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
01863 - Leucine-induced hypoglycemia 240800 - - - ABCC8 - -
02935 - Transient neonatal diabetes mellitus 2 610374 - - - ABCC8 - -
01966 hhf1 hypoglycemia, hyperinsulinemic, familial, type 1(HHF-1) 256450 - - - ABCC8 - -
00151 NIDDM diabetes mellitus, noninsulin-dependent (NIDDM) 125853 - - - 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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