All diseases

OMIM ID
608931
OMIM term:
MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
Alternative terms:
MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
MYASTHENIC SYNDROME, CONGENITAL, TYPE Id; CMS1D
CMS Id MYASTHENIC SYNDROME, CONGENITAL, WITH FACIAL DYSMORPHISM, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY, INCLUDED
MYASTHENIC SYNDROME, CONGENITAL, Ie, INCLUDED; CMS1E, INCLUDED
CMS Ie, INCLUDED
(∗) Location:
11p11.2   17p13.1   17p13.2   9q31.3  
(†) Associated OMIM genes:
CHRNB1   CHRNE   MUSK   RAPSN  
(‡) Associated MGI genes:
Chrne   Musk  

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