Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:10383 - amyotrophic neuralgia

Disease Ontology Definition: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: neuralgic amyotrophy, neuralgic amyotrophy (disorder),

Xenbase Genes : septin9

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008076 - amyotrophic neuralgia


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), brachial plexus neuropathy (is_a)