All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04489 CSNB1G blindness, night, stationary, congenital, type 1G (CSNB-1G) 616389 AR - - GNAT1 - -
02942 CSNBAD3 blindness, night, stationary, congenital, autosomal dominant, type 3 (CSNBAD-3) 610444 AD - - GNAT1 - -
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