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Echinobase
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 (disorder), neuralgic amyotrophy

Echinobase Genes :


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)