Human genes for amyotrophic neuralgia
Amyotrophic neuralgia [DOID:10383]
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.
Synonyms: amyotrophic neuralgia, amyotrophic neuralgias, DOID:10383, neuralgic amyotrophy, neuralgic amyotrophies
Linkouts: OMIM