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
05408 FAME epilepsy, myoclonic, familial adult (FAME) - - 69 68 CTNND2, MARCH6, RAPGEF2, SAMD12, STARD7, TNRC6A, YEATS2 - autosomal dominant; myoclonic tremor (cortical tremor), infrequent epilepsy with benign clinical course
05589 FAME6;FMCTE6 epilepsy, myoclonic, familial adult, type 6 (FAME6, FMCTE6) 618074 AD - - TNRC6A - -
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 - -
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