Disease #03835 (CMS-8 (myasthenic syndrome, congenital, type 8, with pre- and postsynaptic defects (CMS-8)), OMIM:615120)

Official abbreviation CMS-8
Name myasthenic syndrome, congenital, type 8, with pre- and postsynaptic defects (CMS-8)
OMIM ID 615120
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene AGRN
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Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A