All diseases

OMIM ID
608567
OMIM term:
SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE; SSS1
Alternative terms:
SINUS RHYTHM, CONGENITAL ABSENCE OF
SINUS NODE DISEASE, FAMILIAL, AUTOSOMAL RECESSIVE
SICK SINUS SYNDROME, CONGENITAL
SINUS BRADYCARDIA SYNDROME, FAMILIAL
(∗) Location:
3p22.2  
(†) Associated OMIM genes:
SCN5A  
(‡) Associated MGI genes:

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/6nk4fvkj