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TermP valueIC# diseasesdiseases# genesgenes
Neuroactive ligand-receptor interaction0.03420673.6913

CONGENITAL MYASTHENIC SYNDROME 1B, FAST-CHANNEL, HYPOGONADOTROPIC HYPOGONADISM 7 WITHOUT ANOSMIA, MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY, LARON DWARFISM, HYPOTHRYOIDISM, CONGENITAL, NONGOITROUS 4, THYROTROPIN-RELEASING HORMONE DEFICIENCY, ?GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES, HYPOGONADOTROPIC HYPOGONADISM 23 WITH OR WITHOUT ANOSMIA, SCHWARTZ-JAMPEL SYNDROME, TYPE 1, COSTELLO SYNDROME, CONGENITAL MYOPATHY WITH EXCESS OF MUSCLE SPINDLES, MELNICK-NEEDLES SYNDROME, MYHRE SYNDROME, HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6

15

THRA, GNRHR, TSHB, CHRNE, MUSK, LHB, CHRNA1, HSPG2, SMAD4, TRH, HRAS, CHRND, IGF2, FLNA, GHR