All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02873 CTRCT22;CATCN2 cataract, type 22 (CTRCT-22, cataract congenital nuclear, autosomal recessive 2 CATCN-2)) 609741 AD;AR - - CRYBB3 - -
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