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congenital myasthenic syndrome 13 (DOID:0110676)
Alliance: disease page
Synonyms: CMS13; CMSTA2; congenital myasthenic syndrome 13 with tubular aggregates; congenital myasthenic syndrome with tubular aggregates 2
Alt IDs: OMIM:614750
Definition: A congenital myasthenic syndrome characterized by autosomal recessive inheritance of proximal muscle weakness, decremental response to repeated nerve stimulation in EMG studies, and favorable response to acetylcholinesterase inhibitors that has_material_basis_in compound heterozygous mutation in the DPAGT1 gene on chromosome 11q23.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.21
The Jackson Laboratory