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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

MIM:
MIM:162100 - AMYOTROPHY, HEREDITARY NEURALGIC; HNA

Other Model Organisms: Alliance, 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)