All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00296 CTRCT cataract (CTRCT) - - 1189 1162 AGK, BFSP1, BFSP2, CASP7, CRYAA, CRYBA4, CRYGC, CRYGD, FYCO1, GJA3, HSF4, LIM2, MIP, SOLH - -
03705 CTRCT38;CATC5 cataract, type 38 (CTRCT-38, cataract, autosomal recessive congenital 5 (CATC-5)) 614691 AR - - AGK - -
01695 Sengers;MTDPS10 Senger syndrome (mitochondrial DNA depletion syndrome, type 10 (cardiomyopathic type, MTDPS-10)) 212350 AR 1 1 AGK - -
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