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Disease Ontology Browser
congenital myasthenic syndrome 1A (DOID:0110663)
Alliance: disease page
Synonyms: CMS1A; CMS IIa; congenital myasthenic syndrome 1A, slow-channel; congenital myasthenic syndrome type IIa
Alt IDs: OMIM:601462
Definition: A congenital myasthenic syndrome characterized by predominantly autosomal dominant inheritance of defects in postsynaptic neuromuscular junctions and early-onset progressive muscle weakness that has_material_basis_in mutation in the CHRNA1 gene on chromosome 2q.

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