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Familial sick sinus syndrome
3 OMIM references -
3 associated genes
18 connected diseases
No signs/symptoms info
Disease Type of connection
Brugada syndrome
Familial isolated dilated cardiomyopathy
Romano-Ward syndrome
Atrial septal defect, ostium secundum type
Atrial stand still
Familial atrial fibrillation
Familial progressive cardiac conduction defect
Idiopathic ventricular fibrillation, not Brugada type
Catecholaminergic polymorphic ventricular tachycardia
Congenital analbuminemia
Autosomal dominant limb-girdle muscular dystrophy type 1C
Chronic myeloid leukemia
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Rippling muscle disease
Juvenile myelomonocytic leukemia
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
X-linked non-syndromic intellectual deficit
Synonym(s):
- Familial sinus node dysfunction
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
3 OMIM references -
1 MeSH reference: D012804
Gene symbol UniProt reference OMIM reference
HCN4 Q9Y3Q4605206
MYH6 P13533160710
SCN5A Q14524600163
No signs/symptoms info available.