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
00296 CTRCT cataract (CTRCT) - - 948 921 AGK, BFSP1, BFSP2, CASP7, CRYAA, CRYBA4, CRYGC, CRYGD, FYCO1, GJA3, HSF4, LIM2, MIP, SOLH - -
02891 CTRCT18;CATC2 cataract, type 18 (CTRCT-18, cataract, autosomal recessive congenital 2 (CATC-2)) 610019 AR - - FYCO1 - -
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