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
06217 COXPD31 Combined oxidative phosphorylation deficiency 31 617228 AR - - MIPEP - -
00296 CTRCT cataract (CTRCT) - - 1199 1172 AGK, BFSP1, BFSP2, CASP7, CRYAA, CRYBA4, CRYGC, CRYGD, FYCO1, GJA3, HSF4, LIM2, MIP, SOLH - -
03878 CTRCT15 cataract, type 15, multiple types (CTRCT-15) 615274 AD - - MIP - -
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