All diseases

17 entries on 1 page. Showing entries 1 - 17.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03042 - acidosis, tubular, renal, distal, with hemolytic anemia 611590 AR - - SLC4A1 - -
01720 CDPD dystrophy, corneal, endothelial, and perceptive deafness 217400 AR - - SLC4A11 - -
06326 CHC cryohydrocytosis 185020 AD - - SLC4A1 - -
01721 CHED dystrophy, corneal, endothelial 217700 AR 46 16 SLC4A11 - autosomal recessive
01195 DI blood group system, Diego system 110500 - - - SLC4A1 - -
03296 FECD4 dystrophy, corneal, Fuchs endothelial, type 4 613268 - - - SLC4A11 - -
02374 FR blood group system, Froese 601551 - - - SLC4A1 - -
00309 MLRS malaria, susceptibility to 611162 - 3 1 CD36, CISH, CR1, DARC, FCGR2A, FCGR2B, G6PD, GYPA, GYPB, GYPC, HBB, ICAM1, NOS2, SLC4A1, TIRAP, TNF - -
05611 NDD neurodevelopmental disorder (NDD) - - 3531 3346 ACBD6, ADARB1, AP1G1, ARFGEF1, ATP9A, CAMSAP1, CAPRIN1, CASP2, CHASERR, CPSF3L, DDB1, DENND5B, DHX30, DHX9, DOHH, DOT1L, EEFSEC, EIF2C1, EIF2C2, EIF4A2, 70 more - -
07142 NEDHBA neurodevelopmental disorder with hypotonia and characteristic brain abnormalities 620746 AR - - SLC4A10 - -
01539 RTADD acidosis, tubular, renal, distal, autosomal dominant (RTADD) 179800 AD - - SLC4A1 - -
05872 SAO ovalocytosis, South Asian type (SAO) 166900 AD 1 - SLC4A1 - -
05833 SPH spherocytosis (SPH) - - 2 2 ANK1, EPB42, SLC4A1, SPTB - -
03174 SPH4 spherocytosis, type 4 (SPH4) 612653 AD 8 - 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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