CHAT congenital myasthenic syndrome
CMS6
CMSEA
FIM
congenital myasthenic syndrome 6
congenital myasthenic syndrome caused by mutation in CHAT
congenital myasthenic syndrome type 6
presynaptic congenital myasthenic syndrome 6
CMS Ia2, formerly
CMS w/episodic apnea
CMS-ea
CMS1A
CMS1A2, formerly
Cms Ia2
Cms Ia2, formerly
FIM, formerly
FIMG2 (formerly)
FIMG2, formerly
congenital myasthenic syndrome type 1a
congenital myasthenic syndrome type Ia
congenital myasthenic syndrome type Ia2, formerly
congenital myasthenic syndrome with episodic apnea
myasthenia familial infantile
myasthenia gravis familial infantile 2 (formerly)
myasthenia gravis, familial infantile, 2
myasthenia gravis, familial infantile, 2, formerly
myasthenia, familial infantile
myasthenia, familial infantile, formerly
myasthenic syndrome congenital associated with episodic apnea
myasthenic syndrome, congenital, 6, presynaptic
myasthenic syndrome, congenital, associated with episodic apnea
myasthenic syndrome, presynaptic, congenital, associated with episodic apnea