All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05293 EIEE37 encephalopathy, epileptic, early infantile, type 37 (EIEE-37) 616981 AR - - FRRS1L - -
04406 EPM8 epilepsy?, myoclonic, progressive, type 8 (EPM-8) 616230 AR 2 2 CERS1 - -
00151 NIDDM diabetes mellitus, type II (NIDDM) 125853 AD 8 7 ABCC8, AKT2, CDKAL1, ENPP1, GCGR, GCK, GPD2, HMGA1, HNF1A, HNF1B, HNF4A, IGF2BP2, IRS1, IRS2, KCNJ11, LIPC, MAPK8IP1, MTNR1B, NEUROD1, PAX4, 8 more - -
02262 RS1 retinoschisis, type 1, X-linked 312700 XLR 1394 1042 RS1 - -
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