All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02940 CSRD;CSNB2B cone-rod synaptic disorder, congenital nonprogressive (CSRD, congenital stationary night blindness, type 2B (CSNB-2B)) 610427 AR - - CABP4 - autosomal recessive
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