linked non-syndromic intellectual deficit
- Atrial cardiomyopathy with heart block

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

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

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
SCN5A Q14524600163
No signs/symptoms info available.