Syndromes with the highest number of associated genes are Kallmann (ANOS1, CHD7, DUSP6, FEZF1, FGF17, FGF8, FGFR1, FLRT3, FSHB, GNRH1, GNRHR, HS6ST1, IL17RD, KISS1, KISS1R, LHB, NDNF, NSMF, PROK2, PROKR2, SEMA3A, SPRY4, TAC3, TACR3, WDR11) and Noonan syndrome (PTPN11, KRAS, SOS1, RAF1, NRAS, BRAF, LZTR1, SOS2, and RIT1). The gene discussed is ANOS1; the disease is Noonan syndrome.