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Congenital Myasthenic Syndrome 3C

Disease ID: disease_node_14293

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DbxrefMIM:616323
SubclassofDOID_0050737, DOID_3635
Data SourceDOID
Synonymscongenital myasthenic syndrome 3C associated with acetylcholine receptor deficiency
Doid Labelcongenital myasthenic syndrome 3C
Doid DescriptionA congenital myasthenic syndrome characterized by autosomal recessive inheritance of postsynaptic neuromuscular junction defects, low amplitude of the miniature endplate potential and current, and early-onset muscle weakness that has_material_basis_in compound heterozygous mutation in the CHRND gene on chromosome 2q37.
Has SymptomSYMP_0000094
Has Material Basis InGENO_0000148
Disease Node Iddisease_node_14293
Doid IdDOID_0110664
Disease Has Basis InHP_0001197
LabelCongenital Myasthenic Syndrome 3C