Also Known As
CHAT congenital myasthenic syndromeCMS Ia2CMS1A2CMS6CMSEAFIMFIMG2congenital myasthenic syndrome 6congenital myasthenic syndrome 6, presynapticcongenital myasthenic syndrome caused by mutation in CHATcongenital myasthenic syndrome type 6congenital myasthenic syndrome type Ia2congenital presynaptic myasthenic syndrome associated with episodic apneafamilial infantile myastheniafamilial infantile myasthenia gravis 2presynaptic congenital myasthenic syndrome 6CMS Ia2, formerlyCMS w/episodic apneaCMS-eaCMS1ACMS1A2, formerlyCms Ia2Cms Ia2, formerlyFIM, formerlyFIMG2 (formerly)FIMG2, formerlycongenital myasthenic syndrome type 1acongenital myasthenic syndrome type Iacongenital myasthenic syndrome type Ia2, formerlycongenital myasthenic syndrome with episodic apneamyasthenia familial infantilemyasthenia gravis familial infantile 2 (formerly)myasthenia gravis, familial infantile, 2myasthenia gravis, familial infantile, 2, formerlymyasthenia, familial infantilemyasthenia, familial infantile, formerlymyasthenic syndrome congenital associated with episodic apneamyasthenic syndrome, congenital, 6, presynapticmyasthenic syndrome, congenital, associated with episodic apneamyasthenic syndrome, presynaptic, congenital, associated with episodic apnea