FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term amyotrophic neuralgia ID (Ontology) DOID:10383 (Human Disease)
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.
Also Known As "neuralgic amyotrophy"
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 Genes
 amyotrophic neuralgia       4
 for disease ribbon | amyotrophic neuralgia       4
 model of | amyotrophic neuralgia       4
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
neuropathy                      |
 |__brachial plexus neuropathy__|
                                amyotrophic neuralgia  4 rec.
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Is a autosomal dominant disease
brachial plexus neuropathy
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Synonyms
  • "neuralgic amyotrophy" EXACT
Secondary IDs
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ICD10CM:G54.5
ICD9CM:353.5
MESH:D020968
MIM:162100
SNOMEDCT_US_2023_03_01:3548001
UMLS_CUI:C1510479