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Statements

Subject Item

_:vb50946916

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n6:IAO_0000115

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A brachial plexus neuropathy that is characterized by acute, recurrent episodes of brachial plexus neuropathy with muscle weakness and atrophy preceded by severe pain in the affected arm, and that has_material_basis_in heterozygous mutation in the SEPT9 gene on chromosome 17q25.

obo:hasDbXref

url:https://medlineplus.gov/genetics/condition/hereditary-neuralgic-amyotrophy/