All diseases

OMIM ID
113900
OMIM term:
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA; PFHB1A
Alternative terms:
PFHBIA
HEART BLOCK, PROGRESSIVE FAMILIAL, TYPE I; PFHBI
LENEGRE-LEV DISEASE
CARDIAC CONDUCTION DEFECT, PROGRESSIVE; PCCD
BUNDLE BRANCH BLOCK
HEREDITARY BUNDLE BRANCH SYSTEM DEFECT; HBBD HEART BLOCK, NONPROGRESSIVE, INCLUDED
CARDIAC CONDUCTION DEFECT, NONPROGRESSIVE, INCLUDED
(∗) Location:
3p22.2  
(†) Associated OMIM genes:
SCN5A  
(‡) Associated MGI genes:
Scn5a  

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