All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

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 - -