Alstrom Syndrome, Bardet Biedl Syndrome, Retinitis Pigmentosa,Leber Congenital Amaurosis, Meckel Syndrome
Obesity, Leptin Deficiency, Leptin Receptor Deficiency. Genes- ADCY3, ALMS1, ARL6, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, CEP290, CRTC1, CUL4B, DYRK1B, GNAS, KSR2, LEP, LEPR, MAGEL2, MC3R, MC4R, MKKS, MKS1, NR0B2, NTRK2, PCSK1, PHF6, POMC, PPARG, PYY, SDCCAG8, SIM1, TRIM32, TTC8, UCP3, VPS13B, WDPCP