All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06906 DEE encephalopathy, developmental and epileptic - - 269 261 ATP1A3, CELF2, DALRD3, DNM1, GAD1, GLUL, GNAO1, KCNA2, KCNH5, NEUROD2, NTRK2, TMEM63B - -
06372 DEE72 encephalopathy, developmental and epileptic, 72 618374 AD - - NEUROD2 - -
05593 MODY diabetes of the young, maturity-onset (MODY) - - 3709 3706 INS, NEUROD1 - -
02584 MODY6 diabetes of the young, maturity-onset, type 6 (MODY6) 606394 - - - NEUROD1 - -
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 - -
00415 PCT porphyria cutanea tarda (PCT) 176100 AD;AR - - HFE, UROD - -
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