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
02846 CIMT1 carotid intimal medial thickness 1 609338 - - - PPARG - -
05545 FPLD lipodystrophy, familial partial (FPLD) - - 61 61 PPARG - -
02503 FPLD3 lipodystrophy, familial partial, type 3 (FPLD-3) 604367 AD - - PPARG, PPP1R3A - -
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 - -
00259 obesity obesity, susceptibility to (incl. leanness) 601665 AD;AR;Mu 503 72 ADCY3, MC4R, POMC, PPARG - -
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