All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03339 FGQTL5 Fasting plasma glucose level quantitative trait locus 5 613463 - - - GCKR - -
02429 HHF3 hypoglycemia, hyperinsulinemic, familial, type 3 (HHF-3) 602485 AD 2 2 GCK - autosomal dominant
01286 MODY2 diabetes of the young, maturity-onset, type 2 (MODY-2) 125851 AD 25 23 GCK - -
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 - -
05783 PNDM1 diabetes mellitus, permanent neonatal, type 1 (PNDM1) 606176 AR 1 1 GCK - -
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