All diseases

OMIM ID
192500
OMIM term:
LONG QT SYNDROME 1; LQT1
Alternative terms:
WARD-ROMANO SYNDROME; WRS
ROMANO-WARD SYNDROME; RWS
VENTRICULAR FIBRILLATION WITH PROLONGED QT INTERVAL LONG QT SYNDROME 1/2, DIGENIC, INCLUDED; LQT1/2, DIGENIC, INCLUDED
LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO, INCLUDED
(∗) Location:
11p15.5-p15.4  
(†) Associated OMIM genes:
KCNQ1  
(‡) Associated MGI genes:
Kcnq1  

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