DISEASES

Disease-gene associations mined from literature

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