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) - - 380 362 CASP7, CRYBA4, CRYGC, FYCO1, GJA3, HSF4, LIM2, MIP, SOLH - -
02939 CTRCT23 cataract, type 23 (CTRCT-23, lamellar) 610425 - - - CRYBA4 - -
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