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amyotrophic neuralgia

Disease Summary
Associated Targets (1)
Tchem

1


GARD Rare
Mondo Description An autosomal dominant form of recurrent focal neuropathy characterized clinically by acute, recurrent episodes of brachial plexus neuropathy with muscle weakness and atrophy preceded by severe pain in the affected arm.
Uniprot Description Autosomal dominant form of recurrent focal neuropathy characterized clinically by acute, recurrent episodes of brachial plexus neuropathy with muscle weakness and atrophy preceded by severe pain in the affected arm. HNA is triggered by environmental factors such as infection or parturition.
Mondo Term and Equivalent IDs
MONDO:0008076:  amyotrophic neuralgia
GARD:0003955: 
ICD9:353.5: 
SCTID:26609002: