All diseases

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2 entries on 1 page. Showing entries 1 - 2.

ID	Abbreviation	Name	OMIM ID	Individuals	Phenotypes	Associated with genes	Associated tissues	Disease features
00114	601665	Obesity, autosomal dominant, 601665 (3)	601665	0	0	, ADRB2, ADRB3, AGRP, CARTPT, ENPP1, GHRL, KANK1, LEPR, MC4R, more than 10, MRAP2, MT-CYB, NR0B2, POMC, PPARG, PPARGC1B, PYY, SDC3, SIM1, UCP1, UCP3	-	-
00102	NIDDM	Diabetes mellitus, noninsulin-dependent, 125853 (3)	125853	0	0	ABCC8, AKT2, CAPN10, CDKAL1, ENPP1, GCGR, GCK, GPD2, HMGA1, HNF1A, HNF1B, HNF4A, IGF2BP2, IL6, INSR, IRS1, IRS2, KCNJ11, LIPC, MAPK8IP1, 13 more	-	-