amyotrophic neuralgia
Information
- Disease name
- amyotrophic neuralgia
- Disease ID
- DOID:10383
- Description
- "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." [url:https\://medlineplus.gov/genetics/condition/hereditary-neuralgic-amyotrophy/]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:3690
- Cross Reference ID (Disease Ontology)
- ICD10CM:G54.5
- Cross Reference ID (Disease Ontology)
- ICD9CM:353.5
- Cross Reference ID (Disease Ontology)
- MESH:D020968
- Cross Reference ID (Disease Ontology)
- MIM:162100
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:3548001
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C1510479
- Exact Synonym (Disease Ontology)
- neuralgic amyotrophy