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MIM:616040 - MYASTHENIC SYNDROME, CONGENITAL, 7A, PRESYNAPTIC, AND DISTAL MOTOR NEUROPATHY, AUTOSOMAL DOMINANT; CMS7A
Xenbase Genes: syt2
Human Disease Resource: MIM
MONDO:0014468 - congenital myasthenic syndrome 7 |
MONDO:0018940 - congenital myasthenic syndrome |
MONDO:0020345 - obsolete presynaptic congenital myasthenic syndrome |