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
05130 CSNB blindness, night, stationary, congenital (CSNB) - - 102 98 LRIT3, RIMS2 - -
03819 CSNB1F blindness, night, stationary, congenital, type 1F (CSNB1F) 615058 AR - - LRIT3 - -
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