Search Ontology:
Human Disease
amyotrophic neuralgia
- Term ID
- DOID:10383
- Synonyms
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- neuralgic amyotrophy
- 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. https://medlineplus.gov/genetics/condition/hereditary-neuralgic-amyotrophy/
- References
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- ICD10CM:G54.5
- ICD9CM:353.5
- MESH:D020968
- MIM:162100
- SNOMEDCT_US_2023_03_01:3548001
- UMLS_CUI:C1510479
- Ontology
- Human Disease ( DOID:10383 )
- is a type of
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Genes Involved
Zebrafish Models