- OMIM ID
-
254210
- OMIM term:
- MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH EPISODIC APNEA
- Alternative terms:
-
CMS-EA
MYASTHENIC SYNDROME, PRESYNAPTIC, CONGENITAL, ASSOCIATED WITH EPISODIC APNEA
CONGENITAL MYASTHENIC SYNDROME TYPE Ia2; CMS1A2
CMS Ia2
MYASTHENIA, FAMILIAL INFANTILE; FIM
MYASTHENIA GRAVIS, FAMILIAL INFANTILE, 2, FORMERLY; FIMG2, FORMERLY
- (∗) Location:
- 10q11.23
- (†) Associated OMIM genes:
- CHAT
- (‡) Associated MGI genes:
Loading mouse genes ...