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
01966 HHF1 hypoglycemia, hyperinsulinemic, familial, type 1(HHF-1) 256450 AD;AR 17 17 ABCC8 - -
01863 LIH Hypoglycemia of infancy, leucine-sensitive 240800 AD 0 0 ABCC8 - -
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 - -
06157 PNDM3 Diabetes mellitus, permanent neonatal 3, with or without neurologic features 618857 - 0 0 ABCC8 - -
05615 TNDM diabetes mellitus, transient neonatal (TNDM) - - 0 0 ABCC8, KCNJ11, PLAGL1 - -
02935 TNDM2 diabetes mellitus, transient neonatal, type 2 (TNMD-2) 610374 - 0 0 ABCC8 - -
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