All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03453 CSNB1D blindness, night, stationary, congenital, type 1D (CSNB-1D) 613830 - - - SLC24A1 - -
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