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DO Term : congenital myasthenic syndrome 3A [DOID:0110666] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A congenital myasthenic syndrome characterized by autosomal dominant inheritance of postsynaptic neuromuscular junction defects resulting in prolonged synaptic currents and early-onset progressive muscle weakness that has_material_basis_in heterozygous mutation in the CHRND gene on chromosome 2q37.
  • synonyms:
  • 616321,
  • OMIM:616321,
  • congenital myasthenic syndrome 3A, slow-channel,
  • CMS3A
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents