All diseases

12 entries on 1 page. Showing entries 1 - 12.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01195 - blood group system, Diego system 110500 - - - SLC4A1 - -
01720 - dystrophy, corneal, and perceptive deafness 217400 - - - SLC4A11 - -
01721 - dystrophy, corneal, endothelial, type 2 217700 - - - SLC4A11 - -
02374 - blood group system, Froese 601551 - - - SLC4A1 - -
03042 - acidosis, tubular, renal, distal, with hemolytic anemia 611590 - - - SLC4A1 - -
03296 FECD-4 dystrophy, corneal, Fuchs endothelial, type 4 (FECD-4) 613268 - - - SLC4A11 - -
00309 MLRS malaria, susceptibility to, resistance (MLRS) 611162 - - - CD36, CISH, CR1, FCGR2A, FCGR2B, G6PD, GYPA, GYPB, GYPC, HBB, ICAM1, NOS2, SLC4A1, TIRAP, TNF - -
01539 RTADD acidosis, tubular, renal, distal, autosomal dominant (RTADD) 179800 - - - SLC4A1 - -
03174 SPH-4 spherocytosis, type 4 (SPH-4) 612653 - - - SLC4A1 - -
02373 SW blood group system, Swann system (SW) 601550 - - - SLC4A1 - -
01208 WD blood group system, Waldner type (WD) 112010 - - - SLC4A1 - -
01209 WR blood group system, Wright antigen (WR) 112050 - - - SLC4A1 - -
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